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In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice
We have found cell surface expression of an E alpha molecule in recombinant and transgenic mouse strains lacking an E beta molecule. Flow cytometry has shown low level expression of E alpha in B10.RQB3 (I- AqEk alpha) and B10.RFB2 (I-AfEk alpha) mice. We have also found that B10.Q (H-2q) mice can ex...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1989
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189450/ https://www.ncbi.nlm.nih.gov/pubmed/2788700 |
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collection | PubMed |
description | We have found cell surface expression of an E alpha molecule in recombinant and transgenic mouse strains lacking an E beta molecule. Flow cytometry has shown low level expression of E alpha in B10.RQB3 (I- AqEk alpha) and B10.RFB2 (I-AfEk alpha) mice. We have also found that B10.Q (H-2q) mice can express the Ek alpha transgene. Since these strains do not have functional E beta chains, we propose that the E alpha A beta hybrid dimers are formed in low numbers and can be picked up by FACS analysis. So far we have not been able to identify these hybrid molecules by cytotoxicity or immunoprecipitation. The E alpha/A beta molecule can function in vivo during thymic selection in the clonal deletion of two V beta TCR subsets, V beta 11 and V beta 6, which have been shown to interact with the intact I-E molecule. |
format | Text |
id | pubmed-2189450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1989 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21894502008-04-17 In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice J Exp Med Articles We have found cell surface expression of an E alpha molecule in recombinant and transgenic mouse strains lacking an E beta molecule. Flow cytometry has shown low level expression of E alpha in B10.RQB3 (I- AqEk alpha) and B10.RFB2 (I-AfEk alpha) mice. We have also found that B10.Q (H-2q) mice can express the Ek alpha transgene. Since these strains do not have functional E beta chains, we propose that the E alpha A beta hybrid dimers are formed in low numbers and can be picked up by FACS analysis. So far we have not been able to identify these hybrid molecules by cytotoxicity or immunoprecipitation. The E alpha/A beta molecule can function in vivo during thymic selection in the clonal deletion of two V beta TCR subsets, V beta 11 and V beta 6, which have been shown to interact with the intact I-E molecule. The Rockefeller University Press 1989-09-01 /pmc/articles/PMC2189450/ /pubmed/2788700 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 In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice |
title | In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice |
title_full | In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice |
title_fullStr | In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice |
title_full_unstemmed | In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice |
title_short | In vivo expression and function of hybrid Ia dimers (E alpha A beta) in recombinant and transgenic mice |
title_sort | in vivo expression and function of hybrid ia dimers (e alpha a beta) in recombinant and transgenic mice |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2189450/ https://www.ncbi.nlm.nih.gov/pubmed/2788700 |