Biomimetic scaffolds for regeneration of volumetric muscle loss in skeletal muscle injuries

Acta Biomaterialia

Volumn 25, Issue , 2015, Pages 2-15

  Grasman, Jonathan M ^a,b   Zayas, Michelle J ^a   Page, Raymond L ^a,b   Pins, George D ^a,b  

^a Worcester Polytechnic Institute   (United States)

^b WORCESTER POLYTECHNIC INSTITUTE   (United States)

Author keywords

Biomaterials; Fibrin; Microthreads; Skeletal muscle regeneration; Tissue engineering

Indexed keywords

ACCIDENTS; BIOMIMETICS; BUILDINGS; COLLAGEN; REPAIR; SCAFFOLDS (BIOLOGY); TISSUE REGENERATION;

BIOMIMETIC SCAFFOLDS; FIBRIN; MICROTHREAD; MUSCLE INJURIES; MUSCLE REGENERATION; SKELETAL MUSCLE; SKELETAL MUSCLE REGENERATION; SOFT TISSUE; TISSUES ENGINEERINGS; VOLUMETRICS;

MUSCLE;

POLYMER; BIOMIMETIC MATERIAL;

ANGIOGENESIS; BASEMENT MEMBRANE; BIOMIMETICS; ENDOTHELIUM CELL; EXTRACELLULAR MATRIX; HUMAN; MACROPHAGE; MUSCLE CELL; MUSCLE DEVELOPMENT; MUSCLE INJURY; MUSCLE REGENERATION; NONHUMAN; PARACRINE SIGNALING; PHENOTYPE; PRIORITY JOURNAL; REVIEW; TISSUE ENGINEERING; TISSUE REGENERATION; TISSUE SCAFFOLD; VOLUMETRY; ANIMAL; CHEMISTRY; DISEASE MODEL; DRUG EFFECTS; INJURIES; PATHOLOGY; REGENERATION; SKELETAL MUSCLE;

ANIMALS; BIOMIMETIC MATERIALS; DISEASE MODELS, ANIMAL; HUMANS; MUSCLE, SKELETAL; REGENERATION; TISSUE ENGINEERING; TISSUE SCAFFOLDS;

EID: 84940895935     PISSN: 17427061     EISSN: 18787568     Source Type: Journal    
DOI: 10.1016/j.actbio.2015.07.038     Document Type: Review

References (224)

