Stimulation of WI-38 cell cycle transit: Effect of serum concentration and cell density
Flow microfluorometry has been used to characterize the effects of serum concentration and cell density on the initiation of cell cycle transit of stationary phase (G0) human diploid fibroblasts (strain WI‐38). The concentration of serum used to stimulate these cultures had no effect on the time cel...
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Veröffentlicht in: | J. Cell. Physiol.; (United States) 1976-10, Vol.89 (2), p.251-257 |
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description | Flow microfluorometry has been used to characterize the effects of serum concentration and cell density on the initiation of cell cycle transit of stationary phase (G0) human diploid fibroblasts (strain WI‐38). The concentration of serum used to stimulate these cultures had no effect on the time cells began appearing in S (the DNA synthetic period), nor on the synchrony with which they moved around the cell cycle. However, as the serum concentration increased, the fraction of the stationary phase population released from G0 increased. Cell density modulated the ability of serum to stimulate cell cycle traverse. For example, at a cell density of 1.81 × 104 cells/cm2, 78% of the population was sensitive to serum stimulation; whereas, when the density was increased to 7.25 × 104 cells/cm2, only 27% of the population could be stimulated. This effect of cell density on the serum response is not simply the result of changing the ratio of serum concentration to cell density, but appears to reflect a true modulation of the population's sensitivity to serum stimulation. These results are consistent with the interpretation that the primary action of serum is to determine the transition of cells from a non‐cycling G0 state to a cycling state and that cell density determines the proportion of the population capable of undergoing this transition. |
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The concentration of serum used to stimulate these cultures had no effect on the time cells began appearing in S (the DNA synthetic period), nor on the synchrony with which they moved around the cell cycle. However, as the serum concentration increased, the fraction of the stationary phase population released from G0 increased. Cell density modulated the ability of serum to stimulate cell cycle traverse. For example, at a cell density of 1.81 × 104 cells/cm2, 78% of the population was sensitive to serum stimulation; whereas, when the density was increased to 7.25 × 104 cells/cm2, only 27% of the population could be stimulated. This effect of cell density on the serum response is not simply the result of changing the ratio of serum concentration to cell density, but appears to reflect a true modulation of the population's sensitivity to serum stimulation. These results are consistent with the interpretation that the primary action of serum is to determine the transition of cells from a non‐cycling G0 state to a cycling state and that cell density determines the proportion of the population capable of undergoing this transition.</description><identifier>ISSN: 0021-9541</identifier><identifier>EISSN: 1097-4652</identifier><identifier>DOI: 10.1002/jcp.1040890208</identifier><identifier>PMID: 972166</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>550300 - Cytology ; ANIMAL CELLS ; BASIC BIOLOGICAL SCIENCES ; Blood ; BLOOD SERUM ; Cell Count ; CELL CULTURES ; CELL CYCLE ; Cell Division ; CELL FLOW SYSTEMS ; Cell Line ; CONNECTIVE TISSUE CELLS ; DNA - biosynthesis ; FIBROBLASTS ; Mitosis ; SOMATIC CELLS</subject><ispartof>J. Cell. 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Cell. Physiol.; (United States)</title><addtitle>J. Cell. Physiol</addtitle><description>Flow microfluorometry has been used to characterize the effects of serum concentration and cell density on the initiation of cell cycle transit of stationary phase (G0) human diploid fibroblasts (strain WI‐38). The concentration of serum used to stimulate these cultures had no effect on the time cells began appearing in S (the DNA synthetic period), nor on the synchrony with which they moved around the cell cycle. However, as the serum concentration increased, the fraction of the stationary phase population released from G0 increased. Cell density modulated the ability of serum to stimulate cell cycle traverse. For example, at a cell density of 1.81 × 104 cells/cm2, 78% of the population was sensitive to serum stimulation; whereas, when the density was increased to 7.25 × 104 cells/cm2, only 27% of the population could be stimulated. This effect of cell density on the serum response is not simply the result of changing the ratio of serum concentration to cell density, but appears to reflect a true modulation of the population's sensitivity to serum stimulation. These results are consistent with the interpretation that the primary action of serum is to determine the transition of cells from a non‐cycling G0 state to a cycling state and that cell density determines the proportion of the population capable of undergoing this transition.