Literature DB >> 2369933

Long-term growth of diploid human fibroblasts in low serum media.

C Wistrom1, B Villeponteau.   

Abstract

Hayflick and Moorhead demonstrated that diploid human fibroblasts have a limited life span when grown in media containing 10% bovine calf sera. Recent experiments have suggested that antigrowth factors in serum may be a potential contributor to the limited proliferative capacity of normal diploid cells. To reduce the concentration of inhibitory serum factors 10-fold, MRC-5 diploid fibroblasts were cultured in media with only 1% serum. Long-term culture in 1% serum requires the addition of purified growth factors to sustain proliferation. Although there are dramatic changes in cell morphology, we find that the long-term division potential of MRC-5 cells cultured in media containing 1% serum and growth factors differs little from that found with cells cultured in 10% serum. In contrast, MRC-5 cells cultured in 10% serum and added growth factors have a somewhat extended life span. These results suggest that negative growth factors are not responsible for the limited proliferative capacity of in vitro cultured human fibroblasts. Moreover, the evidence that human fibroblasts can undergo major changes in cell morphology and still retain a normal life span raises questions about the validity of using morphological changes as indicators of cellular senescence.

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Year:  1990        PMID: 2369933     DOI: 10.1016/0531-5565(90)90040-9

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


  3 in total

1.  Low-serum medium development for human diploid fibroblast microcarrier cultures.

Authors:  S P Forestell; N Kalogerakis; L A Behie
Journal:  Appl Microbiol Biotechnol       Date:  1992-11       Impact factor: 4.813

2.  Evaluation of royal jelly as an alternative to fetal bovine serum in cell culture using cell proliferation assays and live cell imaging.

Authors:  Marahaini Musa; Nurul Fatihah Mohamad Nasir; Kannan Ponnuraj Thirumulu
Journal:  Afr J Tradit Complement Altern Med       Date:  2013-11-02

3.  Premature senescence involving p53 and p16 is activated in response to constitutive MEK/MAPK mitogenic signaling.

Authors:  A W Lin; M Barradas; J C Stone; L van Aelst; M Serrano; S W Lowe
Journal:  Genes Dev       Date:  1998-10-01       Impact factor: 11.361

  3 in total

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