1. B.F. Grogan, and J.R. Hsu Volumetric muscle loss J. Am. Acad. Ortho. Surg. 19 Suppl. 1 2011 S35 S37
2. S.B. Charge, and M.A. Rudnicki Cellular and molecular regulation of muscle regeneration Physiol. Rev. 84 2004 209 238
3. A.J. Quintero, V.J. Wright, F.H. Fu, and J. Huard Stem cells for the treatment of skeletal muscle injury Clin. Sports Med. 28 2009 1 11
4. W. Bian, and N. Bursac Tissue engineering of functional skeletal muscle: challenges and recent advances IEEE Eng. Med. Biol. Mag. 27 2008 109 113
5. P. Counsel, and W. Breidahl Muscle injuries of the lower leg Semin. Musculoskeletal Radiol. 14 2010 162 175
6. 2009 Report of the 2008 Statistics of Plastic Surgery Statistics, American Society of Plastic Surgeons, 2009.
7. A. Eckardt Microsurgical reconstruction in the head and neck region: an 18-year experience with 500 consecutive cases J. Cranio-Maxillofacial Surg. 31 2003 197 201
8. B.D. Owens, J.F. Kragh Jr., J. Macaitis, S.J. Svoboda, and J.C. Wenke Characterization of extremity wounds in operation Iraqi freedom and operation enduring freedom J. Orthop. Trauma 21 2007 254 257
9. B.D. Owens, J.F. Kragh Jr., J.C. Wenke, J. Macaitis, C.E. Wade, and J.B. Holcomb Combat wounds in operation Iraqi freedom and operation enduring freedom J. Trauma 64 2008 295 299
10. N.J. Turner, and S.F. Badylak Regeneration of skeletal muscle Cell Tissue Res. 347 2012 759 774
11. G.S. Lynch, J.D. Schertzer, and J.G. Ryall Anabolic agents for improving muscle regeneration and function after injury Clin. Exp. Pharmacol. Physiol. 35 2008 852 858
12. T.A. Jarvinen, T.L. Jarvinen, M. Kaariainen, V. Aarimaa, S. Vaittinen, H. Kalimo, and et al. Muscle injuries: optimising recovery Best Pract. Res. Clin. Rheumatol. 21 2007 317 331
13. T.A. Jarvinen, T.L. Jarvinen, M. Kaariainen, H. Kalimo, and M. Jarvinen Muscle injuries: biology and treatment Am. J. Sports Med. 33 2005 745 764
14. T.A. Jarvinen, M. Kaariainen, M. Jarvinen, and H. Kalimo Muscle strain injuries Curr. Opin. Rheumatol. 12 2000 155 161
15. P. Kannus, J. Parkkari, T.L. Jarvinen, T.A. Jarvinen, and M. Jarvinen Basic science and clinical studies coincide: active treatment approach is needed after a sports injury 13 2003 150 154
16. P. De Coppi, S. Bellini, M.T. Conconi, M. Sabatti, E. Simonato, P.G. Gamba, and et al. Myoblast-acellular skeletal muscle matrix constructs guarantee a long-term repair of experimental full-thickness abdominal wall defects Tissue Eng. 12 2006 1929 1936
17. B. Bianchi, C. Copelli, S. Ferrari, A. Ferri, and E. Sesenna Free flaps: outcomes and complications in head and neck reconstructions J. Craniomaxillofac. Surg. 37 2009 438 442
18. V.J. Mase Jr., J.R. Hsu, S.E. Wolf, J.C. Wenke, D.G. Baer, J. Owens, and et al. Clinical application of an acellular biologic scaffold for surgical repair of a large, traumatic quadriceps femoris muscle defect Orthopedics 33 2010 511
19. R. Floriano, B. Peral, R. Alvarez, and A. Verrier Microvascular free flaps in head and neck reconstruction. Report of 71 cases J. Cranio-Maxillofacial Surg. 34 2006 90
20. J.P. Beier, J. Stern-Straeter, V.T. Foerster, U. Kneser, G.B. Stark, and A.D. Bach Tissue engineering of injectable muscle: three-dimensional myoblast-fibrin injection in the syngeneic rat animal model Plast. Reconstr. Surg. 118 2006 1113 1121 (discussion 22-24)
21. J. Huard, Y. Li, and F.H. Fu Muscle injuries and repair: current trends in research J. Bone Joint Surg. Am. 84-A 2002 822 832
22. H. Yin, F. Price, and M.A. Rudnicki Satellite cells and the muscle stem cell niche Physiol. Rev. 93 2013 23 67
23. S. Grefte, A.M. Kuijpers-Jagtman, R. Torensma, and J.W. Von den Hoff Skeletal muscle development and regeneration Stem Cells Dev. 16 2007 857 868
24. S. Schiaffino, and C. Reggiani Fiber types in mammalian skeletal muscles Physiol. Rev. 91 2011 1447 1531
25. J.R. Sanes The basement membrane/basal lamina of skeletal muscle J. Biol. Chem. 278 2003 12601 12604
26. M. Cassano, M. Quattrocelli, S. Crippa, I. Perini, F. Ronzoni, and M. Sampaolesi Cellular mechanisms and local progenitor activation to regulate skeletal muscle mass J. Muscle Res. Cell Motil. 30 2009 243 253
27. S.G. Velleman The role of the extracellular matrix in skeletal muscle development Poult. Sci. 78 1999 778 784
28. M.T. Wolf, K.A. Daly, J.E. Reing, and S.F. Badylak Biologic scaffold composed of skeletal muscle extracellular matrix Biomaterials 33 2012 2916 2925
29. J.E. Morgan, and T.A. Partridge Muscle satellite cells Int. J. Biochem. Cell Biol. 35 2003 1151 1156
30. P.S. Zammit, T.A. Partridge, and Z. Yablonka-Reuveni The skeletal muscle satellite cell: the stem cell that came in from the cold J. Histochem. Cytochem. 54 2006 1177 1191
31. J.D. Starkey, M. Yamamoto, S. Yamamoto, and D.J. Goldhamer Skeletal muscle satellite cells are committed to myogenesis and do not spontaneously adopt nonmyogenic fates J. Histochem. Cytochem. 59 2011 33 46
32. B.D. Cosgrove, A. Sacco, P.M. Gilbert, and H.M. Blau A home away from home: challenges and opportunities in engineering in vitro muscle satellite cell niches Differentiation 78 2009 185 194
33. J.G. Tidball Mechanisms of muscle injury, repair, and regeneration Compr. Physiol. 1 2011 2029 2062
34. S. Bodine-Fowler Skeletal muscle regeneration after injury: an overview J. Voice 8 1994 53 62
35. N. Kimura, S. Hirata, N. Miyasaka, K. Kawahata, and H. Kohsaka Injury and subsequent regeneration of muscles for activation of local innate immunity to facilitate the development and relapse of autoimmune myositis in C57BL/6 mice Arthritis Rheumatol. 67 2015 1107 1116
36. T. Hurme, H. Kalimo, M. Lehto, and M. Jarvinen Healing of skeletal muscle injury: an ultrastructural and immunohistochemical study Med. Sci. Sports Exerc. 23 1991 801 810
37. S. Carpenter, and G. Karpati Segmental necrosis and its demarcation in experimental micropuncture injury of skeletal muscle fibers J. Neuropathol. Exp. Neurol. 48 1989 154 170
38. J.G. Tidball, and S.A. Villalta Regulatory interactions between muscle and the immune system during muscle regeneration Am. J. Physiol. Regul. Integr. Comp. Physiol. 298 2010 R1173 R1187
