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MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES

The ultrastructural features of B-, T-, and surface Ig(sIg)-bearing cells have been studied on cell suspensions from lymphoid organs of mice at different stages of immunization. The cells were identified by exposure to rabbit antibodies against mouse-specific lymphocyte antigens (MSLA) or brain-asso...

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Autores principales: Matter, A., Lisowska-Bernstein, B., Ryser, J. E., Lamelin, J.-P., Vassalli, P.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1972
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139311/
https://www.ncbi.nlm.nih.gov/pubmed/4563148
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author Matter, A.
Lisowska-Bernstein, B.
Ryser, J. E.
Lamelin, J.-P.
Vassalli, P.
author_facet Matter, A.
Lisowska-Bernstein, B.
Ryser, J. E.
Lamelin, J.-P.
Vassalli, P.
author_sort Matter, A.
collection PubMed
description The ultrastructural features of B-, T-, and surface Ig(sIg)-bearing cells have been studied on cell suspensions from lymphoid organs of mice at different stages of immunization. The cells were identified by exposure to rabbit antibodies against mouse-specific lymphocyte antigens (MSLA) or brain-associated θ antigen (BAθ) for T cells, mouse-specific bone marrow-derived lymphocyte antigens (MBLA) for B cells, and mouse Ig for sIg-bearing cells. The rabbit antibodies fixed on the cell surfaces were detected by peroxidase-labeled sheep anti-rabbit Ig antibodies or by a "bridge" technique using southern bean mosaic virus or bacteriophage T4 as the final markers. In some experiments, short-lived lymphoid cells were labeled in vivo with repeated tritiated thymidine and the ultrastructural detection of their surface antigens was combined with radioautography. MBLA+ lymphoid cells showed a whole range of ultrastructural patterns. Most were small and medium-sized lymphocytes with a clear cytoplasm containing mono- and polyribosomes, but they comprised also blasts and large cells with various amounts of endoplasmic reticulum, as well as plasma cells at different stages of maturation. sIg-bearing cells appeared to be identical with MBLA+ cells, except that sIg was less easily detectable on large blasts, and only very rarely observed on plasma cells. MSLA+ and BAθ+ cells fell into three categories. One of them (T(1) cells) consisted of small to medium-sized lymphocytes with a clear cytoplasm and few organelles, mostly monoribosomes. A second consisted of large cells (T(2) cells) characterized by numerous polyribosomes often in a "rosette"-like pattern, occasional dark, membrane-bound granules, and a developing "filamentous network." The third, very characteristic type, (T(3) cells) was represented by dark small to medium-sized lymphocytes, usually containing large amounts of closely packed ribosomes and showing a striking accumulation of filamentous network, often condensed in large areas devoid of cell organelles. This filamentous network appeared to correspond to the cytochalasin B-sensitive system of microfilaments found in other cells and considered to be one of the contractile elements of the cell. The T(3) lymphocytes showed frequently vesicles suggestive of a strong pinocytic activity, and assumed a variety of shapes, including uropods. Evidence is presented that T(1) lymphocytes represent "virgin" T cells, T(2) "activated," and T(3) "differentiated" lymphocytes.
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spelling pubmed-21393112008-04-17 MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES Matter, A. Lisowska-Bernstein, B. Ryser, J. E. Lamelin, J.-P. Vassalli, P. J Exp Med Article The ultrastructural features of B-, T-, and surface Ig(sIg)-bearing cells have been studied on cell suspensions from lymphoid organs of mice at different stages of immunization. The cells were identified by exposure to rabbit antibodies against mouse-specific lymphocyte antigens (MSLA) or brain-associated θ antigen (BAθ) for T cells, mouse-specific bone marrow-derived lymphocyte antigens (MBLA) for B cells, and mouse Ig for sIg-bearing cells. The rabbit antibodies fixed on the cell surfaces were detected by peroxidase-labeled sheep anti-rabbit Ig antibodies or by a "bridge" technique using southern bean mosaic virus or bacteriophage T4 as the final markers. In some experiments, short-lived lymphoid cells were labeled in vivo with repeated tritiated thymidine and the ultrastructural detection of their surface antigens was combined with radioautography. MBLA+ lymphoid cells showed a whole range of ultrastructural patterns. Most were small and medium-sized lymphocytes with a clear cytoplasm containing mono- and polyribosomes, but they comprised also blasts and large cells with various amounts of endoplasmic reticulum, as well as plasma cells at different stages of maturation. sIg-bearing cells appeared to be identical with MBLA+ cells, except that sIg was less easily detectable on large blasts, and only very rarely observed on plasma cells. MSLA+ and BAθ+ cells fell into three categories. One of them (T(1) cells) consisted of small to medium-sized lymphocytes with a clear cytoplasm and few organelles, mostly monoribosomes. A second consisted of large cells (T(2) cells) characterized by numerous polyribosomes often in a "rosette"-like pattern, occasional dark, membrane-bound granules, and a developing "filamentous network." The third, very characteristic type, (T(3) cells) was represented by dark small to medium-sized lymphocytes, usually containing large amounts of closely packed ribosomes and showing a striking accumulation of filamentous network, often condensed in large areas devoid of cell organelles. This filamentous network appeared to correspond to the cytochalasin B-sensitive system of microfilaments found in other cells and considered to be one of the contractile elements of the cell. The T(3) lymphocytes showed frequently vesicles suggestive of a strong pinocytic activity, and assumed a variety of shapes, including uropods. Evidence is presented that T(1) lymphocytes represent "virgin" T cells, T(2) "activated," and T(3) "differentiated" lymphocytes. The Rockefeller University Press 1972-10-31 /pmc/articles/PMC2139311/ /pubmed/4563148 Text en Copyright © 1972 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
Matter, A.
Lisowska-Bernstein, B.
Ryser, J. E.
Lamelin, J.-P.
Vassalli, P.
MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES
title MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES
title_full MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES
title_fullStr MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES
title_full_unstemmed MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES
title_short MOUSE THYMUS-INDEPENDENT AND THYMUS-DERIVED LYMPHOID CELLS : II. ULTRASTRUCTURAL STUDIES
title_sort mouse thymus-independent and thymus-derived lymphoid cells : ii. ultrastructural studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139311/
https://www.ncbi.nlm.nih.gov/pubmed/4563148
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