</description><subject>550300 - Cytology</subject><subject>ANIMAL CELLS</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>Blood</subject><subject>BLOOD SERUM</subject><subject>Cell Count</subject><subject>CELL CULTURES</subject><subject>CELL CYCLE</subject><subject>Cell Division</subject><subject>CELL FLOW SYSTEMS</subject><subject>Cell Line</subject><subject>CONNECTIVE TISSUE CELLS</subject><subject>DNA - biosynthesis</subject><subject>FIBROBLASTS</subject><subject>Mitosis</subject><subject>SOMATIC CELLS</subject><issn>0021-9541</issn><issn>1097-4652</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1976</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkLlPHDEYxa2IJCyENhXFiCLdgK_xkQ6tOIWSSBwb0VjG81mYzLGMPQr73-NlEFEqKlt6v_f8_BD6SvA-wZgePLhlvnCsNKZYfUAzgrUsuajoBpplgJS64mQTbcX4gDHWmrHP6JOWlAgxQ4vLFNqxsSn0XdH7YnFWMlU4aJrCrVwDRRpsF0P6Xhx5Dy6tmQjD2Bau7xx0WX6x2q6eXDWs8dUX9NHbJsLO67mNro-Pruan5cXPk7P54UXpOOeqtFxLDVBXnAMGQpWsMLaaAuZCO0GcpUooJmrCvRRcM-5t_p6T1DMuvGPbaG_K7WMKJrqQwN3nal3uaiTjVFYkQ98maDn0jyPEZNoQ121tB_0YjWKVovmZDO5PoBv6GAfwZjmE1g4rQ7BZr23y2ubf2tmw-5o83rVQv-HTvFnWk_w3NLB6J8ycz3_9F11O3hATPL157fDHCMlkZRY_Tszt79Ob86vbSzNnz4DemMI</recordid><startdate>197610</startdate><enddate>197610</enddate><creator>Bartholomew, James C.</creator><creator>Neff, Nicola T.</creator><creator>Ross, Priscilla A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>197610</creationdate><title>Stimulation of WI-38 cell cycle transit: Effect of serum concentration and cell density</title><author>Bartholomew, James C. ; Neff, Nicola T. ; Ross, Priscilla A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4448-a4979eed544e0e1287500a92e0469c61ca286836d14f764934fa097c72f346fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1976</creationdate><topic>550300 - Cytology</topic><topic>ANIMAL CELLS</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Blood</topic><topic>BLOOD SERUM</topic><topic>Cell Count</topic><topic>CELL CULTURES</topic><topic>CELL CYCLE</topic><topic>Cell Division</topic><topic>CELL FLOW SYSTEMS</topic><topic>Cell Line</topic><topic>CONNECTIVE TISSUE CELLS</topic><topic>DNA - biosynthesis</topic><topic>FIBROBLASTS</topic><topic>Mitosis</topic><topic>SOMATIC CELLS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bartholomew, James C.</creatorcontrib><creatorcontrib>Neff, Nicola T.</creatorcontrib><creatorcontrib>Ross, Priscilla A.</creatorcontrib><creatorcontrib>Univ. of California, Berkeley</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>J. Cell. Physiol.; (United States)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bartholomew, James C.</au><au>Neff, Nicola T.</au><au>Ross, Priscilla A.</au><aucorp>Univ. of California, Berkeley</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stimulation of WI-38 cell cycle transit: Effect of serum concentration and cell density</atitle><jtitle>J. Cell. Physiol.; (United States)</jtitle><addtitle>J. Cell. Physiol</addtitle><date>1976-10</date><risdate>1976</risdate><volume>89</volume><issue>2</issue><spage>251</spage><epage>257</epage><pages>251-257</pages><issn>0021-9541</issn><eissn>1097-4652</eissn><abstract>Flow microfluorometry has been used to characterize the effects of serum concentration and cell density on the initiation of cell cycle transit of stationary phase (G0) human diploid fibroblasts (strain WI‐38). The concentration of serum used to stimulate these cultures had no effect on the time cells began appearing in S (the DNA synthetic period), nor on the synchrony with which they moved around the cell cycle. However, as the serum concentration increased, the fraction of the stationary phase population released from G0 increased. Cell density modulated the ability of serum to stimulate cell cycle traverse. For example, at a cell density of 1.81 × 104 cells/cm2, 78% of the population was sensitive to serum stimulation; whereas, when the density was increased to 7.25 × 104 cells/cm2, only 27% of the population could be stimulated. This effect of cell density on the serum response is not simply the result of changing the ratio of serum concentration to cell density, but appears to reflect a true modulation of the population's sensitivity to serum stimulation. These results are consistent with the interpretation that the primary action of serum is to determine the transition of cells from a non‐cycling G0 state to a cycling state and that cell density determines the proportion of the population capable of undergoing this transition.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>972166</pmid><doi>10.1002/jcp.1040890208</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 550300 - Cytology ANIMAL CELLS BASIC BIOLOGICAL SCIENCES Blood BLOOD SERUM Cell Count CELL CULTURES CELL CYCLE Cell Division CELL FLOW SYSTEMS Cell Line CONNECTIVE TISSUE CELLS DNA - biosynthesis FIBROBLASTS Mitosis SOMATIC CELLS |
title | Stimulation of WI-38 cell cycle transit: Effect of serum concentration and cell density |
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