39. R. Tatsumi Mechano-biology of skeletal muscle hypertrophy and regeneration: possible mechanism of stretch-induced activation of resident myogenic stem cells Anim. Sci. J. (Nihon chikusan Gakkaiho) 81 2010 11 20
40. R. Tatsumi, A. Hattori, Y. Ikeuchi, J.E. Anderson, and R.E. Allen Release of hepatocyte growth factor from mechanically stretched skeletal muscle satellite cells and role of pH and nitric oxide Mol. Biol. Cell 13 2002 2909 2918
41. R. Tatsumi, X. Liu, A. Pulido, M. Morales, T. Sakata, S. Dial, and et al. Satellite cell activation in stretched skeletal muscle and the role of nitric oxide and hepatocyte growth factor Am. J. Physiol. Cell Physiol. 290 2006 C1487 C1494
42. M. Hara, K. Tabata, T. Suzuki, M.K. Do, W. Mizunoya, M. Nakamura, and et al. Calcium influx through a possible coupling of cation channels impacts skeletal muscle satellite cell activation in response to mechanical stretch Am. J. Physiol. Cell Physiol. 302 2012 C1741 C1750
43. J.G. Cannon, and B.A. St Pierre Cytokines in exertion-induced skeletal muscle injury Mol. Cell. Biochem. 179 1998 159 167
44. X. Liu, G. Wu, D. Shi, R. Zhu, H. Zeng, B. Cao, and et al. Effects of nitric oxide on notexin-induced muscle inflammatory responses Int. J. Biol. Sci. 11 2015 156 167
45. Y. Wang, M. Wehling-Henricks, G. Samengo, and J.G. Tidball Increases of M2a macrophages and fibrosis in aging muscle are influenced by bone marrow aging and negatively regulated by muscle-derived nitric oxide Aging Cell 2015
46. S.A. Villalta, B. Deng, C. Rinaldi, M. Wehling-Henricks, and J.G. Tidball IFN-gamma promotes muscle damage in the mdx mouse model of Duchenne muscular dystrophy by suppressing M2 macrophage activation and inhibiting muscle cell proliferation J. Immunol. 187 2011 5419 5428
47. B. Deng, M. Wehling-Henricks, S.A. Villalta, Y. Wang, and J.G. Tidball IL-10 triggers changes in macrophage phenotype that promote muscle growth and regeneration J. Immunol. 189 2012 3669 3680
48. S.A. Villalta, C. Rinaldi, B. Deng, G. Liu, B. Fedor, and J.G. Tidball Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype Hum. Mol. Genet. 20 2011 790 805
49. R. Tatsumi, S.M. Sheehan, H. Iwasaki, A. Hattori, and R.E. Allen Mechanical stretch induces activation of skeletal muscle satellite cells in vitro Exp. Cell Res. 267 2001 107 114
50. R. Gal-Levi, Y. Leshem, S. Aoki, T. Nakamura, and O. Halevy Hepatocyte growth factor plays a dual role in regulating skeletal muscle satellite cell proliferation and differentiation Biochim. Biophys. Acta 1402 1998 39 51
51. R. Tatsumi, and R.E. Allen Active hepatocyte growth factor is present in skeletal muscle extracellular matrix Muscle Nerve 30 2004 654 658
52. R. Tatsumi, J.E. Anderson, C.J. Nevoret, O. Halevy, and R.E. Allen HGF/SF is present in normal adult skeletal muscle and is capable of activating satellite cells Dev. Biol. 194 1998 114 128
53. J.E. Anderson, and A.C. Wozniak Satellite cell activation on fibers: modeling events in vivo - an invited review Can. J. Physiol. Pharmacol. 82 2004 300 310
54. S. Hayashi, H. Aso, K. Watanabe, H. Nara, M.T. Rose, S. Ohwada, and et al. Sequence of IGF-I, IGF-II, and HGF expression in regenerating skeletal muscle Histochem. Cell Biol. 122 2004 427 434
55. O. deLapeyriere, V. Ollendorff, J. Planche, M.O. Ott, S. Pizette, F. Coulier, and et al. Expression of the Fgf6 gene is restricted to developing skeletal muscle in the mouse embryo Development 118 1993 601 611
56. T. Floss, H.H. Arnold, and T. Braun A role for FGF-6 in skeletal muscle regeneration Genes Dev. 11 1997 2040 2051
57. D.D. Cornelison, M.S. Filla, H.M. Stanley, A.C. Rapraeger, and B.B. Olwin Syndecan-3 and syndecan-4 specifically mark skeletal muscle satellite cells and are implicated in satellite cell maintenance and muscle regeneration Dev. Biol. 239 2001 79 94
58. S.M. Sheehan, R. Tatsumi, C.J. Temm-Grove, and R.E. Allen HGF is an autocrine growth factor for skeletal muscle satellite cells in vitro Muscle Nerve 23 2000 239 245
59. D. Montarras, J. Morgan, C. Collins, F. Relaix, S. Zaffran, A. Cumano, and et al. Direct isolation of satellite cells for skeletal muscle regeneration Science 309 2005 2064 2067
60. D.J. Watt, J.E. Morgan, M.A. Clifford, and T.A. Partridge The movement of muscle precursor cells between adjacent regenerating muscles in the mouse Anat. Embryol. 175 1987 527 536
61. J.D. Rosenblatt, D. Yong, and D.J. Parry Satellite cell activity is required for hypertrophy of overloaded adult rat muscle Muscle Nerve 17 1994 608 613
62. A. Sacco, R. Doyonnas, P. Kraft, S. Vitorovic, and H.M. Blau Self-renewal and expansion of single transplanted muscle stem cells Nature 456 2008 502 506
63. C.A. Collins, I. Olsen, P.S. Zammit, L. Heslop, A. Petrie, T.A. Partridge, and et al. Stem cell function, self-renewal, and behavioral heterogeneity of cells from the adult muscle satellite cell niche Cell 122 2005 289 301
64. R.N. Cooper, S. Tajbakhsh, V. Mouly, G. Cossu, M. Buckingham, and G.S. Butler-Browne In vivo satellite cell activation via Myf5 and MyoD in regenerating mouse skeletal muscle J. Cell Sci. 112 Pt 17 1999 2895 2901
65. D.D. Cornelison, and B.J. Wold Single-cell analysis of regulatory gene expression in quiescent and activated mouse skeletal muscle satellite cells Dev. Biol. 191 1997 270 283
66. Z. Yablonka-Reuveni, K. Day, A. Vine, and G. Shefer Defining the transcriptional signature of skeletal muscle stem cells J. Anim. Sci. 86 2008 E207 E216
67. P. Zammit Kinetics of myoblast proliferation show that resident satellite cells are competent to fully regenerate skeletal muscle fibers Exp. Cell Res. 281 2002 39 49
68. Z. Yablonka-Reuveni, and A.J. Rivera Temporal expression of regulatory and structural muscle proteins during myogenesis of satellite cells on isolated adult rat fibers Dev. Biol. 164 1994 588 603
69. Y. Leshem, D.B. Spicer, R. Gal-Levi, and O. Halevy Hepatocyte growth factor (HGF) inhibits skeletal muscle cell differentiation: a role for the bHLH protein twist and the cdk inhibitor p27 J. Cell. Physiol. 184 2000 101 109
70. S. Kastner, M.C. Elias, A.J. Rivera, and Z. Yablonka-Reuveni Gene expression patterns of the fibroblast growth factors and their receptors during myogenesis of rat satellite cells J. Histochem. Cytochem. 48 2000 1079 1096
