Cargando…

THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE

A single, functional, mitotically quiescent chondrocyte may be induced to reenter the mitotic cyde, and produce a progeny of over 10(11) cells. Sessile, adherent, polygonal cells deposit matrix, whereas amoeboid, dispersed, flattened fibroblastic cells do not. The prior synthetic history of a cell i...

Descripción completa

Detalles Bibliográficos
Autores principales: Chacko, S., Abbott, J., Holtzer, S., Holtzer, H.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1969
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138686/
https://www.ncbi.nlm.nih.gov/pubmed/5795101
_version_ 1782143621119606784
author Chacko, S.
Abbott, J.
Holtzer, S.
Holtzer, H.
author_facet Chacko, S.
Abbott, J.
Holtzer, S.
Holtzer, H.
author_sort Chacko, S.
collection PubMed
description A single, functional, mitotically quiescent chondrocyte may be induced to reenter the mitotic cyde, and produce a progeny of over 10(11) cells. Sessile, adherent, polygonal cells deposit matrix, whereas amoeboid, dispersed, flattened fibroblastic cells do not. The prior synthetic history of a cell is of greater importance in determining whether the characteristic chondrogenic phenotype will be expressed, rather than growth in "permissive" or "nonpermissive" medium. Clonal conditions select for stem-like cells, some of whose progeny may become polygonal chondrocytes. The retention of the characteristic chondrogenic phenotype in vitro is favored by pruning the dedifferentiated chondrocytes which arise in these cultures. Dedifferentiated chondrocytes interfere with the deposition and synthesis of chondroitin sulfate by neighboring functional chondrocytes. Possible mechanisms are proposed to explain this type of cell-cell or cell exudate interference. If the progeny of a single, genetically programmed chondrocyte may or may not synthesize chondroitin sulfate, then extragenic sites in the cytoplasm or cell surface must influence the decision as to which cluster of "luxur" molecules the cell will synthesize.
format Text
id pubmed-2138686
institution National Center for Biotechnology Information
language English
publishDate 1969
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-21386862008-04-17 THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE Chacko, S. Abbott, J. Holtzer, S. Holtzer, H. J Exp Med Article A single, functional, mitotically quiescent chondrocyte may be induced to reenter the mitotic cyde, and produce a progeny of over 10(11) cells. Sessile, adherent, polygonal cells deposit matrix, whereas amoeboid, dispersed, flattened fibroblastic cells do not. The prior synthetic history of a cell is of greater importance in determining whether the characteristic chondrogenic phenotype will be expressed, rather than growth in "permissive" or "nonpermissive" medium. Clonal conditions select for stem-like cells, some of whose progeny may become polygonal chondrocytes. The retention of the characteristic chondrogenic phenotype in vitro is favored by pruning the dedifferentiated chondrocytes which arise in these cultures. Dedifferentiated chondrocytes interfere with the deposition and synthesis of chondroitin sulfate by neighboring functional chondrocytes. Possible mechanisms are proposed to explain this type of cell-cell or cell exudate interference. If the progeny of a single, genetically programmed chondrocyte may or may not synthesize chondroitin sulfate, then extragenic sites in the cytoplasm or cell surface must influence the decision as to which cluster of "luxur" molecules the cell will synthesize. The Rockefeller University Press 1969-08-01 /pmc/articles/PMC2138686/ /pubmed/5795101 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
Chacko, S.
Abbott, J.
Holtzer, S.
Holtzer, H.
THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE
title THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE
title_full THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE
title_fullStr THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE
title_full_unstemmed THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE
title_short THE LOSS OF PHENOTYPIC TRAITS BY DIFFERENTIATED CELLS : VI. BEHAVIOR OF THE PROGENY OF A SINGLE CHONDROCYTE
title_sort loss of phenotypic traits by differentiated cells : vi. behavior of the progeny of a single chondrocyte
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2138686/
https://www.ncbi.nlm.nih.gov/pubmed/5795101
work_keys_str_mv AT chackos thelossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT abbottj thelossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT holtzers thelossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT holtzerh thelossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT chackos lossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT abbottj lossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT holtzers lossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte
AT holtzerh lossofphenotypictraitsbydifferentiatedcellsvibehavioroftheprogenyofasinglechondrocyte