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1.
Microsurgery ; 20(3): 126-30, 2000.
Article in English | MEDLINE | ID: mdl-10790175

ABSTRACT

We have found previously that expansion of the Wallerian degenerated nerve was accompanied by accelerated Schwann cell proliferation. In this study, we investigated the usefulness of the elongation of Wallerian degenerated nerve for the repair of short nerve gap. Male Wistar rats were used. After the left sciatic nerve was transected the rats were divided into 4 groups. In the control group, nerve coaptation was not performed. In group 1, tensionless coaptation was performed immediately. In group 2, delayed tensionless coaptation was performed with the elongation of Wallerian degenerated nerve. In group 3, coaptation was performed immediately with autologous interposition nerve graft. The ideal tensionless nerve repair of group 1 was considered to produce the best result. Rats in group 2 showed functional recovery as good as rats in group 1. On histologic assessment, in group 2, a fibrous capsule that was very rich in vascularity was formed around the tissue expander. After 14 weeks, the capsule was diminished markedly in size, but the vascularity was rich around the sciatic nerve. We think that the excellent functional recovery seen in group 2 can be attributed to the increased activity of Schwann cell proliferation and increased vascularity.


Subject(s)
Tissue Expansion , Wallerian Degeneration/surgery , Animals , Axons/physiology , Cell Division , Male , Microsurgery , Rats , Rats, Wistar , Schwann Cells/physiology , Sciatic Nerve/surgery , Wallerian Degeneration/pathology
2.
J Orthop Sci ; 4(1): 22-7, 1999.
Article in English | MEDLINE | ID: mdl-9914425

ABSTRACT

We investigated the expression of tyrosine kinase receptors (trkBs) and their ligand, brain-derived neurotrophic factor (BDNF), in isolated sciatic nerve segments of rat in a silicone chamber model devoid of axonal contact, using an immunohistochemical technique. The receptor gp 95trkB was not detected during the first 3 weeks but was strongly expressed in the nerve stumps on day 21. In contrast, gp 145trkB immunoreactivity was readily detected in the Schwann cells in the nerve stumps between days 1 and 7 after isolation. Immunohistochemical analysis using anti-S-100 antibody demonstrated that Schwann cell tube formation within the silicone chamber had been completed by the third week, which suggested that gp 95trkB began to be produced by Schwann cells after completion of Schwann cell tube formation. Considering the low level of BDNF production during the first week, molecules other than BDNF may be ligands for gp 145trkB in the silicone chamber model devoid of axonal contact.


Subject(s)
Receptor Protein-Tyrosine Kinases/biosynthesis , Receptors, Nerve Growth Factor/biosynthesis , Schwann Cells/metabolism , Sciatic Nerve/metabolism , Animals , Brain-Derived Neurotrophic Factor/biosynthesis , Follow-Up Studies , Immunoenzyme Techniques , Male , Nerve Regeneration , Rats , Rats, Wistar , Receptor, trkB , S100 Proteins/biosynthesis , Sciatic Nerve/cytology , Sciatic Nerve/injuries , Silicone Elastomers
3.
Apoptosis ; 3(5): 353-60, 1998 Oct.
Article in English | MEDLINE | ID: mdl-14646482

ABSTRACT

The Schwann cell cables provide particularly favorable sites for the growth of regenerating axonal sprouts. However, if they remain denervated, endoneurial fibrosis takes place with the Schwann cells atrophying and total Schwann cell number gradually decrease with time. Even when regenerating axonal sprouts invade into the cables, Schwann cells do not survive for long periods if they fail to make axonal contact. These observations strongly suggest the involvement of apoptosis in peripheral nerve degeneration and regeneration. So, we investigated the behavior of Schwann cells prepared from wallerian-degenerated adult rat sciatic nerve in vitro. The secondary cultured Schwann cells showed serial changes in morphology, mitotic activity and migratory activity as they do during Schwann cell cable formation in vivo. At the final stage of differentiation, the Schwann cells became rounded and detached from the flask with extensive blebbing. Electron micrographs clearly demonstrated typical cytoplasmic changes of apoptosis, but, nuclei of most of the cells retained their size and morphology with residual nucleolar structures. An agarose gel electrophoresis of DNA clearly demonstrated that there was not any DNA fragmentation up to 120 h after detachment. Results by in situ apoptosis detection assay did not show any DNA degradation despite the substantial decrease in Schwann cell number. In conclusion, during peripheral nerve degeneration and regeneration, supernumerary Schwann cells are removed by apoptosis, however, it lacks most of the nuclear events of usual apoptosis.

4.
Muscle Nerve ; 20(10): 1314-7, 1997 Oct.
Article in English | MEDLINE | ID: mdl-9324090

ABSTRACT

We studied the effect of initiation time of nerve expansion after nerve transection on the induction of ODC activity and Schwann cell proliferation in nerve tissue under Wallerian degeneration. The levels of ODC activity and Schwann cell proliferation decreased as the initiation time of nerve expansion was delayed after nerve transection, and peak levels of ODC activity following nerve expansion preceded peak levels of Schwann cell proliferation.


Subject(s)
Nerve Regeneration/physiology , Nerve Tissue/physiopathology , Ornithine Decarboxylase/metabolism , Schwann Cells/cytology , Animals , Cell Division , Denervation , Enzyme Induction , Male , Rats , Rats, Wistar , Time Factors , Wallerian Degeneration/physiology
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