71. C. O'Reilly, B. McKay, S. Phillips, M. Tarnopolsky, and G. Parise Hepatocyte growth factor (HGF) and the satellite cell response following muscle lengthening contractions in humans Muscle Nerve 38 2008 1434 1442
72. S. Suzuki, K. Yamanouchi, C. Soeta, Y. Katakai, R. Harada, K. Naito, and et al. Skeletal muscle injury induces hepatocyte growth factor expression in spleen Biochem. Biophys. Res. Commun. 292 2002 709 714
73. J. Menetrey, C. Kasemkijwattana, C.S. Day, P. Bosch, M. Vogt, F.H. Fu, and et al. Growth factors improve muscle healing in vivo J. Bone Joint Sur. Br. 82 2000 131 137
74. L. Pelosi, C. Giacinti, C. Nardis, G. Borsellino, E. Rizzuto, C. Nicoletti, and et al. Local expression of IGF-1 accelerates muscle regeneration by rapidly modulating inflammatory cytokines and chemokines FASEB J. 21 2007 1393 1402
75. J.C. Engert, E.B. Berglund, and N. Rosenthal Proliferation precedes differentiation in IGF-I-stimulated myogenesis J. Cell Biol. 135 1996 431 440
76. J.R. Florini, D.Z. Ewton, and S.A. Coolican Growth hormone and the insulin-like growth factor system in myogenesis Endocr. Rev. 17 1996 481 517
77. J.R. Florini, D.Z. Ewton, and K.A. Magri Hormones, growth factors, and myogenic differentiation Annu. Rev. Physiol. 53 1991 201 216
78. S.A. Coolican, D.S. Samuel, D.Z. Ewton, F.J. McWade, and J.R. Florini The mitogenic and myogenic actions of insulin-like growth factors utilize distinct signaling pathways J. Biol. Chem. 272 1997 6653 6662
79. C.W. Smith, J.G. Klaasmeyer, T.L. Woods, and S.J. Jones Effects of IGF-I, IGF-II, bFGF and PDGF on the initiation of mRNA translation in C2C12 myoblasts and differentiating myoblasts Tissue Cell 31 1999 403 412
80. H.H. Vandenburgh, P. Karlisch, J. Shansky, and R. Feldstein Insulin and IGF-I induce pronounced hypertrophy of skeletal myofibers in tissue culture Am. J. Physiol. 260 1991 C475 C484
81. J.P. Lefaucheur, and A. Sebille Muscle regeneration following injury can be modified in vivo by immune neutralization of basic fibroblast growth factor, transforming growth factor beta 1 or insulin-like growth factor I J. Neuroimmunol. 57 1995 85 91
82. H.L. Keller, B. St Pierre Schneider, L.A. Eppihimer, and J.G. Cannon Association of IGF-I and IGF-II with myofiber regeneration in vivo Muscle Nerve 22 1999 347 354
83. M.V. Chakravarthy, B.S. Davis, and F.W. Booth IGF-I restores satellite cell proliferative potential in immobilized old skeletal muscle J. Appl. Physiol. 89 2000 1365 1379
84. T.J. Hawke, and D.J. Garry Myogenic satellite cells: physiology to molecular biology J. Appl. Physiol. 91 2001 534 551
85. J. Tonkin, L. Temmerman, R.D. Sampson, E. Gallego-Colon, L. Barberi, D. Bilbao, and et al. Monocyte/macrophage-derived IGF-1 orchestrates murine skeletal muscle regeneration and modulates autocrine polarization Mol. Ther. 2015
86. W.M. Wood, S. Etemad, M. Yamamoto, and D.J. Goldhamer MyoD-expressing progenitors are essential for skeletal myogenesis and satellite cell development Dev. Biol. 384 2013 114 127
87. M.M. Murphy, J.A. Lawson, S.J. Mathew, D.A. Hutcheson, and G. Kardon Satellite cells, connective tissue fibroblasts and their interactions are crucial for muscle regeneration Development 138 2011 3625 3637
88. M. Lehto, M. Jarvinen, and O. Nelimarkka Scar formation after skeletal muscle injury. A histological and autoradiographical study in rats Arch. Ortho. Traumatic Surg. Archiv fur orthopadische und Unfall-Chirurgie 104 1986 366 370
89. M.A. Machingal, B.T. Corona, T.J. Walters, V. Kesireddy, C.N. Koval, A. Dannahower, and et al. A tissue-engineered muscle repair construct for functional restoration of an irrecoverable muscle injury in a murine model Tissue Eng. Part A 17 2011 2291 2303
90. B.T. Corona, X. Wu, C.L. Ward, J.S. McDaniel, C.R. Rathbone, and T.J. Walters The promotion of a functional fibrosis in skeletal muscle with volumetric muscle loss injury following the transplantation of muscle-ECM Biomaterials 34 2013 3324 3335
91. R.L. Page, C. Malcuit, L. Vilner, I. Vojtic, S. Shaw, E. Hedblom, and et al. Restoration of skeletal muscle defects with adult human cells delivered on fibrin microthreads Tissue Eng. Part A 17 2011 2629 2640
92. M. Lehto, V.C. Duance, and D. Restall Collagen and fibronectin in a healing skeletal muscle injury. An immunohistological study of the effects of physical activity on the repair of injured gastrocnemius muscle in the rat J. Bone Joint Surg. Br. 67 1985 820 828
93. C. Borselli, H. Storrie, F. Benesch-Lee, D. Shvartsman, C. Cezar, J.W. Lichtman, and et al. Functional muscle regeneration with combined delivery of angiogenesis and myogenesis factors Proc. Natl. Acad. Sci. USA 107 2010 3287 3292
94. M.L. Springer, A.S. Chen, P.E. Kraft, M. Bednarski, and H.M. Blau VEGF gene delivery to muscle: potential role for vasculogenesis in adults Mol. Cell 2 1998 549 558
95. C. Christov, F. Chretien, R. Abou-Khalil, G. Bassez, G. Vallet, F.J. Authier, and et al. Muscle satellite cells and endothelial cells: close neighbors and privileged partners Mol. Biol. Cell 18 2007 1397 1409
96. R. Mounier, F. Chretien, and B. Chazaud Blood vessels and the satellite cell niche Curr. Top. Dev. Biol. 96 2011 121 138
97. P. Caroni, C. Schneider, M.C. Kiefer, and J. Zapf Role of muscle insulin-like growth factors in nerve sprouting: suppression of terminal sprouting in paralyzed muscle by IGF-binding protein 4 J. Cell Biol. 125 1994 893 902
98. G. Liu, R.A. Pareta, R. Wu, Y. Shi, X. Zhou, H. Liu, and et al. Skeletal myogenic differentiation of urine-derived stem cells and angiogenesis using microbeads loaded with growth factors Biomaterials 34 2013 1311 1326
99. M.S. Kim, S.H. Bhang, H.S. Yang, N.G. Rim, I. Jun, S.I. Kim, and et al. Development of functional fibrous matrices for the controlled release of basic fibroblast growth factor to improve therapeutic angiogenesis Tissue Eng. Part A 16 2010 2999 3010
100. E. Fathi, S.M. Nassiri, N. Atyabi, S.H. Ahmadi, M. Imani, R. Farahzadi, and et al. Induction of angiogenesis via topical delivery of basic-fibroblast growth factor from polyvinyl alcohol-dextran blend hydrogel in an ovine model of acute myocardial infarction J. Tissue Eng. Regener. Med. 7 2013 697 707
