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密度依赖性生长停滞是WI-38细胞中的一个两阶段过程的证据。

Evidence that density-dependent growth arrest is a two-stage process in WI-38 cells.

作者信息

Owen T A, Carter R, Whitman M M, Soprano D R, Soprano K J

机构信息

Department of Microbiology and Immunology, Temple University School of Medicine, Philadelphia, Pennsylvania 19140.

出版信息

J Cell Physiol. 1990 Jan;142(1):137-48. doi: 10.1002/jcp.1041420117.

Abstract

It was the goal of this study to determine whether during long-term quiescence WI-38 cells gradually lose labile components which then need to be resynthesized before a stimulated cell can progress through G-1 and enter S. The metabolic and molecular status of WI-38 cells was systematically analyzed as they entered and were maintained for an extended period of time in a state of density-dependent growth arrest. Our results indicate that growth arrest in WI-38 cells can be divided into two stages. The first, which we call "early" growth arrest, occurs during the first 7-10 days following cessation of DNA synthesis and mitosis. It is characterized by few biochemical changes compared to actively proliferating cells. During this period of early growth arrest cells do not exhibit a prolongation of the prereplicative stage following serum stimulation. In contrast, WI-38 cells growth arrested for 10-20 days exhibit a number of changes at the molecular and biochemical level (i.e., a twofold decrease in total protein and total RNA content, and decreased levels of most proteins, but an increased amount of fibronectin and collagen). Also, quiescent WI-38 cells stimulated at any time during "later" or "deep" growth arrest do exhibit a prolonged prereplicative phase. Although changes were also observed in the patterns of expression of ten representative growth-associated genes (i.e., histone H-3, p53, c-Ha-ras, 2A9/calcyclin, 4F1/vimentin, LDL-receptor, insulin receptor, collagen, and fibronectin), these occurred mostly at the time when the cells ceased synthesis of DNA and mitosis and became quiescent. No changes in the steady-state levels of the growth-associated transcripts analyzed occurred while the cells were maintained in the growth-arrested state. Thus, these experiments show that although WI-38 cells do cease to incorporate thymidine and divide under crowded culture conditions, the "quiescent" cells continue to undergo changes, are metabolically active, and certainly do not grossly deteriorate.

摘要

本研究的目的是确定在长期静止期间,WI-38细胞是否会逐渐丢失不稳定成分,从而需要在受刺激的细胞进入G-1期并进入S期之前重新合成这些成分。当WI-38细胞进入并长时间维持在密度依赖性生长停滞状态时,对其代谢和分子状态进行了系统分析。我们的结果表明,WI-38细胞的生长停滞可分为两个阶段。第一个阶段,我们称之为“早期”生长停滞,发生在DNA合成和有丝分裂停止后的最初7-10天。与活跃增殖的细胞相比,其特征是生化变化很少。在早期生长停滞期间,细胞在血清刺激后不会出现复制前阶段的延长。相反,生长停滞10-20天的WI-38细胞在分子和生化水平上表现出许多变化(即总蛋白和总RNA含量降低两倍,大多数蛋白质水平降低,但纤连蛋白和胶原蛋白含量增加)。此外,在“后期”或“深度”生长停滞期间任何时间受到刺激的静止WI-38细胞确实会表现出延长的复制前阶段。尽管在十个代表性生长相关基因(即组蛋白H-3、p53、c-Ha-ras、2A9/钙周期蛋白、4F1/波形蛋白、低密度脂蛋白受体、胰岛素受体、胶原蛋白和纤连蛋白)的表达模式中也观察到了变化,但这些变化大多发生在细胞停止DNA合成和有丝分裂并进入静止状态时。当细胞维持在生长停滞状态时,所分析的生长相关转录本的稳态水平没有变化。因此,这些实验表明,尽管WI-38细胞在拥挤的培养条件下确实停止掺入胸苷并停止分裂,但“静止”细胞仍继续发生变化,具有代谢活性,并且肯定不会严重恶化。

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