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The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration
Using mAbs and immunocytochemistry we have examined the response of macrophages (M phi) after crush injury to the sciatic or optic nerve in the mouse and rat. We have established that large numbers of M phi enter peripheral nerves containing degenerating axons; the M phi are localized to the portion...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1987
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188570/ https://www.ncbi.nlm.nih.gov/pubmed/3559478 |
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collection | PubMed |
description | Using mAbs and immunocytochemistry we have examined the response of macrophages (M phi) after crush injury to the sciatic or optic nerve in the mouse and rat. We have established that large numbers of M phi enter peripheral nerves containing degenerating axons; the M phi are localized to the portion containing damaged axons, and they phagocytose myelin. The period of recruitment of the M phi in the peripheral nerve is before and during the period of maximal proliferation of the Schwann cells. In contrast, the degenerating optic nerve attracts few M phi, and the removal of myelin is much slower. These results show the clearly different responses of M phi to damage in the central and peripheral nervous systems, and suggest that M phi may be an important component of subsequent repair as well as myelin degradation. |
format | Text |
id | pubmed-2188570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1987 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21885702008-04-17 The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration J Exp Med Articles Using mAbs and immunocytochemistry we have examined the response of macrophages (M phi) after crush injury to the sciatic or optic nerve in the mouse and rat. We have established that large numbers of M phi enter peripheral nerves containing degenerating axons; the M phi are localized to the portion containing damaged axons, and they phagocytose myelin. The period of recruitment of the M phi in the peripheral nerve is before and during the period of maximal proliferation of the Schwann cells. In contrast, the degenerating optic nerve attracts few M phi, and the removal of myelin is much slower. These results show the clearly different responses of M phi to damage in the central and peripheral nervous systems, and suggest that M phi may be an important component of subsequent repair as well as myelin degradation. The Rockefeller University Press 1987-04-01 /pmc/articles/PMC2188570/ /pubmed/3559478 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration |
title | The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration |
title_full | The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration |
title_fullStr | The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration |
title_full_unstemmed | The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration |
title_short | The macrophage response to central and peripheral nerve injury. A possible role for macrophages in regeneration |
title_sort | macrophage response to central and peripheral nerve injury. a possible role for macrophages in regeneration |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2188570/ https://www.ncbi.nlm.nih.gov/pubmed/3559478 |