101. T. Nakamura, and S. Mizuno The discovery of hepatocyte growth factor (HGF) and its significance for cell biology, life sciences and clinical medicine Proc. Jan. Acad. Ser. B, Phys. Biol. Sci. 86 2010 588 610
102. R. Madonna, C. Cevik, M. Nasser, and R. De Caterina Hepatocyte growth factor: molecular biomarker and player in cardioprotection and cardiovascular regeneration Thromb. Haemost. 107 2012 656 661
103. T.A. Jarvinen, M. Jarvinen, and H. Kalimo Regeneration of injured skeletal muscle after the injury Muscles Ligaments Tendons J. 3 2013 337 345
104. J. Stern-Straeter, F. Riedel, G. Bran, K. Hormann, and U.R. Goessler Advances in skeletal muscle tissue engineering In Vivo 21 2007 435 444
105. M. Koning, M.C. Harmsen, M.J. van Luyn, and P.M. Werker Current opportunities and challenges in skeletal muscle tissue engineering J. Tissue Eng. Regener. Med. 3 2009 407 415
106. M.T. Wolf, C.L. Dearth, S.B. Sonnenberg, E.G. Loboa, and S.F. Badylak Naturally derived and synthetic scaffolds for skeletal muscle reconstruction Adv. Drug Deliv. Rev. 84 2015 208 221
107. J.P. Mertens, K.B. Sugg, J.D. Lee, and L.M. Larkin Engineering muscle constructs for the creation of functional engineered musculoskeletal tissue Regener. Med. 9 2014 89 100
108. H. Liao, and G.Q. Zhou Development and progress of engineering of skeletal muscle tissue Tissue Eng. Part B Rev. 15 2009 319 331
109. J.S. Choi, S.J. Lee, G.J. Christ, A. Atala, and J.J. Yoo The influence of electrospun aligned poly(epsilon-caprolactone)/collagen nanofiber meshes on the formation of self-aligned skeletal muscle myotubes Biomaterials 29 2008 2899 2906
110. R. Shah, A.C. Sinanan, J.C. Knowles, N.P. Hunt, and M.P. Lewis Craniofacial muscle engineering using a 3-dimensional phosphate glass fibre construct Biomaterials 26 2005 1497 1505
111. J.P. Beier, D. Klumpp, M. Rudisile, R. Dersch, J.H. Wendorff, O. Bleiziffer, and et al. Collagen matrices from sponge to nano: new perspectives for tissue engineering of skeletal muscle BMC Biotechnol. 9 2009 34
112. K.G. Cornwell, B.R. Downing, and G.D. Pins Characterizing fibroblast migration on discrete collagen threads for applications in tissue regeneration J. Biomed. Mater. Res. A 71 2004 55 62
113. V. Kroehne, I. Heschel, F. Schugner, D. Lasrich, J.W. Bartsch, and H. Jockusch Use of a novel collagen matrix with oriented pore structure for muscle cell differentiation in cell culture and in grafts J. Cell Mol. Med. 12 2008 1640 1648
114. J.J. Norman, and T.A. Desai Control of cellular organization in three dimensions using a microfabricated polydimethylsiloxane-collagen composite tissue scaffold Tissue Eng. 11 2005 378 386
115. M.R. Williamson, E.F. Adams, and A.G. Coombes Gravity spun polycaprolactone fibres for soft tissue engineering: interaction with fibroblasts and myoblasts in cell culture Biomaterials 27 2006 1019 1026
116. M.P. Lutolf, and J.A. Hubbell Synthetic biomaterials as instructive extracellular microenvironments for morphogenesis in tissue engineering Nat. Biotechnol. 23 2005 47 55
117. D.J. Geer, D.D. Swartz, and S.T. Andreadis Biomimetic delivery of keratinocyte growth factor upon cellular demand for accelerated wound healing in vitro and in vivo Am. J. Pathol. 167 2005 1575 1586
118. D.W. Hutmacher Scaffold design and fabrication technologies for engineering tissues - state of the art and future perspectives J. Biomater. Sci. Polym. Ed. 12 2001 107 124
119. H. Vandenburgh, M. Del Tatto, J. Shansky, J. Lemaire, A. Chang, F. Payumo, and et al. Tissue-engineered skeletal muscle organoids for reversible gene therapy Hum. Gene Ther. 7 1996 2195 2200
120. H.H. Vandenburgh, S. Hatfaludy, P. Karlisch, and J. Shansky Mechanically induced alterations in cultured skeletal muscle growth J. Biomech. 24 Suppl. 1 1991 91 99
121. R.G. Dennis, P.E. Kosnik 2nd, M.E. Gilbert, and J.A. Faulkner Excitability and contractility of skeletal muscle engineered from primary cultures and cell lines Am. J. Physiol. Cell Physiol. 280 2001 C288 C295
122. Y.C. Huang, R.G. Dennis, L. Larkin, and K. Baar Rapid formation of functional muscle in vitro using fibrin gels J. Appl. Physiol. 98 2005 706 713
123. P.E. Kosnik, J.A. Faulkner, and R.G. Dennis Functional development of engineered skeletal muscle from adult and neonatal rats Tissue Eng. 7 2001 573 584
124. M. Juhas, G.C. Engelmayr Jr., A.N. Fontanella, G.M. Palmer, and N. Bursac Biomimetic engineered muscle with capacity for vascular integration and functional maturation in vivo Proc. Natl. Acad. Sci. USA 111 2014 5508 5513
125. H. Vandenburgh High-content drug screening with engineered musculoskeletal tissues Tissue Eng. Part B Rev. 16 2010 55 64
126. H. Vandenburgh, J. Shansky, F. Benesch-Lee, V. Barbata, J. Reid, L. Thorrez, and et al. Drug-screening platform based on the contractility of tissue-engineered muscle Muscle Nerve 37 2008 438 447
127. H. Vandenburgh, J. Shansky, F. Benesch-Lee, K. Skelly, J.M. Spinazzola, Y. Saponjian, and et al. Automated drug screening with contractile muscle tissue engineered from dystrophic myoblasts FASEB J. 23 2009 3325 3334
128. R.G. Dennis, and P.E. Kosnik 2nd Excitability and isometric contractile properties of mammalian skeletal muscle constructs engineered in vitro In Vitro Cell. Dev. Biol. Anim. 36 2000 327 335
129. S. Carosio, L. Barberi, E. Rizzuto, C. Nicoletti, Z. Del Prete, and A. Musaro Generation of eX vivo-vascularized Muscle Engineered Tissue (X-MET) Sci. Rep. 3 2013 1420
130. G.H. Borschel, D.E. Dow, R.G. Dennis, and D.L. Brown Tissue-engineered axially vascularized contractile skeletal muscle Plast. Reconstr. Surg. 117 2006 2235 2242
131. M.L. Williams, T.Y. Kostrominova, E.M. Arruda, and L.M. Larkin Effect of implantation on engineered skeletal muscle constructs J. Tissue Eng. Regener. Med. 7 2013 434 442
132. K.W. VanDusen, B.C. Syverud, M.L. Williams, J.D. Lee, and L.M. Larkin Engineered skeletal muscle units for repair of volumetric muscle loss in the tibialis anterior muscle of a rat Tissue Eng. Part A 20 2014 2920 2930
