Influence of glial growth factor and Schwann cells in a bioresorbable guidance channel on peripheral nerve regeneration

Tissue Engineering

Volumn 6, Issue 2, 2000, Pages 129-138

  Bryan, David J ^a,c   Holway, Antonia H ^a   Wang, Kai Kai ^a   Silva, Alyson E ^b   Trantolo, Debra J ^b   Wise, Donald ^b   Summerhayes, Ian C ^a  

^a LAHEY HOSPITAL AND MEDICAL CENTER   (United States)

^b Cambridge Scientific Inc   (United States)

^c Director of Tissue Engineering   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

NEURITE PROMOTING FACTOR; POLYGLYCOLIC ACID; POLYLACTIC ACID;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIOMEDICAL ENGINEERING; CELL COUNT; CONTROLLED STUDY; FEMALE; HISTOPATHOLOGY; MYELINATION; NERVE FIBER REGENERATION; NONHUMAN; PERIPHERAL NERVE INJURY; PRIORITY JOURNAL; RAT; SCHWANN CELL; SCIATIC NERVE; TREATMENT OUTCOME; VASCULARIZATION;

ANIMALS; AXONS; BIOCOMPATIBLE MATERIALS; BIOMEDICAL ENGINEERING; ELECTROPHYSIOLOGY; FEMALE; LACTIC ACID; MYELIN SHEATH; NEOVASCULARIZATION, PHYSIOLOGIC; NERVE REGENERATION; NEUREGULIN-1; PERIPHERAL NERVES; POLYGLYCOLIC ACID; POLYMERS; RATS; RATS, SPRAGUE-DAWLEY; SCHWANN CELLS;

EID: 0034004945     PISSN: 10763279     EISSN: None     Source Type: Journal    
DOI: 10.1089/107632700320757     Document Type: Article

References (35)

