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细胞过度生长导致细胞质稀释,并导致衰老。

Excessive Cell Growth Causes Cytoplasm Dilution And Contributes to Senescence.

机构信息

David H. Koch Institute for Integrative Cancer Research, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

David H. Koch Institute for Integrative Cancer Research, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA; Department of Systems Biology, Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cell. 2019 Feb 21;176(5):1083-1097.e18. doi: 10.1016/j.cell.2019.01.018. Epub 2019 Feb 7.

Abstract

Cell size varies greatly between cell types, yet within a specific cell type and growth condition, cell size is narrowly distributed. Why maintenance of a cell-type specific cell size is important remains poorly understood. Here we show that growing budding yeast and primary mammalian cells beyond a certain size impairs gene induction, cell-cycle progression, and cell signaling. These defects are due to the inability of large cells to scale nucleic acid and protein biosynthesis in accordance with cell volume increase, which effectively leads to cytoplasm dilution. We further show that loss of scaling beyond a certain critical size is due to DNA becoming limiting. Based on the observation that senescent cells are large and exhibit many of the phenotypes of large cells, we propose that the range of DNA:cytoplasm ratio that supports optimal cell function is limited and that ratios outside these bounds contribute to aging.

摘要

细胞大小在不同细胞类型之间差异很大,但在特定的细胞类型和生长条件下,细胞大小分布狭窄。为什么维持特定细胞类型的细胞大小很重要,目前仍知之甚少。在这里,我们表明,酵母出芽和哺乳动物原代细胞生长到一定大小后,会损害基因诱导、细胞周期进程和细胞信号转导。这些缺陷是由于大细胞无法根据细胞体积的增加来调整核酸和蛋白质生物合成,这实际上导致了细胞质稀释。我们进一步表明,超过一定临界大小的缩放丢失是由于 DNA 变得有限。基于衰老细胞体积较大并表现出许多大细胞表型的观察结果,我们提出支持最佳细胞功能的 DNA:细胞质比的范围是有限的,并且超出这些范围的比值会导致衰老。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d07/6386581/21b75f19cb95/fx1.jpg

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