133. A.K. Saxena, J. Marler, M. Benvenuto, G.H. Willital, and J.P. Vacanti Skeletal muscle tissue engineering using isolated myoblasts on synthetic biodegradable polymers: preliminary studies Tissue Eng. 5 1999 525 531
134. B.M. Sicari, J.P. Rubin, C.L. Dearth, M.T. Wolf, F. Ambrosio, M. Boninger, and et al. An acellular biologic scaffold promotes skeletal muscle formation in mice and humans with volumetric muscle loss Sci. Transl. Med. 6 2014 234ra58
135. L. Thorrez, J. Shansky, L. Wang, L. Fast, T. VandenDriessche, M. Chuah, and et al. Growth, differentiation, transplantation and survival of human skeletal myofibers on biodegradable scaffolds Biomaterials 29 2008 75 84
136. E. Hill, T. Boontheekul, and D.J. Mooney Designing scaffolds to enhance transplanted myoblast survival and migration Tissue Eng. 12 2006 1295 1304
137. J. Stern-Straeter, G. Bran, F. Riedel, A. Sauter, K. Hormann, and U.R. Goessler Characterization of human myoblast cultures for tissue engineering Int. J. Mol. Med. 21 2008 49 56
138. A.K. Saxena, G.H. Willital, and J.P. Vacanti Vascularized three-dimensional skeletal muscle tissue-engineering Bio-Med. Mater. Eng. 11 2001 275 281
139. E.M. Cronin, F.A. Thurmond, R. Bassel-Duby, R.S. Williams, W.E. Wright, K.D. Nelson, and et al. Protein-coated poly(l-lactic acid) fibers provide a substrate for differentiation of human skeletal muscle cells J. Biomed. Mater. Res. A 69 2004 373 381
140. A. Lesman, J. Koffler, R. Atlas, Y.J. Blinder, Z. Kam, and S. Levenberg Engineering vessel-like networks within multicellular fibrin-based constructs Biomaterials 32 2011 7856 7869
141. M.E. Hoque, W.Y. San, F. Wei, S. Li, M.H. Huang, M. Vert, and et al. Processing of polycaprolactone and polycaprolactone-based copolymers into 3D scaffolds, and their cellular responses Tissue Eng. Part A 15 2009 3013 3024
142. M.S. Kim, I. Jun, Y.M. Shin, W. Jang, S.I. Kim, and H. Shin The development of genipin-crosslinked poly(caprolactone) (PCL)/gelatin nanofibers for tissue engineering applications Macromol. Biosci. 10 2010 91 100
143. I. Grizzi, H. Garreau, S. Li, and M. Vert Hydrolytic degradation of devices based on poly(dl-lactic acid) size-dependence Biomaterials 16 1995 305 311
144. S. Li Hydrolytic degradation characteristics of aliphatic polyesters derived from lactic and glycolic acids J. Biomed. Mater. Res. 48 1999 342 353
145. S. Ostrovidov, V. Hosseini, S. Ahadian, T. Fujie, S.P. Parthiban, M. Ramalingam, and et al. Skeletal muscle tissue engineering: methods to form skeletal myotubes and their applications Tissue Eng. Part B Rev. 20 2014 403 436
146. A. Tamayol, M. Akbari, N. Annabi, A. Paul, A. Khademhosseini, and D. Juncker Fiber-based tissue engineering: progress, challenges, and opportunities Biotechnol. Adv. 31 2013 669 687
147. T. Neumann, S.D. Hauschka, and J.E. Sanders Tissue engineering of skeletal muscle using polymer fiber arrays Tissue Eng. 9 2003 995 1003
148. A.G. Guex, D.L. Birrer, G. Fortunato, H.T. Tevaearai, and M.N. Giraud Anisotropically oriented electrospun matrices with an imprinted periodic micropattern: a new scaffold for engineered muscle constructs Biomed. Mater. 8 2013 021001
149. S. Sirivisoot, R. Pareta, and B.S. Harrison Protocol and cell responses in three-dimensional conductive collagen gel scaffolds with conductive polymer nanofibres for tissue regeneration Interface Focus 4 2014 20130050
150. S.H. Ku, S.H. Lee, and C.B. Park Synergic effects of nanofiber alignment and electroactivity on myoblast differentiation Biomaterials 33 2012 6098 6104
151. M.C. Chen, Y.C. Sun, and Y.H. Chen Electrically conductive nanofibers with highly oriented structures and their potential application in skeletal muscle tissue engineering Acta Biomater. 9 2013 5562 5572
152. D.M. Nelson, P.R. Baraniak, Z. Ma, J. Guan, N.S. Mason, and W.R. Wagner Controlled release of IGF-1 and HGF from a biodegradable polyurethane scaffold Pharm. Res. 28 2011 1282 1293
153. M.T. Wolf, C.A. Carruthers, C.L. Dearth, P.M. Crapo, A. Huber, O.A. Burnsed, and et al. Polypropylene surgical mesh coated with extracellular matrix mitigates the host foreign body response J. Biomed. Mater. Res. A 2013
154. C.X. Lam, D.W. Hutmacher, J.T. Schantz, M.A. Woodruff, and S.H. Teoh Evaluation of polycaprolactone scaffold degradation for 6 months in vitro and in vivo J. Biomed. Mater. Res. A 90 2009 906 919
155. W. Zhao, Y.M. Ju, G. Christ, A. Atala, J.J. Yoo, and S.J. Lee Diaphragmatic muscle reconstruction with an aligned electrospun poly(epsilon-caprolactone)/collagen hybrid scaffold Biomaterials 34 2013 8235 8240
156. W.S. Cobb, K.W. Kercher, and B.T. Heniford The argument for lightweight polypropylene mesh in hernia repair Surg. Innovations 12 2005 63 69
157. B. Klosterhalfen, K. Junge, and U. Klinge The lightweight and large porous mesh concept for hernia repair Expert Rev. Med. Devices 2 2005 103 117
158. F.S. Kamelger, R. Marksteiner, E. Margreiter, G. Klima, G. Wechselberger, S. Hering, and et al. A comparative study of three different biomaterials in the engineering of skeletal muscle using a rat animal model Biomaterials 25 2004 1649 1655
159. J. Yang, B. Jao, A.K. McNally, and J.M. Anderson In vivo quantitative and qualitative assessment of foreign body giant cell formation on biomaterials in mice deficient in natural killer lymphocyte subsets, mast cells, or the interleukin-4 receptoralpha and in severe combined immunodeficient mice J. Biomed. Mater. Res. A 102 2014 2017 2023
160. J.M. Anderson Exploiting the inflammatory response on biomaterials research and development J. Mater. Sci.-Mater. Med. 26 2015 121
161. S.F. Badylak, J.E. Valentin, A.K. Ravindra, G.P. McCabe, and A.M. Stewart-Akers Macrophage phenotype as a determinant of biologic scaffold remodeling Tissue Eng. Part A 14 2008 1835 1842
162. S.A. Hurd, N.M. Bhatti, A.M. Walker, B.M. Kasukonis, and J.C. Wolchok Development of a biological scaffold engineered using the extracellular matrix secreted by skeletal muscle cells Biomaterials 49 2015 9 17
163. S.F. Badylak The extracellular matrix as a biologic scaffold material Biomaterials 28 2007 3587 3593
