1994
DOI: 10.1016/0006-8993(94)90492-8
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Axonal reinnervation does not influence Schwann cell proliferation after rat sciatic nerve transection

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Cited by 48 publications
(33 citation statements)
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“…Previous reports have shown that the rate of proliferation of Schwann cells and the appearance of Schwann cell migratory promoting activity in extracellular fluid were increased considerably at 7 Â14 days after transection, and returned to the control level later [17,18]. Our study has shown that the number of proliferating Schwann cells increased significantly in a lengthened nerve at day 20.…”
Section: Discussionsupporting
confidence: 52%
“…Previous reports have shown that the rate of proliferation of Schwann cells and the appearance of Schwann cell migratory promoting activity in extracellular fluid were increased considerably at 7 Â14 days after transection, and returned to the control level later [17,18]. Our study has shown that the number of proliferating Schwann cells increased significantly in a lengthened nerve at day 20.…”
Section: Discussionsupporting
confidence: 52%
“…The production of NDF could be the result of axonal contact which initiates numerous responses in the SC (Neuberger and DeVries, 1992), and the NDF in SC could possibly function after injury to produce a mitotic or differentiation response in SC. Recent evidence suggests that the re-establishment of axonal contact after nerve injury does not elicit SC mitosis (Siironen et al, 1994). Our laboratory has implicated a myelin basic protein as a potential mitogen for SC after neural injury (Baichwal and DeVries, 1992;Tzeng et al, 1995).…”
Section: Functions Of Neuregulins In Scmentioning
confidence: 98%
“…Injuries to peripheral nerves often result in axonal degeneration and removal of their surrounding myelin sheaths by hematogenous, ED11 (immunoreactive) macrophages (Bruck, 1997;Perry et al, 1987), proliferation of Schwann cells (Siironen et al, 1994), increased expression of collagen RNAs (Siironen et al, 1994(Siironen et al, , 1996, and eventually, perineurial and epineurial thickening as a result of increased deposition of collagen and other extracellular matrix components (Siironen et al, 1992(Siironen et al, , 1996. Many of the signals driving these processes remain unknown.…”
Section: Introductionmentioning
confidence: 96%