TY - JOUR
T1 - Peripheral nerve regeneration through alginate gel
T2 - Analysis of early outgrowth and late increase in diameter of regenerating axons
AU - Hashimoto, T.
AU - Suzuki, Y.
AU - Kitada, M.
AU - Kataoka, K.
AU - Wu, S.
AU - Suzuki, K.
AU - Endo, K.
AU - Nishimura, Y.
AU - Ide, C.
N1 - Funding Information:
Acknowledgements This work was supported by a grant from the Japanese Society for Promotion of Science (JSPS-RFTF 96100203 and University-Industry Research Cooperation with Matching Fund) and grants-in-aid 11307037, 11877240, 12771065, 12877285 and 2032753 for scientific research from the Japanese Ministry of Science, Education and Culture.
PY - 2002
Y1 - 2002
N2 - Our previous study revealed that alginate gel cross-linked with covalent bonds promoted peripheral nerve regeneration in the cat and rat. The present study analyzed nerve regeneration through alginate gel in the early stages within 2 weeks and the late stages up to 21 months after implantation. Four days after surgery, regenerating axons grew without Schwann cell investment through the partially degraded alginate gel, being in direct contact with the alginate without a basal lamina covering. Numerous mast cells infiltrated into the alginate. One to 2 weeks after surgery, regenerating axons were surrounded by common Schwann cells to form small bundles, with some axons at the periphery being partly in direct contact with alginate. At the distal stump, numerous Schwann cells had migrated into the alginate 8-14 days after surgery. They had no basal laminae. The diameter of regenerated myelinated fibers was small (approximately 1 μm) at 8 weeks, but increased in diameter, having a distribution pattern similar to that of normal nerve 21 months after surgery. Much better nerve regeneration was found in alginate gel-, than collagen sponge-, and fibrin glue-implanted distal stump 12 months after surgery. These results indicate that alginate gel has good biocompatibility for regenerating axon outgrowth and Schwann cell migration, and that regenerated fibers can have a diameter as thick as that of normal fibers in the long term. Alginate gel is a promising material for use as an implant for peripheral nerve regeneration.
AB - Our previous study revealed that alginate gel cross-linked with covalent bonds promoted peripheral nerve regeneration in the cat and rat. The present study analyzed nerve regeneration through alginate gel in the early stages within 2 weeks and the late stages up to 21 months after implantation. Four days after surgery, regenerating axons grew without Schwann cell investment through the partially degraded alginate gel, being in direct contact with the alginate without a basal lamina covering. Numerous mast cells infiltrated into the alginate. One to 2 weeks after surgery, regenerating axons were surrounded by common Schwann cells to form small bundles, with some axons at the periphery being partly in direct contact with alginate. At the distal stump, numerous Schwann cells had migrated into the alginate 8-14 days after surgery. They had no basal laminae. The diameter of regenerated myelinated fibers was small (approximately 1 μm) at 8 weeks, but increased in diameter, having a distribution pattern similar to that of normal nerve 21 months after surgery. Much better nerve regeneration was found in alginate gel-, than collagen sponge-, and fibrin glue-implanted distal stump 12 months after surgery. These results indicate that alginate gel has good biocompatibility for regenerating axon outgrowth and Schwann cell migration, and that regenerated fibers can have a diameter as thick as that of normal fibers in the long term. Alginate gel is a promising material for use as an implant for peripheral nerve regeneration.
KW - Alginate gel
KW - Axonal outgrowth
KW - Electron microscopy
KW - Electrophysiology
KW - Immunohistochemistry
KW - Peripheral nerve regeneration
KW - Schwann cell basal lamina
KW - Schwann cell migration
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U2 - 10.1007/s00221-002-1173-y
DO - 10.1007/s00221-002-1173-y
M3 - Article
C2 - 12232692
AN - SCOPUS:0036381976
SN - 0014-4819
VL - 146
SP - 356
EP - 368
JO - Experimental Brain Research
JF - Experimental Brain Research
IS - 3
ER -