164. S.F. Badylak, D.O. Freytes, and T.W. Gilbert Extracellular matrix as a biological scaffold material: structure and function Acta Biomater. 5 2009 1 13
165. B.N. Brown, and S.F. Badylak Extracellular matrix as an inductive scaffold for functional tissue reconstruction Transl. Res. 163 2014 268 285
166. D.M. Faulk, C.A. Carruthers, H.J. Warner, C.R. Kramer, J.E. Reing, L. Zhang, and et al. The effect of detergents on the basement membrane complex of a biologic scaffold material Acta Biomater. 10 2014 183 193
167. S.E. Gilpin, J.P. Guyette, G. Gonzalez, X. Ren, J.M. Asara, D.J. Mathisen, and et al. Perfusion decellularization of human and porcine lungs: bringing the matrix to clinical scale J. Heart Lung Transplant. 33 2014 298 308
168. T. Tsuchiya, J.L. Balestrini, J. Mendez, E.A. Calle, L. Zhao, and L.E. Niklason Influence of pH on extracellular matrix preservation during lung decellularization Tissue Eng. Part C Methods 20 2014 1028 1036
169. T. Tsuchiya, A. Sivarapatna, K. Rocco, A. Nanashima, T. Nagayasu, and L.E. Niklason Future prospects for tissue engineered lung transplantation: decellularization and recellularization-based whole lung regeneration Organogenesis 10 2014 196 207
170. M.H. Zheng, J. Chen, Y. Kirilak, C. Willers, J. Xu, and D. Wood Porcine small intestine submucosa (SIS) is not an acellular collagenous matrix and contains porcine DNA: possible implications in human implantation J. Biomed. Mater. Res. B Appl. Biomater. 73 2005 61 67
171. M.T. Conconi, P. De Coppi, S. Bellini, G. Zara, M. Sabatti, M. Marzaro, and et al. Homologous muscle acellular matrix seeded with autologous myoblasts as a tissue-engineering approach to abdominal wall-defect repair Biomaterials 26 2005 2567 2574
172. B.M. Sicari, V. Agrawal, B.F. Siu, C.J. Medberry, C.L. Dearth, N.J. Turner, and et al. A murine model of volumetric muscle loss and a regenerative medicine approach for tissue replacement Tissue Eng. Part A 18 2012 1941 1948
173. B. Perniconi, A. Costa, P. Aulino, L. Teodori, S. Adamo, and D. Coletti The pro-myogenic environment provided by whole organ scale acellular scaffolds from skeletal muscle Biomaterials 32 2011 7870 7882
174. M.T. Wolf, K.A. Daly, E.P. Brennan-Pierce, S.A. Johnson, C.A. Carruthers, A. D'Amore, and et al. A hydrogel derived from decellularized dermal extracellular matrix Biomaterials 33 2012 7028 7038
175. L. Wang, J.A. Johnson, D.W. Chang, and Q. Zhang Decellularized musculofascial extracellular matrix for tissue engineering Biomaterials 34 2013 2641 2654
176. E.K. Merritt, D.W. Hammers, M. Tierney, L.J. Suggs, T.J. Walters, and R.P. Farrar Functional assessment of skeletal muscle regeneration utilizing homologous extracellular matrix as scaffolding Tissue Eng. Part A 16 2010 1395 1405
177. X.K. Chen, and T.J. Walters Muscle-derived decellularised extracellular matrix improves functional recovery in a rat latissimus dorsi muscle defect model J. Plastic Reconstr. Aesthetic Surg. 66 2013 1750 1758
178. E.K. Merritt, M.V. Cannon, D.W. Hammers, L.N. Le, R. Gokhale, A. Sarathy, and et al. Repair of traumatic skeletal muscle injury with bone-marrow-derived mesenchymal stem cells seeded on extracellular matrix Tissue Eng. Part A 16 2010 2871 2881
179. B.T. Corona, M.A. Machingal, T. Criswell, M. Vadhavkar, A.C. Dannahower, C. Bergman, and et al. Further development of a tissue engineered muscle repair construct in vitro for enhanced functional recovery following implantation in vivo in a murine model of volumetric muscle loss injury Tissue Eng. Part A 18 2012 1213 1228
180. J.E. Valentin, N.J. Turner, T.W. Gilbert, and S.F. Badylak Functional skeletal muscle formation with a biologic scaffold Biomaterials 31 2010 7475 7484
181. B.T. Corona, C.L. Ward, H.B. Baker, T.J. Walters, and G.J. Christ Implantation of in vitro tissue engineered muscle repair constructs and bladder acellular matrices partially restore in vivo skeletal muscle function in a rat model of volumetric muscle loss injury Tissue Eng. Part A 20 2014 705 715
182. B.T. Corona, K. Garg, C.L. Ward, J.S. McDaniel, T.J. Walters, and C.R. Rathbone Autologous minced muscle grafts: a tissue engineering therapy for the volumetric loss of skeletal muscle Am. J. Physiol. Cell Physiol. 305 2013 C761 C775
183. E. Hill, T. Boontheekul, and D.J. Mooney Regulating activation of transplanted cells controls tissue regeneration Proc. Natl. Acad. Sci. USA 103 2006 2494 2499
184. G. Moon du, G. Christ, J.D. Stitzel, A. Atala, and J.J. Yoo Cyclic mechanical preconditioning improves engineered muscle contraction Tissue Eng. Part A 14 2008 473 482
185. C. Rhim, D.A. Lowell, M.C. Reedy, D.H. Slentz, S.J. Zhang, W.E. Kraus, and et al. Morphology and ultrastructure of differentiating three-dimensional mammalian skeletal muscle in a collagen gel Muscle Nerve 36 2007 71 80
186. S.J. Bidarra, C.C. Barrias, and P.L. Granja Injectable alginate hydrogels for cell delivery in tissue engineering Acta Biomater. 10 2014 1646 1662
187. B.D. Walters, and J.P. Stegemann Strategies for directing the structure and function of three-dimensional collagen biomaterials across length scales Acta Biomater. 10 2014 1488 1501
188. S. Chattopadhyay, and R.T. Raines Review collagen-based biomaterials for wound healing Biopolymers 101 2014 821 833
189. A.C. Brown, and T.H. Barker Fibrin-based biomaterials: modulation of macroscopic properties through rational design at the molecular level Acta Biomater. 10 2014 1502 1514
190. J.W. Andrejecsk, J. Cui, W.G. Chang, J. Devalliere, J.S. Pober, and W.M. Saltzman Paracrine exchanges of molecular signals between alginate-encapsulated pericytes and freely suspended endothelial cells within a 3D protein gel Biomaterials 34 2013 8899 8908
191. J.A. Rowley, G. Madlambayan, and D.J. Mooney Alginate hydrogels as synthetic extracellular matrix materials Biomaterials 20 1999 45 53
192. T. Boontheekul, H.J. Kong, and D.J. Mooney Controlling alginate gel degradation utilizing partial oxidation and bimodal molecular weight distribution Biomaterials 26 2005 2455 2465
193. J.L. Drury, T. Boontheekul, and D.J. Mooney Cellular cross-linking of peptide modified hydrogels J. Biomech. Eng. 127 2005 220 228
