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lamin B1 的下降是与年龄相关的成年海马神经发生丧失的基础。

Lamin B1 decline underlies age-related loss of adult hippocampal neurogenesis.

机构信息

Laboratory of Genetics, The Salk Institute for Biological Studies, La Jolla, CA, USA.

Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH, USA.

出版信息

EMBO J. 2021 Feb 1;40(3):e105819. doi: 10.15252/embj.2020105819. Epub 2020 Dec 10.

Abstract

Neurogenesis in the adult hippocampus declines with age, a process that has been implicated in cognitive and emotional impairments. However, the mechanisms underlying this decline have remained elusive. Here, we show that the age-dependent downregulation of lamin B1, one of the nuclear lamins in adult neural stem/progenitor cells (ANSPCs), underlies age-related alterations in adult hippocampal neurogenesis. Our results indicate that higher levels of lamin B1 in ANSPCs safeguard against premature differentiation and regulate the maintenance of ANSPCs. However, the level of lamin B1 in ANSPCs declines during aging. Precocious loss of lamin B1 in ANSPCs transiently promotes neurogenesis but eventually depletes it. Furthermore, the reduction of lamin B1 in ANSPCs recapitulates age-related anxiety-like behavior in mice. Our results indicate that the decline in lamin B1 underlies stem cell aging and impacts the homeostasis of adult neurogenesis and mood regulation.

摘要

成年海马体中的神经发生随着年龄的增长而下降,这一过程与认知和情感障碍有关。然而,这种下降的机制仍然难以捉摸。在这里,我们表明,核纤层蛋白 B1(成年神经干细胞/祖细胞(ANSPCs)中的一种核纤层蛋白)的年龄依赖性下调是成年海马体神经发生与年龄相关变化的基础。我们的结果表明,ANSPCs 中更高水平的核纤层蛋白 B1可防止过早分化,并调节 ANSPCs 的维持。然而,ANSPCs 中的核纤层蛋白 B1水平在衰老过程中下降。ANSPCs 中核纤层蛋白 B1 的过早缺失会短暂促进神经发生,但最终会耗尽它。此外,ANSPCs 中核纤层蛋白 B1 的减少会在小鼠中再现与年龄相关的焦虑样行为。我们的结果表明,核纤层蛋白 B1 的下降是干细胞衰老的基础,并影响成年神经发生和情绪调节的动态平衡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b83/7849303/e201c96cdf43/EMBJ-40-e105819-g002.jpg

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