The use of keratin biomaterials derived from human hair for the promotion of rapid regeneration of peripheral nerves

Biomaterials

Volumn 29, Issue 1, 2008, Pages 118-128

  Sierpinski, Paulina ^a   Garrett, Jeffrey ^a   Ma, Jianjun ^a   Apel, Peter ^a   Klorig, David ^a   Smith, Thomas ^a   Koman, L Andrew ^a   Atala, Anthony ^a   Van Dyke, Mark ^a  

^a WAKE FOREST SCHOOL OF MEDICINE   (United States)

Author keywords

ECM; Keratin; Nerve guide; Nerve regeneration; Schwann cell

Indexed keywords

ANIMALS; CELLS; GENES; NEURONS;

HUMAN HAIR; KERATIN; NEUROINDUCTIVE; PERIPHERAL NERVES; RAPID REGENERATION; SCHWANN CELLS; TRAUMA-ASSOCIATED NERVE DEFECTS; TUBULAR CONDUIT;

BIOMATERIALS;

BIOMATERIAL; KERATIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL ACTIVATION; CELL ADHESION; CELL PROLIFERATION; CHEMOTAXIS; CONTROLLED STUDY; DISEASE MODEL; GEL; GENE EXPRESSION; HAIR; IN VITRO STUDY; INTERMETHOD COMPARISON; MALE; MOLECULAR DYNAMICS; NERVE FUNCTION; NERVE GRAFT; NERVE REGENERATION; NONHUMAN; PERIPHERAL NERVE INJURY; PRIORITY JOURNAL; PROTEIN ISOLATION; RAT; SCHWANN CELL; UPREGULATION;

ANIMALS; BIOCOMPATIBLE MATERIALS; CELL LINE; ELECTROPHYSIOLOGY; GENE EXPRESSION REGULATION; HAIR; HUMANS; HYDROGELS; KERATINS; MALE; NERVE REGENERATION; PERIPHERAL NERVES; POROSITY; RATS; TIME FACTORS;

ANIMALIA;

EID: 35348929350     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2007.08.023     Document Type: Article

References (39)

