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指数生长期血清对NIH-3T3细胞G1期转换的调控

Regulation of NIH-3T3 cell G1 phase transit by serum during exponential growth.

作者信息

DiSalvo C V, Zhang D, Jacobberger J W

机构信息

Department of Genetics, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

Cell Prolif. 1995 Sep;28(9):511-24. doi: 10.1111/j.1365-2184.1995.tb00089.x.

Abstract

The proliferation rate of mammalian cells is regulated normally in the G1 phase of the cell cycle. During this phase, it is convenient to assign positive and negative roles to the molecular programs that regulate the duration of G1 and the phase transition from G1 to S phase. Density-dependent inhibition of cellular proliferation results in an increase in the duration of G1. This form of regulation is due to both secreted factors and cell-cell contact. Serum is mitogenic to a variety of mammalian cell types. Because quiescent cells enter S phase as a result of serum addition to culture media, serum is usually regarded as a source of positive regulatory growth factors. We have measured the length of the G1, S and G2+M phases of NIH 3T3 cells during exponential growth as a function of cell density and serum concentration. The G1 length increases during exponential growth as a function of density while S and G2+M are relatively constant. Further, this increase in G1 phase time, or density mediated negative regulation, is inhibited by increasing serum concentration. This phenotype is saturable between 10% to 20% serum. Serum concentrations above 2.5% are able to increase the rate of cell cycling (decrease the G1 phase time) by inhibiting density dependent negative regulation of NIH 3T3.

摘要

哺乳动物细胞的增殖速率在细胞周期的G1期受到正常调控。在这个阶段,为调控G1期持续时间以及从G1期到S期的阶段转换的分子程序赋予正负作用是很方便的。细胞增殖的密度依赖性抑制导致G1期持续时间增加。这种调控形式既归因于分泌因子,也归因于细胞间接触。血清对多种哺乳动物细胞类型具有促有丝分裂作用。由于静止细胞因向培养基中添加血清而进入S期,血清通常被视为正性调节生长因子的来源。我们测量了指数生长期间NIH 3T3细胞的G1、S和G2+M期的时长,作为细胞密度和血清浓度的函数。在指数生长期间,G1期时长随着密度增加而增加,而S期和G2+M期相对恒定。此外,G1期时间的这种增加,即密度介导的负调控,会被血清浓度增加所抑制。这种表型在10%至20%血清之间达到饱和。高于2.5%的血清浓度能够通过抑制NIH 3T3细胞的密度依赖性负调控来提高细胞周期速率(缩短G1期时间)。

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