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Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes

Pre-B cells in developing rabbits were identified by immunofluorescence as cells containing small amounts of cytoplasmic IgM (cIgM) but lacking surface immunoglobulin (sIg). During ontogeny the first pre-B cells appeared in fetal liver at 23 days gestation, 2 days before the appearance of sIgM+ B ly...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185044/
https://www.ncbi.nlm.nih.gov/pubmed/102726
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description Pre-B cells in developing rabbits were identified by immunofluorescence as cells containing small amounts of cytoplasmic IgM (cIgM) but lacking surface immunoglobulin (sIg). During ontogeny the first pre-B cells appeared in fetal liver at 23 days gestation, 2 days before the appearance of sIgM+ B lymphocytes. Pre-B cells were relatively frequent in fetal and adult bone marrow, but were not found in other tissues except rarely in fetal spleen. Allelic exclusion is apparently established at this early stage of development, because individual pre- B cells and B lymphocytes from heterozygous rabbits expressed only one of the alternative alleles in amounts sufficient for detection. Development of isotype diversity among rabbit B lymphocytes followed the general pattern seen in mouse and man. sIgM+ cells were detected before birth. Expression of sIgG was detected in neonatal rabbits on cells which were also sIgM+ but in older animals most sIgG+ cells lacked sIgM. Cells bearing sIgA were not found until 5-6 days of age, and had no other isotype on their surface.
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spelling pubmed-21850442008-04-17 Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes J Exp Med Articles Pre-B cells in developing rabbits were identified by immunofluorescence as cells containing small amounts of cytoplasmic IgM (cIgM) but lacking surface immunoglobulin (sIg). During ontogeny the first pre-B cells appeared in fetal liver at 23 days gestation, 2 days before the appearance of sIgM+ B lymphocytes. Pre-B cells were relatively frequent in fetal and adult bone marrow, but were not found in other tissues except rarely in fetal spleen. Allelic exclusion is apparently established at this early stage of development, because individual pre- B cells and B lymphocytes from heterozygous rabbits expressed only one of the alternative alleles in amounts sufficient for detection. Development of isotype diversity among rabbit B lymphocytes followed the general pattern seen in mouse and man. sIgM+ cells were detected before birth. Expression of sIgG was detected in neonatal rabbits on cells which were also sIgM+ but in older animals most sIgG+ cells lacked sIgM. Cells bearing sIgA were not found until 5-6 days of age, and had no other isotype on their surface. The Rockefeller University Press 1978-11-01 /pmc/articles/PMC2185044/ /pubmed/102726 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
Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes
title Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes
title_full Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes
title_fullStr Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes
title_full_unstemmed Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes
title_short Pre-B and B cells in rabbits. Ontogeny and allelic exclusion of kappa light chain genes
title_sort pre-b and b cells in rabbits. ontogeny and allelic exclusion of kappa light chain genes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2185044/
https://www.ncbi.nlm.nih.gov/pubmed/102726