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PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division

Primary cultures of rat dorsal root ganglion Schwann cells were used to assay the efficacy of PC12 cells in stimulating Schwann cell proliferation. Co-cultures of PC12 cells and Schwann cells assayed by [3H]thymidine labeling followed by autoradiography showed proliferation of Schwann cells only whe...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1984
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113132/
https://www.ncbi.nlm.nih.gov/pubmed/6321518
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description Primary cultures of rat dorsal root ganglion Schwann cells were used to assay the efficacy of PC12 cells in stimulating Schwann cell proliferation. Co-cultures of PC12 cells and Schwann cells assayed by [3H]thymidine labeling followed by autoradiography showed proliferation of Schwann cells only where contact occurred between PC12 neurites and Schwann cells. Membranes derived from PC12 cells were shown to have many characteristics similar to membranes derived from sensory neurons; both could mimic whole cells in stimulating Schwann cell division; both were inactivated by mild heat treatment and by trypsinization, and both elevated intracellular cyclic AMP concentrations in Schwann cells 16 h after addition of membranes. We conclude that PC12 cells will be a valuable source for the isolation of the neuronal cell surface component which controls proliferation of Schwann cells during development of the peripheral nervous system.
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spelling pubmed-21131322008-05-01 PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division J Cell Biol Articles Primary cultures of rat dorsal root ganglion Schwann cells were used to assay the efficacy of PC12 cells in stimulating Schwann cell proliferation. Co-cultures of PC12 cells and Schwann cells assayed by [3H]thymidine labeling followed by autoradiography showed proliferation of Schwann cells only where contact occurred between PC12 neurites and Schwann cells. Membranes derived from PC12 cells were shown to have many characteristics similar to membranes derived from sensory neurons; both could mimic whole cells in stimulating Schwann cell division; both were inactivated by mild heat treatment and by trypsinization, and both elevated intracellular cyclic AMP concentrations in Schwann cells 16 h after addition of membranes. We conclude that PC12 cells will be a valuable source for the isolation of the neuronal cell surface component which controls proliferation of Schwann cells during development of the peripheral nervous system. The Rockefeller University Press 1984-03-01 /pmc/articles/PMC2113132/ /pubmed/6321518 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
PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division
title PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division
title_full PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division
title_fullStr PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division
title_full_unstemmed PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division
title_short PC12 cells as a source of neurite-derived cell surface mitogen, which stimulates Schwann cell division
title_sort pc12 cells as a source of neurite-derived cell surface mitogen, which stimulates schwann cell division
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2113132/
https://www.ncbi.nlm.nih.gov/pubmed/6321518