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CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS
The effects of thymectomy and thymus graft restoration upon the in vitro primary responses to alloantigens and PHA have been studied. It has been found that neonatal thymectomy substantially eliminates both PHA reactivity and responsiveness to alloantigens assayed in vitro in host spleen cell popula...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1971
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138885/ https://www.ncbi.nlm.nih.gov/pubmed/5539641 |
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author | Takiguchi, T. Adler, W. H. Smith, R. T. |
author_facet | Takiguchi, T. Adler, W. H. Smith, R. T. |
author_sort | Takiguchi, T. |
collection | PubMed |
description | The effects of thymectomy and thymus graft restoration upon the in vitro primary responses to alloantigens and PHA have been studied. It has been found that neonatal thymectomy substantially eliminates both PHA reactivity and responsiveness to alloantigens assayed in vitro in host spleen cell populations. Analysis of albumin density gradient-separated subpopulations of the spleen and thymus in such animals was also performed. It was found that the total and proportional representation of the individual density subpopulations was identical in neonatally thymectomized, in normal, and in thymectomized and thymus graft-restored animals. Therefore, thymectomized mice appear to retain a nonfunctioning, small, dense, lymphocyte population. Reconstitution of thymic-dependent in vitro reactivity was nearly complete when syngeneic, but not allogeneic or semisyngeneic thymus was employed. Occasional partial restoration did occur when F(1) thymus was employed, but never when allogeneic thymus was grafted. The grafted thymus contained PHA and alloantigen-reactive cells in a large, less dense B layer subpopulation, whereas the restored animals, as in the case of normals, showed these reactivities to be a property of a small, more dense cell population. |
format | Text |
id | pubmed-2138885 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1971 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21388852008-04-17 CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS Takiguchi, T. Adler, W. H. Smith, R. T. J Exp Med Article The effects of thymectomy and thymus graft restoration upon the in vitro primary responses to alloantigens and PHA have been studied. It has been found that neonatal thymectomy substantially eliminates both PHA reactivity and responsiveness to alloantigens assayed in vitro in host spleen cell populations. Analysis of albumin density gradient-separated subpopulations of the spleen and thymus in such animals was also performed. It was found that the total and proportional representation of the individual density subpopulations was identical in neonatally thymectomized, in normal, and in thymectomized and thymus graft-restored animals. Therefore, thymectomized mice appear to retain a nonfunctioning, small, dense, lymphocyte population. Reconstitution of thymic-dependent in vitro reactivity was nearly complete when syngeneic, but not allogeneic or semisyngeneic thymus was employed. Occasional partial restoration did occur when F(1) thymus was employed, but never when allogeneic thymus was grafted. The grafted thymus contained PHA and alloantigen-reactive cells in a large, less dense B layer subpopulation, whereas the restored animals, as in the case of normals, showed these reactivities to be a property of a small, more dense cell population. The Rockefeller University Press 1971-01-01 /pmc/articles/PMC2138885/ /pubmed/5539641 Text en Copyright © 1971 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 Takiguchi, T. Adler, W. H. Smith, R. T. CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS |
title | CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS |
title_full | CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS |
title_fullStr | CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS |
title_full_unstemmed | CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS |
title_short | CELLULAR RECOGNITION IN VITRO BY MOUSE LYMPHOCYTES : EFFECTS OF NEONATAL THYMECTOMY AND THYMUS GRAFT RESTORATION ON ALLOANTIGEN AND PHA STIMULATION OF WHOLE AND GRADIENT-SEPARATED SUBPOPULATIONS OF SPLEEN CELLS |
title_sort | cellular recognition in vitro by mouse lymphocytes : effects of neonatal thymectomy and thymus graft restoration on alloantigen and pha stimulation of whole and gradient-separated subpopulations of spleen cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138885/ https://www.ncbi.nlm.nih.gov/pubmed/5539641 |
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