1. Bryan, D.J. Wang, K.-K., and Chakalis-Haley, D. Effect of Schwann cells in the enhancement of peripheral nerve regeneration. J. Reconstr. Microsurg. 12, 439, 1996.
2. Stoll, G., Griffin, J.W., Li, C.Y., and Trapp, B.D. Wallerian degeneration in the peripheral nervous system: Participation of both Schwann cells and macrophages in myelin degeneration. J. Neurocytol. 18, 671, 1989.
3. Guenard, V., Dinarello, C.A., Weston, P.J., and Aebisher, P. Peripheral nerve regeneration is impeded by interleukin-1 receptor antagonist released from polymeric guidance channel. J. Neurosci. Res. 29, 396, 1991.
4. Eccleston, P.A. Regulation of Schwann cell proliferation: Mechanisms involved in peripheral nerve development. Exp. Cell Res. 1, 199, 1992.
5. Morrissey, T.K., Kleitman, N., and Bunge, R.P. Isolation and functional characterization of Schwann cells derived from adult peripheral nerve. J. Neurosci. 11, 2433, 1991.
6. Guenard, V., Aebischer, P., and Bunge, R.P. The astrocyte inhibition of peripheral nerve regeneration is reversed by Schwann cells. Exp. Neurol. 126, 44, 1994.
7. Thanos, P.K., Okajima, S., and Terzis, J.K. Ultrastructure and cellular biology of nerve regeneration. J. Reconstr. Microsurg. 14, 423, 1998.
8. Letourneau, P.C. Cell-to-substratum adhesion and guidance of axonal elongation. Dev. Biol. 44, 92, 1975.
9. Bunge, M.B., Bunge, R.P., Kleitman, N., and Dean, A.C. Role of peripheral nerve extracellular matrix in Schwann cell function and in neurite regeneration. Dev. Neurosci. 11, 348, 1989.
10. Rivas, R.J., Burmeister, D.W., and Goldberg, D.J. Rapid effects of laminin on the growth cone. Neuron 8, 107, 1992.
11. Ide, C., Tohyama, K., Yokota, et al. Schwann cell basal lamina, in rat sciatic nerve regeneration with antiserum treated nerve grafts. Brain Res. 570, 116, 1992.
12. Wang, G.Y., Hirai, K., and Shimada, H. The role of laminin, a component of Schwann cell basal lamina, in a rat sciatic nerve regeneration within antiserum-treated nerve grafts. Brain Res. 570, 116, 1992.
13. Hagg, T., Gulati, A.K., Behzadiam, A., et al. Nerve growth factor promotes CNS cholinergic axonal regeneration into acellular peripheral nerve graft. Exp. Neurol. 112, 79, 1991.
14. Nakao, Y. An experimental study of the effect of laminin in vivo on promoting regeneration in axons. J. Jpn. Orthop. Assoc. 66, 334, 1992.
15. Osawa, T., Tohyama, K., and Ide, C. Allogenic nerve grafts in the rat, with special reference to the role of Schwann cell basal lamina in nerve regeneration. J. Neurocytol. 19, 833, 1990.
16. Minghetti, L., Goodearl, A.D., Mistry, K., and Stroobant, P. Glial growth factors I-III are specific mitogens for glial cells. J. Neurosci. Res. 43, 684, 1996.
17. Marchionni, M.A., Goodearl, A.D., Chen, M.S., et al. Glial growth factors are alternatively spliced erbB2 ligands expressed in the nervous system. Nature 362, 312, 1993.
18. Goodearl, A.D., Davis, J.B., Mistry, K., et al. Purification of multiple forms of glial growth factor. J. Biol. Chem. 268, 18095, 1993.
19. Salzer, J.L., and Bunge, R.P. Studies of Schwann cell proliferation. I. An analysis in tissue culture of proliferation during development, Wallerian degeneration and direct injury. J. Cell Biol. 84, 739, 1980.
20. 3 H)-Thymidine incorporation through their respective receptors. Glia 18, 68, 1996.
21. Carroll, S.L., Miller, M.L., Frohnert, P.W., et al. Expression of neuregulins and their putative receptors, erbB2 and erbB3 induced during Wallerian degeneration. Soc. Neurosci. 22, 1423, 1996.
22. Suzuki, S., Sano, K., and Tanihara, H. Diversity of the cadherin family: Evidence for eight new cadherins in nervous tissue. Cell Regul. 2, 261, 1991.
23. Letourneau, P.C., Shattuck, T.A., Roche, F.K., et al. Nerve growth cone migration onto Schwann Cells involves the calcium-dependent adhesion molecule. Dev. Biol. 138, 430, 1990.
24. Shibuya, Y., Mizoguchi, A., Takeichi, M., et al. Localization of N-cadherin in the normal and regenerating nerve fibers of the chicken peripheral nervous system. Neuroscience 67, 253, 1995.
25. Ignatis, M.J., Large, T.H., Houle, M., et al. Molecular change of the rat integrin α1 subunit: A receptor for laminin and collagen. J. Cell Biol. 111, 709, 1990.
26. Einheber, S., Milner, T.A., Giamocotti, F., and Salzer, J.L. Axonal regulation of Schwann cell integrin expression suggests a role for α6B4 in myelination. J. Cell Biol. 123, 1223, 1993.
27. Taskinen, H.S., Heino, J., and Roytta, M. The dynamics of β1 integrin expression during peripheral nerve regeneration. Acta Neuropathol. 89, 144, 1995.
28. Bixby, J.L., and Jhabvala, P. Extracellular matrix molecules and cell adhesion molecules induce neurites through different mechanisms. J. Cell Biol. 111, 2725, 1995.
29. Araki, T., and Milbrandt, J. Ninjurin, a novel adhesion molecule is induced by nerve injury and promotes axonal growth. Neuron 17, 353, 1996.
30. Hsu, Y.Y., Gresser, J.D., Trantola, D.J., Lyons, C.M., Gangadharam, P.R.J., and Wise, D.L. Effect of polymer foam morphology and density on the kinetics of in vitro controlled release of isoniazid from compressed foam matrices. J. Biomed, Mater. Res. 35, 117, 1997.
31. Bain, J.R., Mackinnon, S.E., and Hunter, D.A. Functional evaluation of complete sciatic, peroneal, and posterior tibial nerve lesions in the rat. Plast. Reconstr. Surg. 1, 129, 1989.
32. Seckel, B.R., Jones, D., Hekimian, K.J., Wang, K.K., Chakalis, D.P., and Costas, P.D. Hyaluronic acid through a new injectable nerve guide delivery system enhances peripheral nerve regeneration in the rat. J. Neuroscience Res. 40, 318, 1995.
33. Den Dunnen, W.F.A., Van Der Lei, B., Schakenraad, J.M., et al. Long-term evaluation of nerve guide regeneration in a biodegradable nerve guide. Microsurgery 14, 508, 1993.
34. Den Dunnen, W.F.A., Van Der Lei, B., Robinson, P.H., et al. Biological performance of a degradable poly(lactic acid-∈-caprolactone) nerve guide: Influence of tube dimensions. J. Biomedical Materials Res. 29, 757, 1995.
35. Thi, A.D., Evrard, C., and Rouget, P. Proliferation and differentiation properties of permanent Schwann cell lines immortalized with a temperature-sensitive oncogene. J. Exp. Biol. 201, 851, 1998.