194. L. Wang, J. Shansky, C. Borselli, D. Mooney, and H. Vandenburgh Design and fabrication of a biodegradable, covalently crosslinked shape-memory alginate scaffold for cell and growth factor delivery Tissue Eng. Part A 18 2012 2000 2007
195. T. Boontheekul, E.E. Hill, H.J. Kong, and D.J. Mooney Regulating myoblast phenotype through controlled gel stiffness and degradation Tissue Eng. 13 2007 1431 1442
196. L. Wang, L. Cao, J. Shansky, Z. Wang, D. Mooney, and H. Vandenburgh Minimally invasive approach to the repair of injured skeletal muscle with a shape-memory scaffold Mol. Ther. 22 2014 1441 1449
197. D. Shvartsman, H. Storrie-White, K. Lee, C. Kearney, Y. Brudno, N. Ho, and et al. Sustained delivery of VEGF maintains innervation and promotes reperfusion in ischemic skeletal muscles via NGF/GDNF signaling Mol. Ther. 22 2014 1243 1253
198. M.K. Smith, M.C. Peters, T.P. Richardson, J.C. Garbern, and D.J. Mooney Locally enhanced angiogenesis promotes transplanted cell survival Tissue Eng. 10 2004 63 71
199. C. Borselli, C.A. Cezar, D. Shvartsman, H.H. Vandenburgh, and D.J. Mooney The role of multifunctional delivery scaffold in the ability of cultured myoblasts to promote muscle regeneration Biomaterials 32 2011 8905 8914
200. B. Chevallay, and D. Herbage Collagen-based biomaterials as 3D scaffold for cell cultures: applications for tissue engineering and gene therapy Med. Biol. Eng. Comput. 38 2000 211 218
201. R. Parenteau-Bareil, R. Gauvin, and F. Berthod Collagen-based biomaterials for tissue engineering applications Materials 3 2010 1863 1887
202. S. Carnio, E. Serena, C.A. Rossi, P. De Coppi, N. Elvassore, and L. Vitiello Three-dimensional porous scaffold allows long-term wild-type cell delivery in dystrophic muscle J. Tissue Eng. Regener. Med. 5 2011 1 10
203. E. Serena, M. Flaibani, S. Carnio, L. Boldrin, L. Vitiello, P. De Coppi, and et al. Electrophysiologic stimulation improves myogenic potential of muscle precursor cells grown in a 3D collagen scaffold Neurol. Res. 30 2008 207 214
204. P.B. van Wachem, L.A. Brouwer, and M.J. van Luyn Absence of muscle regeneration after implantation of a collagen matrix seeded with myoblasts Biomaterials 20 1999 419 426
205. S. Kin, A. Hagiwara, Y. Nakase, Y. Kuriu, S. Nakashima, T. Yoshikawa, and et al. Regeneration of skeletal muscle using in situ tissue engineering on an acellular collagen sponge scaffold in a rabbit model ASAIO J. 53 2007 506 513
206. P.B. van Wachem, J.A. Plantinga, M.J. Wissink, R. Beernink, A.A. Poot, G.H. Engbers, and et al. In vivo biocompatibility of carbodiimide-crosslinked collagen matrices: effects of crosslink density, heparin immobilization, and bFGF loading J. Biomed. Mater. Res. 55 2001 368 378
207. J.L. Makridakis, G.D. Pins, T. Dominko, R.L. Page, Design of a novel engineered muscle construct using muscle derived fibroblastic cells seeded onto braided collagen threads, in: Bioengineering Conference, 2009 IEEE 35th Annual Northeast, 2009, pp. 1-2.
208. S.P. Frey, H. Jansen, M.J. Raschke, R.H. Meffert, and S. Ochman VEGF improves skeletal muscle regeneration after acute trauma and reconstruction of the limb in a rabbit model Clin. Orthop. Relat. Res. 470 2012 3607 3614
209. Y.M. Ju, A. Atala, J.J. Yoo, and S.J. Lee In situ regeneration of skeletal muscle tissue through host cell recruitment Acta Biomater. 10 2014 4332 4339
210. R.A. Clark Fibrin and wound healing Ann. NY. Acad. Sci. 936 2001 355 367
211. S. Chiron, C. Tomczak, A. Duperray, J. Laine, G. Bonne, A. Eder, and et al. Complex Interactions between human myoblasts and the surrounding 3D fibrin-based matrix PLoS One 7 2012
212. W. Bian, and N. Bursac Engineered skeletal muscle tissue networks with controllable architecture Biomaterials 30 2009 1401 1412
213. N.R. Martin, S.L. Passey, D.J. Player, A. Khodabukus, R.A. Ferguson, A.P. Sharples, and et al. Factors affecting the structure and maturation of human tissue engineered skeletal muscle Biomaterials 34 2013 5759 5765
214. J.P. Beier, U. Kneser, J. Stern-Strater, G.B. Stark, and A.D. Bach Y chromosome detection of three-dimensional tissue-engineered skeletal muscle constructs in a syngeneic rat animal model Cell Transplant. 13 2004 45 53
215. C. Gerard, M.A. Forest, G. Beauregard, D. Skuk, and J.P. Tremblay Fibrin gel improves the survival of transplanted myoblasts Cell Transplant. 21 2012 127 137
216. D.W. Hammers, A. Sarathy, C.B. Pham, C.T. Drinnan, R.P. Farrar, and L.J. Suggs Controlled release of IGF-I from a biodegradable matrix improves functional recovery of skeletal muscle from ischemia/reperfusion Biotechnol. Bioeng. 109 2012 1051 1059
217. K.G. Cornwell, and G.D. Pins Discrete crosslinked fibrin microthread scaffolds for tissue regeneration J. Biomed. Mater. Res. A 82 2007 104 112
218. K.G. Cornwell, and G.D. Pins Enhanced proliferation and migration of fibroblasts on the surface of fibroblast growth factor-2-loaded fibrin microthreads Tissue Eng. Part A 16 2010 3669 3677
219. J.M. Grasman, L.M. Pumphrey, M. Dunphy, J. Perez-Rogers, and G.D. Pins Static axial stretching enhances the mechanical properties and cellular responses of fibrin microthreads Acta Biomater. 10 2014 4367 4376
220. A.K. McNally, and J.M. Anderson Phenotypic expression in human monocyte-derived interleukin-4-induced foreign body giant cells and macrophages in vitro: dependence on material surface properties J. Biomed. Mater. Res. A 103 2015 1380 1390
221. T. Matsumoto, J. Sasaki, E. Alsberg, H. Egusa, H. Yatani, and T. Sohmura Three-dimensional cell and tissue patterning in a strained fibrin gel system PLoS One 2 2007 e1211
222. I. Stratos, J. Graff, R. Rotter, T. Mittlmeier, and B. Vollmar Open blunt crush injury of different severity determines nature and extent of local tissue regeneration and repair J. Orthop. Res. 28 2010 950 957
223. X. Wu, B.T. Corona, X. Chen, and T.J. Walters A standardized rat model of volumetric muscle loss injury for the development of tissue engineering therapies BioRes. Open Access 1 2012 280 290
224. M. Mirotsou, T.M. Jayawardena, J. Schmeckpeper, M. Gnecchi, and V.J. Dzau Paracrine mechanisms of stem cell reparative and regenerative actions in the heart J. Mol. Cell. Cardiol. 50 2011 280 289