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GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE
Erythropoietic cells of two unrelated strains, C3H (or C3Hf) and C57BL/6, can coexist throughout hematopoiesis in allophenic mice experimentally produced from aggregated, undifferentiated blastomeres of separate genotypes. The presence of two red cell genotypes in these circumstances signifies that...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
1969
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138637/ https://www.ncbi.nlm.nih.gov/pubmed/5778785 |
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author | Mintz, Beatrice Palm, Joy |
author_facet | Mintz, Beatrice Palm, Joy |
author_sort | Mintz, Beatrice |
collection | PubMed |
description | Erythropoietic cells of two unrelated strains, C3H (or C3Hf) and C57BL/6, can coexist throughout hematopoiesis in allophenic mice experimentally produced from aggregated, undifferentiated blastomeres of separate genotypes. The presence of two red cell genotypes in these circumstances signifies that the erythroid population must normally be multiclonal, i.e., derived mitotically from at least two genetically determined cells. The two strains were detected by hemagglutination and absorption tests of erythrocytes for the specific histocompatibility antigens dictated by the H-2(k) and H-2(b) alleles. Of 34 C3H(f) ↔ C57BL/6 allophenics tested, 16 had both red cell types; the remaining 18 showed only C3H or C57 red cells and included 12 mice with both cell strains present in some other tissues. All animals with evidence of two H-2 phenotypes among circulating erythrocytes were permanently immunologically tolerant of both antigenic types and remained free of runt disease. They lived a full lifespan, up to 2 yr 7½ months of age. The data suggest a possible specific selective advantage of C57BL/6 over C3H erythropoietic tissue. There is considerable individual variability, not only in proportions of antigenically distinct erythrocytes, but also in strain composition of other tissues in the same animals. A broad spectrum of distinctive situations is found, in which parameters are varied within or outside of the circulatory system. Allophenic mice can therefore serve as investigative tools for entirely new kinds of experimental studies of gene control mechanisms and blood physiology in normal hematopoiesis and in a number of hereditary blood diseases. |
format | Text |
id | pubmed-2138637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1969 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21386372008-04-17 GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE Mintz, Beatrice Palm, Joy J Exp Med Article Erythropoietic cells of two unrelated strains, C3H (or C3Hf) and C57BL/6, can coexist throughout hematopoiesis in allophenic mice experimentally produced from aggregated, undifferentiated blastomeres of separate genotypes. The presence of two red cell genotypes in these circumstances signifies that the erythroid population must normally be multiclonal, i.e., derived mitotically from at least two genetically determined cells. The two strains were detected by hemagglutination and absorption tests of erythrocytes for the specific histocompatibility antigens dictated by the H-2(k) and H-2(b) alleles. Of 34 C3H(f) ↔ C57BL/6 allophenics tested, 16 had both red cell types; the remaining 18 showed only C3H or C57 red cells and included 12 mice with both cell strains present in some other tissues. All animals with evidence of two H-2 phenotypes among circulating erythrocytes were permanently immunologically tolerant of both antigenic types and remained free of runt disease. They lived a full lifespan, up to 2 yr 7½ months of age. The data suggest a possible specific selective advantage of C57BL/6 over C3H erythropoietic tissue. There is considerable individual variability, not only in proportions of antigenically distinct erythrocytes, but also in strain composition of other tissues in the same animals. A broad spectrum of distinctive situations is found, in which parameters are varied within or outside of the circulatory system. Allophenic mice can therefore serve as investigative tools for entirely new kinds of experimental studies of gene control mechanisms and blood physiology in normal hematopoiesis and in a number of hereditary blood diseases. The Rockefeller University Press 1969-05-01 /pmc/articles/PMC2138637/ /pubmed/5778785 Text en Copyright © 1969 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 Mintz, Beatrice Palm, Joy GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE |
title | GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE |
title_full | GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE |
title_fullStr | GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE |
title_full_unstemmed | GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE |
title_short | GENE CONTROL OF HEMATOPOIESIS : I. ERYTHROCYTE MOSAICISM AND PERMANENT IMMUNOLOGICAL TOLERANCE IN ALLOPHENIC MICE |
title_sort | gene control of hematopoiesis : i. erythrocyte mosaicism and permanent immunological tolerance in allophenic mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138637/ https://www.ncbi.nlm.nih.gov/pubmed/5778785 |
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