The effect of bioreactor induced vibrational stimulation on extracellular matrix production from human derived fibroblasts

Biomaterials

Volumn 30, Issue 3, 2009, Pages 327-335

  Wolchok, Jeffrey C ^a   Brokopp, Chad ^a   Underwood, Clayton J ^a   Tresco, Patrick A ^a  

^a UNIVERSITY OF UTAH   (United States)

Author keywords

Bioreactor; Collagen; Polyurethane; Vibration; Vocal fold

Indexed keywords

ABS RESINS; ANIMAL CELL CULTURE; BIOLOGICAL MATERIALS; BIOMATERIALS; BIOREACTORS; CELL CULTURE; CHEMICAL REACTORS; COLLAGEN; FIBROBLASTS; GENE EXPRESSION; GENES; INDUSTRIAL CHEMICALS; LATTICE VIBRATIONS; MECHANICAL PROPERTIES; NUCLEIC ACIDS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC SOLVENTS; POLYMERS; PROTEINS; SUBSTRATES; TISSUE;

COLLAGEN TYPE 1; CYCLIC STRAINS; CYTOKINE; CYTOKINE PRODUCTIONS; DNA MICROARRAYS; EXTRACELLULAR MATRIX PRODUCTIONS; EXTRACELLULAR MATRIXES; HIGH FREQUENCIES; HUMAN CELLS; HUMAN SUBJECTS; MATERIAL PROPERTIES; MATRIX DEPOSITIONS; MATRIX PROTEINS; MECHANICAL STIMULUS; POLYMER FOAMS; SEEDED SUBSTRATES; SUBSTRATE VIBRATIONS; THERAPEUTIC APPLICATIONS; VIBRATION; VOCAL FOLD; VOCAL FOLDS;

STIFFNESS MATRIX;

BIOMATERIAL; COLLAGEN; COLLAGEN TYPE 1; COMPLEMENTARY DNA; CYTOKINE; DNA; FIBRONECTIN; MESSENGER RNA; MONOCYTE CHEMOTACTIC PROTEIN 1; POLYURETHAN; TRANSFORMING GROWTH FACTOR BETA1;

ARTICLE; BIOREACTOR; CONTROLLED STUDY; CYTOKINE PRODUCTION; DNA MICROARRAY; ENZYME LINKED IMMUNOSORBENT ASSAY; EXTRACELLULAR MATRIX; GENE EXPRESSION; HUMAN; HUMAN CELL; LARYNX; PHONATION; PRIORITY JOURNAL; PROTEIN SYNTHESIS; VIBRATION; VOCAL CORD;

BIOREACTORS; CHEMOKINE CCL2; CULTURE MEDIA; EXTRACELLULAR MATRIX; FIBROBLASTS; FREEZE DRYING; HUMANS; MECHANICAL PROCESSES; MICROSCOPY, CONFOCAL; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; TISSUE SCAFFOLDS; TRANSFORMING GROWTH FACTOR BETA1; VIBRATION;

EID: 55249096425     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2008.08.035     Document Type: Article

References (45)

