Study of biocompatibility of small intestinal submucosa (SIS) with Schwann cells in vitro

Brain Research

Volumn 1145, Issue 1, 2007, Pages 41-47

  Su, Yan ^a   Zeng, Bing Fang ^a   Zhang, Chang Qing ^a   Zhang, Kai Gang ^a   Xie, Xue Tao ^a  

^a SHANGHAI JIAO TONG UNIVERSITY   (China)

Author keywords

Biocompatibility; Peripheral nerve regeneration; Schwann cell; Small intestinal submucosa

Indexed keywords

3 (4,5 DIMETHYL 2 THIAZOLYL) 2,5 DIPHENYLTETRAZOLIUM BROMIDE; BIOMATERIAL; BRAIN DERIVED NEUROTROPHIC FACTOR; MESSENGER RNA; NERVE GROWTH FACTOR BETA SUBUNIT;

ANIMAL CELL; ARTICLE; AUTOGRAFT; BIOCOMPATIBILITY; CELL ADHESION; CELL MIGRATION; CELL PROLIFERATION; CELL STRUCTURE; CELL VIABILITY; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; IN VITRO STUDY; INTESTINE MUCOSA; MICROSCOPY; NERVE FIBER REGENERATION; NEWBORN; NONHUMAN; PERIPHERAL NERVE INJURY; PRIORITY JOURNAL; PROTEIN SECRETION; QUANTITATIVE ANALYSIS; RAT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SCANNING ELECTRON MICROSCOPY; SCHWANN CELL; SMALL INTESTINE SUBMUCOSA; TISSUE ENGINEERING; TISSUE REPAIR; TRANSMISSION ELECTRON MICROSCOPY;

ANIMALS; ANIMALS, NEWBORN; BIOCOMPATIBLE MATERIALS; BRAIN-DERIVED NEUROTROPHIC FACTOR; CELL ADHESION; CELL MOVEMENT; CELL PROLIFERATION; CELL SURVIVAL; CELLS, CULTURED; GRAFT SURVIVAL; INTESTINAL MUCOSA; INTESTINE, SMALL; MICROSCOPY, ELECTRON, SCANNING; MICROSCOPY, ELECTRON, TRANSMISSION; NERVE GROWTH FACTOR; NERVE REGENERATION; PERIPHERAL NERVES; PERIPHERAL NERVOUS SYSTEM DISEASES; RATS; RATS, SPRAGUE-DAWLEY; RNA, MESSENGER; SCHWANN CELLS; SUS SCROFA; TISSUE ENGINEERING;

RATTUS;

EID: 33947653151     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2007.01.138     Document Type: Article

References (31)