1. Belkas J.S., Shoichet M.S., and Midha R. Peripheral nerve regeneration through guidance tubes. Neurol Res 26 2 (2004) 151-160
2. Alonso L., and Fuchs E. The hair cycle. J Cell Sci 119 3 (2006) 391-393
3. Stenn K.S., Prouty S.M., and Seiberg M. Molecules of the cycling hair follicle-a tabulated review. J Dermatol Sci 7 Suppl (1994) S109-S124
4. Stenn K.S., Combates N.J., Eilertsen K.J., Gordon J.S., Pardinas J.R., Parimoo S., et al. Hair follicle growth controls. Dermatol Clin 14 4 (1996) 543-548
5. Hardy M.H. The secret life of the hair follicle. Trends Genet 8 2 (1992) 55-61
6. Rogers G.E. Hair follicle differentiation and regulation. Int J Dev Biol 48 2-3 (2004) 163-170
7. Ioannidou E. Therapeutic modulation of growth factors and cytokines in regenerative medicine. Curr Pharm Des 12 19 (2006) 2397-2408
8. Verge V.M., Gratto K.A., Karchewski L.A., and Richardson P.M. Neurotrophins and nerve injury in the adult. Phil Trans R Soc London B Biol Sci 351 1338 (1996) 423-430
9. Frostick S.P., Yin Q., and Kemp G.J. Schwann cells, neurotrophic factors and peripheral nerve regeneration. Microsurgery 18 7 (1998) 397-405
10. Crewther W.G., Fraser R.D.B., Lennox F.G., and Lindley H. The chemistry of keratins. In: Anfinsen Jr. C.B., Anson M.L., Edsall J.T., and Richards F.M. (Eds). Advances in protein chemistry (1965), Academic Press, New York 191-346
11. Noishiki Y., Ito H., Miyamoto T., and Inagaki H. Application of denatured wool keratin derivatives to an antithrombogenic biomaterial: vascular graft coated with a heparinized keratin derivative. Kobunshi Ronbunshu 39 4 (1982) 221-227
12. Katoh K., Tanabe T., and Yamauchi K. Novel approach to fabricate keratin sponge scaffolds with controlled pore size & porosity. Biomaterials 25 18 (2004) 4255-4262
13. Tachibana A., Furuta Y., Takeshima H., Tanabe T., and Yamauchi K. Fabrication of wool keratin sponge scaffolds for long-term cell cultivation. J Biotechnol 93 (2002) 165-170
14. Tachibana A., Kaneko S., Tanabe T., and Yamauchi K. Rapid fabrication of keratin-hydroxyapatite hybrid sponges toward osteoblast cultivation and differentiation. Biomaterials 26 3 (2005) 297-302
15. Bansal R., and Pfeiffer S.E. Regulated galactolipid synthesis and cell surface expression in Schwann cell line D6P2T. J. Neurochem 49 6 (1987) 1902-1911
16. Mosmann T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J Immunol Meth 65 1-2 (1983) 55-63
17. T method. Methods 25 4 (2001) 402-408
18. Thomas H., Conrads A., Phan K.H., van de Löcht M., and Zahn H. In vitro reconstitution of wool intermediate filaments. Int J Biol Macromol 8 (1986) 258-264
19. van de Löcht M. Reconstitution of microfibrils from wool & filaments from epidermis proteins. Melli Textil 10 (1987) 780-786
20. Cory A.H., Owen T.C., Barltrop J.A., and Cory J.G. Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture. Cancer Commun 3 7 (1991) 207-212
21. Hai M., Muja N., DeVries G.H., Quarles R.H., and Patel P.I. Comparative analysis of Schwann cell lines as model systems for myelin gene transcription studies. J Neurosci Res 69 4 (2002) 497-508
22. Boyden S. The chemotactic effect of mixtures of antibody and antigen on polymorphonuclear leucocytes. J Exp Med 115 (1962) 453-466
23. Ingber D. Integrins as mechanochemical transducers. Curr Opin Cell Biol 3 5 (1991) 841-848
24. Tooney P.A., Agrez M.V., and Burns G.F. A re-examination of the molecular basis of cell movement. Immunol Cell Biol 71 2 (1993) 131-139
25. Jockusch B.M., et al. The molecular architecture of focal adhesions. Annu Rev Cell Dev Biol 11 (1995) 379-416
26. Ruoslahti E. RGD and other recognition sequences for integrins. Annu Rev Cell Dev Biol 12 (1996) 697-715
27. Entrez Protein Database. National Center for Biotechnology Information (NCBI). 〈http://www.ncbi.nlm.nih.gov〉.
28. Xiong Z., O'Hanlon D., Becker L.E., Roder J., MacDonald J.F., and Marks A. Enhanced calcium transients in glial cells in neonatal cerebellar cultures derived from S100B null mice. Exp Cell Res 257 2 (2000) 281-289
29. Triolo D., Dina G., Lorenzetti I., Malaguti M., Morana P., Del Carro U., et al. Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferation and delays nerve regeneration after damage. J Cell Sci 119 19 (2006) 3981-3993
30. Anton E.S., Weskamp G., Reichardt L.F., and Matthew W.D. Nerve growth factor and its low-affinity receptor promote Schwann cell migration. Proc Natl Acad Sci USA 91 7 (1994) 2795-2799
31. Ide C. Peripheral nerve regeneration. Neurosci Res 25 2 (1996) 101-121
32. Fu S.Y., and Gordon T. The cellular and molecular basis of peripheral nerve regeneration. Mol Neurobiol 14 1-2 (1997) 67-116
33. Feltri M.L., Scherer S.S., Nemni R., Kamholz J., Vogelbacker H., Scott M.O., et al. Beta 4 integrin expression in myelinating Schwann cells is polarized, developmentally regulated and axonally dependent. Development 120 5 (1994) 1287-1301
34. Sondell M., Lundborg G., and Kanje M. Vascular endothelial growth factor stimulates Schwann cell invasion and neovascularization of acellular nerve grafts. Brain Res 846 2 (1999) 219-228
35. Jones C.M., Lyons K.M., and Hogan B.L.M. Involvement of bone morphogenetic protein-4 (BMP-4) and Vgr-1 in morphogenesis and neurogenesis in the mouse. Development 111 (1991) 531-542
36. Lyons K.M., Pelton R.W., and Hogan B.L.M. Organogenesis and pattern formation in the mouse: RNA distribution patterns suggest a role for bone morphogenetic protein-2A (BMP-2A). Development 109 (1990) 833-844
37. Blessings M., Nanney L.B., King L.E., Jones C.M., and Hogan B.L.M. Transgenic mice as a model to study the role of TGF-ß related molecules in hair follicles. Genes Dev 7 (1993) 204-215
38. Liu H.M. The role of extracellular matrix in peripheral nerve regeneration: a wound chamber study. Acta Neuropathol (Berlin) 83 5 (1992) 469-474
39. Ma J, Shen J, Garrett JP, Lee CA, Li Z, Elsaidi GA et al. Gene expression of myogenic regulatory factors, nicotinic acetylcholine receptor subunits, and GAP-43 in skeletal muscle following denervation in a rat model. J Orthop Res 2007, in press.