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哺乳动物细胞大小的控制与维持。

Control and maintenance of mammalian cell size.

作者信息

Cooper Stephen

机构信息

Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109-0620, USA.

出版信息

BMC Cell Biol. 2004 Sep 29;5(1):35. doi: 10.1186/1471-2121-5-35.

Abstract

BACKGROUND

Conlon and Raff propose that mammalian cells grow linearly during the division cycle. According to Conlon and Raff, cells growing linearly do not need a size checkpoint to maintain a constant distribution of cell sizes. If there is no cell-size-control system, then exponential growth is not allowed, as exponential growth, according to Conlon and Raff, would require a cell-size-control system.

DISCUSSION

A reexamination of the model and experiments of Conlon and Raff indicates that exponential growth is fully compatible with cell size maintenance, and that mammalian cells have a system to regulate and maintain cell size that is related to the process of S-phase initiation. Mammalian cell size control and its relationship to growth rate-faster growing cells are larger than slower growing cells-is explained by the initiation of S phase occurring at a relatively constant cell size coupled with relatively invariant S- and G2-phase times as interdivision time varies.

SUMMARY

This view of the mammalian cell cycle, the continuum model, explains the mass growth pattern during the division cycle, size maintenance, size determination, and the kinetics of cell-size change following a shift-up from slow to rapid growth.

摘要

背景

康伦和拉夫提出,哺乳动物细胞在分裂周期中呈线性生长。根据康伦和拉夫的观点,线性生长的细胞不需要大小检查点来维持细胞大小的恒定分布。如果没有细胞大小控制系统,那么指数生长就不被允许,因为根据康伦和拉夫的观点,指数生长需要一个细胞大小控制系统。

讨论

对康伦和拉夫的模型及实验的重新审视表明,指数生长与细胞大小维持完全兼容,并且哺乳动物细胞具有一个与S期起始过程相关的调节和维持细胞大小的系统。哺乳动物细胞大小控制及其与生长速率的关系——生长较快的细胞比生长较慢的细胞大——可以通过在相对恒定的细胞大小下发生S期起始来解释,随着分裂间期的变化,S期和G2期时间相对不变。

总结

这种关于哺乳动物细胞周期的观点,即连续模型,解释了分裂周期中的质量生长模式、大小维持、大小确定以及从缓慢生长转变为快速生长后细胞大小变化的动力学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5f5/524481/0ccce22933e1/1471-2121-5-35-9.jpg

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