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在没有外部应激源的情况下细菌的衰老。

Bacterial ageing in the absence of external stressors.

机构信息

Biosciences, University of Exeter, Exeter, Devon EX4 4QD, UK.

Living Systems Institute, University of Exeter, Exeter, Devon EX4 4QD, UK.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2019 Nov 25;374(1786):20180442. doi: 10.1098/rstb.2018.0442. Epub 2019 Oct 7.

Abstract

Evidence of ageing in the bacterium was a landmark finding in senescence research, as it suggested that even organisms with morphologically symmetrical fission may have evolved strategies to permit damage accumulation. However, recent work has suggested that ageing is only detectable in this organism in the presence of extrinsic stressors, such as the fluorescent proteins and strong light sources typically used to excite them. Here we combine microfluidics with brightfield microscopy to provide evidence of ageing in in the absence of these stressors. We report (i) that the doubling time of the lineage of cells that consistently inherits the 'maternal old pole' progressively increases with successive rounds of cell division until it reaches an apparent asymptote, and (ii) that the parental cell divides asymmetrically, with the old pole daughter showing a longer doubling time and slower glucose accumulation than the new pole daughter. Notably, these patterns arise without the progressive accumulation or asymmetric partitioning of observable misfolded-protein aggregates, phenomena previously hypothesized to cause the ageing phenotype. Our findings suggest that ageing is part of the naturally occurring ecologically-relevant phenotype of this bacterium and highlight the importance of alternative mechanisms of damage accumulation in this context. This article is part of a discussion meeting issue 'Single cell ecology'.

摘要

衰老在细菌中的证据是衰老研究中的一个里程碑式发现,因为它表明,即使是形态上具有对称分裂的生物体,也可能已经进化出了允许损伤积累的策略。然而,最近的研究表明,只有在存在外在应激源的情况下,这种生物体才会出现衰老迹象,例如通常用于激发它们的荧光蛋白和强光源。在这里,我们结合微流控技术和明场显微镜,在没有这些应激源的情况下提供了衰老的证据。我们报告(i)在连续几代细胞中,始终继承“母体老极”的细胞系的倍增时间随着细胞分裂的连续进行而逐渐增加,直到达到明显的渐近线,以及(ii)亲代细胞不对称分裂,老极子细胞的倍增时间比新极子细胞长,葡萄糖积累速度也较慢。值得注意的是,这些模式的出现并没有可观察到的错误折叠蛋白聚集体的累积或不对称分配,这些现象以前被假设为导致衰老表型的原因。我们的发现表明,衰老是这种细菌自然发生的生态相关表型的一部分,并强调了在这种情况下损伤积累的替代机制的重要性。本文是一次关于“单细胞生态学”的讨论会议的一部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6c69/6792439/7a34e08d3024/rstb20180442-g1.jpg

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