1. Baijens L., Speyer R., Linssen M., Ceulen R., and Manni J.J. Rejection of injectable silicone "Bioplastique" used for vocal fold augmentation. Eur Arch Otorhinolaryngol 264 (2007) 565-568
2. Hirano M., Mori K., Tanaka S., and Fujita M. Vocal function in patients with unilateral vocal fold paralysis before and after silicone injection. Acta Otolaryngol 115 (1995) 553-559
3. Ingber D.E. Cellular mechanotransduction: putting all the pieces together again. Faseb J 20 (2006) 811-827
4. Honda K., Ohno S., Tanimoto K., Ijuin C., Tanaka N., Doi T., et al. The effects of high magnitude cyclic tensile load on cartilage matrix metabolism in cultured chondrocytes. Eur J Cell Biol 79 (2000) 601-609
5. Breen E.C. Mechanical strain increases type I collagen expression in pulmonary fibroblasts in vitro. J Appl Phys 88 (2000) 203-209
6. Riser B.L., Cortes P., Yee J., Sharba A.K., Asano K., Rodriguez-Barbero A., et al. Mechanical strain- and high glucose-induced alterations in mesangial cell collagen metabolism: role of TGF-beta. J Am Soc Nephrol 9 (1998) 827-836
7. Gutierrez J.A., and Perr H.A. Mechanical stretch modulates TGF-beta1 and alpha1(I) collagen expression in fetal human intestinal smooth muscle cells. Am J Phys 277 (1999) G1074-G1080
8. Androjna C., Spragg R.K., and Derwin K.A. Mechanical conditioning of cell-seeded small intestine submucosa: a potential tissue-engineering strategy for tendon repair. Tissue Eng 13 (2007) 233-243
9. Jeong S.I., Kwon J.H., Lim J.I., Cho S.W., Jung Y., Sung W.J., et al. Mechano-active tissue engineering of vascular smooth muscle using pulsatile perfusion bioreactors and elastic PLCL scaffolds. Biomaterials 26 (2005) 1405-1411
10. Webb K., Hitchcock R.W., Smeal R.M., Li W., Gray S.D., and Tresco P.A. Cyclic strain increases fibroblast proliferation, matrix accumulation, and elastic modulus of fibroblast-seeded polyurethane constructs. J Biomech 39 (2006) 1136-1144
11. Titze I.R., Hitchcock R.W., Broadhead K., Webb K., Li W., Gray S.D., et al. Design and validation of a bioreactor for engineering vocal fold tissues under combined tensile and vibrational stresses. J Biomech 37 (2004) 1521-1529
12. Sato J.D., and Kan M. Media for culture of mammalian cells. Curr Protoc Cell Biol (2001) [chapter 1: unit 1 2]
13. Fitch J.L., and Holbrook A. Modal fundamental frequency of young adults. Arch Otolaryngol 92 (1970) 379-382
14. Jiang J.J., and Titze I.R. A methodological study of hemilaryngeal phonation. Laryngoscope 103 (1993) 872-882
15. Doellinger M., and Berry D.A. Visualization and quantification of the medial surface dynamics of an excised human vocal fold during phonation. J Voice 20 (2006) 401-413
16. Schuster M., Lohsceller J., Kummer P., Eysholdt U., and Hoppe U. Laser projection in high speed glottography for high precision measurement of laryngeal dimensions and dynamics. Eur Arch Otorhinolaryngol 262 (2005) 477-481
17. Masuda T., Ikeda Y., Manako H., and Komiyama S. Analysis of vocal abuse: fluctuations in phonation time and intensity in 4 groups of speakers. Acta Otolaryngol 113 (1993) 547-552
18. Blatti S.P., Foster D.N., Ranganathan G., Moses H.L., and Getz M.J. Induction of fibronectin gene transcription and mRNA is a primary response to growth-factor stimulation of AKR-2B cells. Proc Natl Acad Sci U S A 85 (1988) 1119-1123
19. Pierce G.F., Mustoe T.A., Altrock B.W., Deuel T.F., and Thomason A. Role of platelet-derived growth factor in wound healing. J Cell Biochem 45 (1991) 319-326
20. Wang J.F., Olson M.E., Ball D.K., Brigstock D.R., and Hart D.A. Recombinant connective tissue growth factor modulates porcine skin fibroblast gene expression. Wound Repair Regen 11 (2003) 220-229
21. Gray S.D., Titze I.R., Alipour F., and Hammond T.H. Biomechanical and histologic observations of vocal fold fibrous proteins. Ann Otol Rhinol Laryngol 109 (2000) 77-85
22. Madruga de Melo E.C., Lemos M., Aragao Ximenes Filho J., Sennes L.U., Nascimento Saldiva P.H., and Tsuji D.H. Distribution of collagen in the lamina propria of the human vocal fold. Laryngoscope 113 (2003) 2187-2191
23. Hirschi S.D., Gray S.D., and Thibeault S.L. Fibronectin: an interesting vocal fold protein. J Voice 16 (2002) 310-316
