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Glypican-1, phosphacan/receptor protein-tyrosine phosphatase-ζ/β and its ligand, tenascin-C, are expressed by neural stem cells and neural cells derived from embryonic stem cells
The heparan sulfate proteoglycan glypican-1, the chondroitin sulfate proteoglycan phosphacan/RPTP (receptor protein-tyrosine phosphatase)-ζ/β and the extracellular matrix protein tenascin-C were all found to be expressed by neural stem cells and by neural cells derived from them. Expression of prote...
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Formato: | Texto |
Lenguaje: | English |
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American Society for Neurochemistry
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2914431/ https://www.ncbi.nlm.nih.gov/pubmed/20689858 http://dx.doi.org/10.1042/AN20100001 |
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author | Abaskharoun, Mary Bellemare, Marie Lau, Elizabeth Margolis, Richard U |
author_facet | Abaskharoun, Mary Bellemare, Marie Lau, Elizabeth Margolis, Richard U |
author_sort | Abaskharoun, Mary |
collection | PubMed |
description | The heparan sulfate proteoglycan glypican-1, the chondroitin sulfate proteoglycan phosphacan/RPTP (receptor protein-tyrosine phosphatase)-ζ/β and the extracellular matrix protein tenascin-C were all found to be expressed by neural stem cells and by neural cells derived from them. Expression of proteoglycans and tenascin-C increased after retinoic acid induction of SSEA1-positive ES (embryonic stem) cells to nestin-positive neural stem cells, and after neural differentiation, proteoglycans and tenascin-C are expressed by both neurons and astrocytes, where they surround cell bodies and processes and in certain cases show distinctive expression patterns. With the exception of tenascin-C (whose expression may decrease somewhat), expression levels do not change noticeably during the following 2 weeks in culture. The significant expression, by neural stem cells and neurons and astrocytes derived from them, of two major heparan sulfate and chondroitin sulfate proteoglycans of nervous tissue and of tenascin-C, a high-affinity ligand of phosphacan/RPTP-ζ/β, indicates that an understanding of their specific functional roles in stem cell neurobiology will be important for the therapeutic application of this new technology in facilitating nervous tissue repair and regeneration. |
format | Text |
id | pubmed-2914431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Society for Neurochemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-29144312010-08-04 Glypican-1, phosphacan/receptor protein-tyrosine phosphatase-ζ/β and its ligand, tenascin-C, are expressed by neural stem cells and neural cells derived from embryonic stem cells Abaskharoun, Mary Bellemare, Marie Lau, Elizabeth Margolis, Richard U ASN Neuro Research Article The heparan sulfate proteoglycan glypican-1, the chondroitin sulfate proteoglycan phosphacan/RPTP (receptor protein-tyrosine phosphatase)-ζ/β and the extracellular matrix protein tenascin-C were all found to be expressed by neural stem cells and by neural cells derived from them. Expression of proteoglycans and tenascin-C increased after retinoic acid induction of SSEA1-positive ES (embryonic stem) cells to nestin-positive neural stem cells, and after neural differentiation, proteoglycans and tenascin-C are expressed by both neurons and astrocytes, where they surround cell bodies and processes and in certain cases show distinctive expression patterns. With the exception of tenascin-C (whose expression may decrease somewhat), expression levels do not change noticeably during the following 2 weeks in culture. The significant expression, by neural stem cells and neurons and astrocytes derived from them, of two major heparan sulfate and chondroitin sulfate proteoglycans of nervous tissue and of tenascin-C, a high-affinity ligand of phosphacan/RPTP-ζ/β, indicates that an understanding of their specific functional roles in stem cell neurobiology will be important for the therapeutic application of this new technology in facilitating nervous tissue repair and regeneration. American Society for Neurochemistry 2010-07-30 /pmc/articles/PMC2914431/ /pubmed/20689858 http://dx.doi.org/10.1042/AN20100001 Text en © 2010 The Author(s). http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial Licence (http://creativecommons.org/licenses/by-nc/2.5/) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Abaskharoun, Mary Bellemare, Marie Lau, Elizabeth Margolis, Richard U Glypican-1, phosphacan/receptor protein-tyrosine phosphatase-ζ/β and its ligand, tenascin-C, are expressed by neural stem cells and neural cells derived from embryonic stem cells |
title | Glypican-1, phosphacan/receptor protein-tyrosine
phosphatase-ζ/β and its ligand, tenascin-C, are expressed
by neural stem cells and neural cells derived from embryonic stem cells |
title_full | Glypican-1, phosphacan/receptor protein-tyrosine
phosphatase-ζ/β and its ligand, tenascin-C, are expressed
by neural stem cells and neural cells derived from embryonic stem cells |
title_fullStr | Glypican-1, phosphacan/receptor protein-tyrosine
phosphatase-ζ/β and its ligand, tenascin-C, are expressed
by neural stem cells and neural cells derived from embryonic stem cells |
title_full_unstemmed | Glypican-1, phosphacan/receptor protein-tyrosine
phosphatase-ζ/β and its ligand, tenascin-C, are expressed
by neural stem cells and neural cells derived from embryonic stem cells |
title_short | Glypican-1, phosphacan/receptor protein-tyrosine
phosphatase-ζ/β and its ligand, tenascin-C, are expressed
by neural stem cells and neural cells derived from embryonic stem cells |
title_sort | glypican-1, phosphacan/receptor protein-tyrosine
phosphatase-ζ/β and its ligand, tenascin-c, are expressed
by neural stem cells and neural cells derived from embryonic stem cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2914431/ https://www.ncbi.nlm.nih.gov/pubmed/20689858 http://dx.doi.org/10.1042/AN20100001 |
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