Cargando…
Tenascin Supports Lymphocyte Rolling
Tenascin is a large extracellular matrix molecule expressed at specific sites in the adult, including immune system tissues such as the bone marrow, thymus, spleen, and T cell areas of lymph nodes. Tenascin has been reported to have both adhesive and anti-adhesive effects in static assays. We report...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1997
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139881/ https://www.ncbi.nlm.nih.gov/pubmed/9151679 |
_version_ | 1782143899456765952 |
---|---|
author | Clark, Rachael A. Erickson, Harold P. Springer, Timothy A. |
author_facet | Clark, Rachael A. Erickson, Harold P. Springer, Timothy A. |
author_sort | Clark, Rachael A. |
collection | PubMed |
description | Tenascin is a large extracellular matrix molecule expressed at specific sites in the adult, including immune system tissues such as the bone marrow, thymus, spleen, and T cell areas of lymph nodes. Tenascin has been reported to have both adhesive and anti-adhesive effects in static assays. We report here that tenascin supports the tethering and rolling of lymphocytes and lymphoblastic cell lines under flow conditions. Binding was calcium dependent and was not inhibited by treatment of lymphocytes with O-glycoprotease or a panel of glycosidases including neuraminidase and heparitinase but was inhibited by treatment of cells with proteinase K. Binding was to the fibrinogen-like terminal domain of tenascin as determined by antibody blocking studies and binding to recombinant tenascin proteins. When compared to rolling of the same cell type on E-selectin, rolling on tenascin was found to be smoother at all shear stresses tested, suggesting that cells formed a larger number of bonds on the tenascin substrate than on the E-selectin substrate. When protein plating densities were adjusted to give similar profiles of cell detachment under increasing shears, the density of tenascin was 8.5-fold greater than that of E-selectin. Binding to tenascin was not dependent on any molecules previously identified as tenascin receptors and is likely to involve a novel tenascin receptor on lymphocytes. We postulate that the ability of tenascin to support lymphocyte rolling may reflect its ability to support cell migration and that this interaction may be used by lymphocytes migrating through secondary lymphoid organs. |
format | Text |
id | pubmed-2139881 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21398812008-05-01 Tenascin Supports Lymphocyte Rolling Clark, Rachael A. Erickson, Harold P. Springer, Timothy A. J Cell Biol Article Tenascin is a large extracellular matrix molecule expressed at specific sites in the adult, including immune system tissues such as the bone marrow, thymus, spleen, and T cell areas of lymph nodes. Tenascin has been reported to have both adhesive and anti-adhesive effects in static assays. We report here that tenascin supports the tethering and rolling of lymphocytes and lymphoblastic cell lines under flow conditions. Binding was calcium dependent and was not inhibited by treatment of lymphocytes with O-glycoprotease or a panel of glycosidases including neuraminidase and heparitinase but was inhibited by treatment of cells with proteinase K. Binding was to the fibrinogen-like terminal domain of tenascin as determined by antibody blocking studies and binding to recombinant tenascin proteins. When compared to rolling of the same cell type on E-selectin, rolling on tenascin was found to be smoother at all shear stresses tested, suggesting that cells formed a larger number of bonds on the tenascin substrate than on the E-selectin substrate. When protein plating densities were adjusted to give similar profiles of cell detachment under increasing shears, the density of tenascin was 8.5-fold greater than that of E-selectin. Binding to tenascin was not dependent on any molecules previously identified as tenascin receptors and is likely to involve a novel tenascin receptor on lymphocytes. We postulate that the ability of tenascin to support lymphocyte rolling may reflect its ability to support cell migration and that this interaction may be used by lymphocytes migrating through secondary lymphoid organs. The Rockefeller University Press 1997-05-05 /pmc/articles/PMC2139881/ /pubmed/9151679 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 | Article Clark, Rachael A. Erickson, Harold P. Springer, Timothy A. Tenascin Supports Lymphocyte Rolling |
title | Tenascin Supports Lymphocyte Rolling |
title_full | Tenascin Supports Lymphocyte Rolling |
title_fullStr | Tenascin Supports Lymphocyte Rolling |
title_full_unstemmed | Tenascin Supports Lymphocyte Rolling |
title_short | Tenascin Supports Lymphocyte Rolling |
title_sort | tenascin supports lymphocyte rolling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139881/ https://www.ncbi.nlm.nih.gov/pubmed/9151679 |
work_keys_str_mv | AT clarkrachaela tenascinsupportslymphocyterolling AT ericksonharoldp tenascinsupportslymphocyterolling AT springertimothya tenascinsupportslymphocyterolling |