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MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES

Cellular responses in vitro to H-2D region histocompatibility antigens were demonstrated to be under the genetic control of two or three (P = 0.013) independently segregating loci. The H-2 region itself accounts for one of these loci, however, its activity appears to be dependent upon an association...

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Autor principal: Plate, Janet M. D.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1974
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139574/
https://www.ncbi.nlm.nih.gov/pubmed/4131511
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author Plate, Janet M. D.
author_facet Plate, Janet M. D.
author_sort Plate, Janet M. D.
collection PubMed
description Cellular responses in vitro to H-2D region histocompatibility antigens were demonstrated to be under the genetic control of two or three (P = 0.013) independently segregating loci. The H-2 region itself accounts for one of these loci, however, its activity appears to be dependent upon an association with other non-H-2-associated genetic information. The ability to stimulate a response and to respond to that stimulus are two separate genetic functions in certain MLR combinations. The stimuli in our studies were products of the H-2D region and cell donors must differ at that region in order for a response to occur. The control of the level of responses was determined by other genetic material. Differences at these "response loci" were not necessary for the induction of a proliferative response in the mixed lymphocyte cultures.
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spelling pubmed-21395742008-04-17 MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES Plate, Janet M. D. J Exp Med Article Cellular responses in vitro to H-2D region histocompatibility antigens were demonstrated to be under the genetic control of two or three (P = 0.013) independently segregating loci. The H-2 region itself accounts for one of these loci, however, its activity appears to be dependent upon an association with other non-H-2-associated genetic information. The ability to stimulate a response and to respond to that stimulus are two separate genetic functions in certain MLR combinations. The stimuli in our studies were products of the H-2D region and cell donors must differ at that region in order for a response to occur. The control of the level of responses was determined by other genetic material. Differences at these "response loci" were not necessary for the induction of a proliferative response in the mixed lymphocyte cultures. The Rockefeller University Press 1974-04-01 /pmc/articles/PMC2139574/ /pubmed/4131511 Text en Copyright © 1974 by The Rockefeller University Press 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
Plate, Janet M. D.
MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES
title MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES
title_full MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES
title_fullStr MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES
title_full_unstemmed MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES
title_short MIXED LYMPHOCYTE CULTURE RESPONSES OF MICE : GENETIC ANALYSIS OF THE RESPONSES TOH-2D(d) SPECIFICITIES
title_sort mixed lymphocyte culture responses of mice : genetic analysis of the responses toh-2d(d) specificities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139574/
https://www.ncbi.nlm.nih.gov/pubmed/4131511
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