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Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation

Experimental evidence is presented that supports a cell cycle model showing that there are five distinct biological processes involved in proadipocyte differentiation. These include: (a) growth arrest at a distinct state in the G1 phase of the cell cycle; (b) nonterminal differentiation; (c) termina...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1982
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112887/
https://www.ncbi.nlm.nih.gov/pubmed/6809770
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description Experimental evidence is presented that supports a cell cycle model showing that there are five distinct biological processes involved in proadipocyte differentiation. These include: (a) growth arrest at a distinct state in the G1 phase of the cell cycle; (b) nonterminal differentiation; (c) terminal differentiation; (d) loss of the differentiated phenotype; and (e) reinitiation of cell proliferation. Each of these events is shown to be regulated by specific human plasma components or other physiological factors. At two states designated GD and GD', coupling of growth arrest and differentiation is shown to occur. We propose that these mechanisms for the coupling of growth arrest and differentiation are physiologically significant and mimic the regulatory processes that control stem cell proliferation in vivo.
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spelling pubmed-21128872008-05-01 Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation J Cell Biol Articles Experimental evidence is presented that supports a cell cycle model showing that there are five distinct biological processes involved in proadipocyte differentiation. These include: (a) growth arrest at a distinct state in the G1 phase of the cell cycle; (b) nonterminal differentiation; (c) terminal differentiation; (d) loss of the differentiated phenotype; and (e) reinitiation of cell proliferation. Each of these events is shown to be regulated by specific human plasma components or other physiological factors. At two states designated GD and GD', coupling of growth arrest and differentiation is shown to occur. We propose that these mechanisms for the coupling of growth arrest and differentiation are physiologically significant and mimic the regulatory processes that control stem cell proliferation in vivo. The Rockefeller University Press 1982-08-01 /pmc/articles/PMC2112887/ /pubmed/6809770 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
Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation
title Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation
title_full Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation
title_fullStr Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation
title_full_unstemmed Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation
title_short Coupling of proadipocyte growth arrest and differentiation. II. A cell cycle model for the physiological control of cell proliferation
title_sort coupling of proadipocyte growth arrest and differentiation. ii. a cell cycle model for the physiological control of cell proliferation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2112887/
https://www.ncbi.nlm.nih.gov/pubmed/6809770