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EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus
The mouse progenitor T lymphocyte (pro-T) cell line FTF1 binds in vitro to thymus blood vessels, the thymic capsule, and liver from newborn mice. A mAb, EA-1, raised against an embryonic mouse endothelial cell line, blocked adhesion. The antibody also interfered with pro-T cell adhesion to a thymus-...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1991
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289120/ https://www.ncbi.nlm.nih.gov/pubmed/1874787 |
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collection | PubMed |
description | The mouse progenitor T lymphocyte (pro-T) cell line FTF1 binds in vitro to thymus blood vessels, the thymic capsule, and liver from newborn mice. A mAb, EA-1, raised against an embryonic mouse endothelial cell line, blocked adhesion. The antibody also interfered with pro-T cell adhesion to a thymus-derived mouse endothelial cell line; it had no effect on the adhesion of mature T lymphocytes and myeloid cells. The antigen recognized by EA-1 is located on the vascular endothelium of various mouse tissues and absent on pro-T cells. EA-1 antibody precipitates molecules with apparent molecular weights of 110,000, 140,000, 160,000, and 200,000. Immunoclearing and binding-inhibition studies with antibodies against known adhesion molecules suggest that the EA-1 antigen is a novel adhesion molecule involved in colonization of the embryonic thymus by T cell progenitors. |
format | Text |
id | pubmed-2289120 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1991 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22891202008-05-01 EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus J Cell Biol Articles The mouse progenitor T lymphocyte (pro-T) cell line FTF1 binds in vitro to thymus blood vessels, the thymic capsule, and liver from newborn mice. A mAb, EA-1, raised against an embryonic mouse endothelial cell line, blocked adhesion. The antibody also interfered with pro-T cell adhesion to a thymus-derived mouse endothelial cell line; it had no effect on the adhesion of mature T lymphocytes and myeloid cells. The antigen recognized by EA-1 is located on the vascular endothelium of various mouse tissues and absent on pro-T cells. EA-1 antibody precipitates molecules with apparent molecular weights of 110,000, 140,000, 160,000, and 200,000. Immunoclearing and binding-inhibition studies with antibodies against known adhesion molecules suggest that the EA-1 antigen is a novel adhesion molecule involved in colonization of the embryonic thymus by T cell progenitors. The Rockefeller University Press 1991-09-01 /pmc/articles/PMC2289120/ /pubmed/1874787 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 EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus |
title | EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus |
title_full | EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus |
title_fullStr | EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus |
title_full_unstemmed | EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus |
title_short | EA-1, a novel adhesion molecule involved in the homing of progenitor T lymphocytes to the thymus |
title_sort | ea-1, a novel adhesion molecule involved in the homing of progenitor t lymphocytes to the thymus |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2289120/ https://www.ncbi.nlm.nih.gov/pubmed/1874787 |