24. Gokorsch S., Nehring D., Grottke C., and Czermak P. Hydrodynamic stimulation and long term cultivation of nucleus pulposus cells: a new bioreactor system to induce extracellular matrix synthesis by nucleus pulposus cells dependent on intermittent hydrostatic pressure. Int J Artif Organs 27 (2004) 962-970
25. Juncosa-Melvin N., Matlin K.S., Holdcraft R.W., Nirmalanandhan V.S., and Butler D.L. Mechanical stimulation increases collagen type I and collagen type III gene expression of stem cell-collagen sponge constructs for patellar tendon repair. Tissue Eng 13 (2007) 1219-1226
26. Kasra M., Goel V., Martin J., Wang S.T., Choi W., and Buckwalter J. Effect of dynamic hydrostatic pressure on rabbit intervertebral disc cells. J Orthop Res 21 (2003) 597-603
27. Screen H.R., Shelton J.C., Bader D.L., and Lee D.A. Cyclic tensile strain upregulates collagen synthesis in isolated tendon fascicles. Biochem Biophys Res Commun 336 (2005) 424-429
28. Takeuchi R., Saito T., Ishikawa H., Takigami H., Dezawa M., Ide C., et al. Effects of vibration and hyaluronic acid on activation of three-dimensional cultured chondrocytes. Arthritis Rheum 54 (2006) 1897-1905
29. Liu J., Sekiya I., Asai K., Tada T., Kato T., and Matsui N. Biosynthetic response of cultured articular chondrocytes to mechanical vibration. Res Exp Med (Berl) 200 (2001) 183-193
30. Quaglino Jr. D., Nanney L.B., Ditesheim J.A., and Davidson J.M. Transforming growth factor-beta stimulates wound healing and modulates extracellular matrix gene expression in pig skin: incisional wound model. J Invest Dermatol 97 (1991) 34-42
31. Gharaee-Kermani M., Denholm E.M., and Phan S.H. Costimulation of fibroblast collagen and transforming growth factor beta1 gene expression by monocyte chemoattractant protein-1 via specific receptors. J Biol Chem 271 (1996) 17779-17784
32. Eskin S.G., Ives C.L., McIntire L.V., and Navarro L.T. Response of cultured endothelial cells to steady flow. Microvasc Res 28 (1984) 87-94
33. Li S., Kim M., Hu Y.L., Jalali S., Schlaepfer D.D., Hunter T., et al. Fluid shear stress activation of focal adhesion kinase. Linking to mitogen-activated protein kinases. J Biol Chem 272 (1997) 30455-30462
34. Dieterich P., Odenthal-Schnittler M., Mrowietz C., Kramer M., Sasse L., Oberleithner H., et al. Quantitative morphodynamics of endothelial cells within confluent cultures in response to fluid shear stress. Biophys J 79 (2000) 1285-1297
35. Magid R., Murphy T.J., and Galis Z.S. Expression of matrix metalloproteinase-9 in endothelial cells is differentially regulated by shear stress. Role of c-Myc. J Biol Chem 278 (2003) 32994-32999
36. Davies P.F. Flow-mediated endothelial mechanotransduction. Physiol Rev 75 (1995) 519-560
37. Wang Y., Botvinick E.L., Zhao Y., Berns M.W., Usami S., Tsien R.Y., et al. Visualizing the mechanical activation of Src. Nature 434 (2005) 1040-1045
38. Li S., Butler P., Wang Y., Hu Y., Han D.C., Usami S., et al. The role of the dynamics of focal adhesion kinase in the mechanotaxis of endothelial cells. Proc Natl Acad Sci U S A 99 (2002) 3546-3551
39. Urbich C., Walter D.H., Zeiher A.M., and Dimmeler S. Laminar shear stress upregulates integrin expression: role in endothelial cell adhesion and apoptosis. Circ Res 87 (2000) 683-689
40. Shyy J.Y., and Chien S. Role of integrins in endothelial mechanosensing of shear stress. Circ Res 91 (2002) 769-775
41. Gloe T., Sohn H.Y., Meininger G.A., and Pohl U. Shear stress-induced release of basic fibroblast growth factor from endothelial cells is mediated by matrix interaction via integrin alpha(v)beta3. J Biol Chem 277 (2002) 23453-23458
42. Maniotis A.J., Chen C.S., and Ingber D.E. Demonstration of mechanical connections between integrins, cytoskeletal filaments, and nucleoplasm that stabilize nuclear structure. Proc Natl Acad Sci U S A 94 (1997) 849-854
43. Katsumi A., Orr A.W., Tzima E., and Schwartz M.A. Integrins in mechanotransduction. J Biol Chem 279 (2004) 12001-12004
44. Malone A.M., Anderson C.T., Tummala P., Kwon R.Y., Johnston T.R., Stearns T., et al. Primary cilia mediate mechanosensing in bone cells by a calcium-independent mechanism. Proc Natl Acad Sci U S A 104 (2007) 13325-13330
45. Juncosa-Melvin N., Shearn J.T., Boivin G.P., Gooch C., Galloway M.T., West J.R., et al. Effects of mechanical stimulation on the biomechanics and histology of stem cell-collagen sponge constructs for rabbit patellar tendon repair. Tissue Eng 12 (2006) 2291-2300