1. Abraham G.A., Murray J., Billiar K., and Sullivan S.J. Evaluation of the porcine intestinal collagen layer as a biomaterial. J. Biomed. Mater. Res. 51 (2000) 442-452
2. Allman A.J., McPherson T.B., Badylak S.F., Merrill L.C., Kallakury B., Sheehan C., Raeder R.H., and Metzger D.W. Xenogeneic extracellular matrix grafts elicit a TH2-restricted immune response. Transplantation 71 (2001) 1631-1640
3. Badylak S.F., Lantz G.C., Coffey A., and Geddes L.A. Small intestinal submucosa as a large diameter vascular graft in the dog. J. Surg. Res. 47 (1989) 74-80
4. Badylak S., Liang A., Record R., Tullius R., and Hodde J. Endothelial cell adherence to small intestinal submucosa: an acellular bioscaffold. Biomaterials 20 (1999) 2257-2263
5. Bellamkonda R.V. Peripheral nerve regeneration: an opinion on channels, scaffolds and anisotropy. Biomaterials 27 (2006) 3515-3518
6. Campodonico F., Benelli R., Michelazzi A., Ognio E., Toncini C., and Maffezzini M. Bladder cell culture on small intestinal submucosa as bioscaffold: experimental study on engineered urothelial grafts. Eur. Urol. 46 (2004) 531-537
7. Evans G.R., Brandt K., Katz S., Chauvin P., Otto L., Bogle M., Wang B., Meszlenyi R.K., Lu L., Mikos A.G., and Patrick Jr. C.W. Bioactive poly(l-lactic acid) conduits seeded with Schwann cells for peripheral nerve regeneration. Biomaterials 23 (2002) 841-848
8. Fansa H., and Keilhoff G. Comparison of different biogenic matrices seeded with cultured Schwann cells for bridging peripheral nerve defects. Neurol. Res. 26 (2004) 167-173
9. Fawcett J.W., and Keynes R.J. Peripheral nerve regeneration. Annu. Rev. Neurosci. 13 (1990) 43-60
10. Greca F.H., Noronha L., Bendhack M., Feres A., Soccol A., and Duda J.R. Use of small intestine submucosa as ureteral allograft in pigs. Int. Braz. J. Urol. 30 (2004) 327-335
11. Hadlock T.A., Sundback C.A., Hunter D.A., Vacanti J.P., and Cheney M.L. A new artificial nerve graft containing rolled Schwann cell monolayers. Microsurgery 21 (2001) 96-101
12. Hudson T.W., Evans G.R., and Schmidt C.E. Engineering strategies for peripheral nerve repair. Clin. Plast. Surg. 26 (1999) 617-628
13. Hurst R.E., and Bonner R.B. Mapping of the distribution of significant proteins and proteoglycans in small intestinal submucosa by fluorescence microscopy. J. Biomater. Sci., Polym. Ed. 12 (2001) 1267-1279
14. Keilhoff G., Stang F., Wolf G., and Fansa H. Bio-compatibility of type I/III collagen matrix for peripheral nerve reconstruction. Biomaterials 24 (2003) 2779-2787
15. Lindberg K., and Badylak S.F. Porcine small intestinal submucosa (SIS): a bioscaffold supporting in vitro primary human epidermal cell differentiation and synthesis of basement membrane proteins. Burn 27 (2001) 254-266
16. Lundborg G. Nerve regeneration: the nerve chamber as an experimental tool. Nerve Injury and Repair (1988), Churchill Libingstone, New York 163-178
17. Lundborg G., and Malmö. A 25-year perspective of peripheral nerve surgery: evolving neuroscientific concepts and clinical significance. J. Hand Surg. 25 (2000) 391-414
18. Machinnon S.E., and Dellon A.L. Clinical nerve reconstruction with a bioabsorbable polyglycolic acid tube. Plast. Reconstr. Surg. 85 (1990) 419-424
19. Mackmmon S.E., and Dellon A.L. Clinical nerve reconstruction with a bioabsorbable polyglycolic acid tube. Plast. Reconstr. Surg. 85 (1990) 419-424
20. Martini R. Expression and functional roles of neural cell surface molecules and extracellular matrix components during development and regeneration of peripheral nerve. J. Neurocytol. 23 (1994) 1-28
21. Mauritz C., Grothe C., and Haastert K. Comparative study of cell culture and purification methods to obtain highly enriched cultures of proliferating adult rat Schwann cells. J. Neurosci. Res. 77 (2004) 453-461
22. Rochkind S., Astachov L., el-Ani D., Hayon T., Graif M., Barsky L., Alon M., Odvak I., Nevo Z., and Shahar A. Further development of reconstructive and cell tissue-engineering technology for treatment of complete peripheral nerve injury in rats. Neurol. Res. 26 (2004) 161-166
23. Schicho R., Skofitsch G., and Donnerer J. Regenerative effect of human recombinant NGF on capsaicin-lesioned sensory neurons in the adult rat. Brain Res. 815 (1999) 60-69
24. Serpe C.J., Byram S.C., Sanders V.M., and Jones K.J. Brain-derived neurotrophic factor supports facial motoneuron survival after facial nerve transection in immunodeficient mice. Brain Behav. Immun. 19 (2005) 173-180
25. Smith R.M., Wiedl C., Chubb P., and Greene C.H. Role of small intestine submucosa (SIS) as a nerve conduit: preliminary report. J. Invest. Surg. 17 (2004) 339-344
26. Suckow M.A., Voytik-Harbin S.L., Terril L.A., and Badylak S.F. Enhanced bone regeneration using porcine small intestinal submucosa. J. Invest. Surg. 12 (1999) 277-287
27. Sulaiman O.A., and Gordon T. Transforming growth factor-beta and forskolin attenuate the adverse effects of long-term Schwann cell denervation on peripheral nerve regeneration in vivo. Glia 37 (2002) 206-218
28. Terzis J.K., Sun D.D., and Thanos P.K. History and basic science review: past, present, and future of nerve repair. J. Reconstr. Microsurg. 13 (1997) 215-225
29. Thompson D.M., and Buettner H.M. Oriented Schwann cell monolayers for directed neurite outgrowth. Ann. Biomed. Eng. 32 (2004) 1120-1130
30. Voytik-Harbin S.L., Brightman A.O., Kraine M.R., Waisner B., and Badylak S.F. Identification of extractable growth factors from small intestinal submucosa. J. Cell. Biochem. 67 (1997) 478-491
31. Zhang F., Zhang J., Lin S., Oswald T., Sones W., Cai Z., Dorsett-Martin W., and Lineaweaver W.C. Small intestinal submucosa in abdominal wall repair after TRAM flap harvesting in a rat model. Plast. Reconstr. Surg. 112 (2003) 565-570