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单细胞 RNA 测序检测与年龄相关的基因,这些基因可鉴定老年小鼠肝脏中的衰老细胞。

Single-cell RNA sequencing to detect age-associated genes that identify senescent cells in the liver of aged mice.

机构信息

Molecular Regulation of Aging, Tokyo Metropolitan Institute for Geriatrics and Gerontology, 35-2 Sakae-cho, Itabashi-ku, Tokyo, 173-0015, Japan.

Department of Biological Sciences, Tokyo Metropolitan University, Tokyo, 192-0397, Japan.

出版信息

Sci Rep. 2023 Aug 30;13(1):14186. doi: 10.1038/s41598-023-41352-6.

Abstract

Senescent cells are predicted to occur and increase in animal tissues with aging. However, senescent cells in the tissues of aged animals remain to be identified. We refer to the marker genes to identify senescent cells in tissues as "age-associated genes". In this study, we searched for age-associated genes to identify senescent cells in the livers of aged animals. We performed single-cell RNA sequencing (scRNA-seq) to screen candidates for age-associated genes using young and aged rat primary hepatocytes. To remove animal species specificity, gene expression analyses in mouse livers were performed, confirming age-associated increases in the mRNA expression levels of Glipr1, Clec12a, and Phlda3. Moreover, the mRNA expression levels of Glipr1 and Phlda3 were increased by stress-induced premature senescence using doxorubicin in primary hepatocytes and livers of young mice. Transcriptome data of aged rat hepatocytes suggested that Glipr1, Clec12a, and Phlda3 were expressed in almost identical cells. Fluorescence in situ hybridization (FISH) confirmed the presence of cells with abundant Glipr1, Clec12a, and Phlda3 mRNA in 27-month-old mouse primary hepatocytes, which are considered to be senescent cells. This study is the first to identify Glipr1, Clec12a, and Phlda3 as age-associated genes in the mouse liver.

摘要

衰老细胞预计会在动物组织中随着衰老而出现和增加。然而,衰老动物组织中的衰老细胞仍有待鉴定。我们将鉴定组织中衰老细胞的标记基因称为“与年龄相关的基因”。在这项研究中,我们搜索了与年龄相关的基因,以鉴定老年动物肝脏中的衰老细胞。我们对年轻和老年大鼠原代肝细胞进行了单细胞 RNA 测序 (scRNA-seq),以筛选候选的与年龄相关的基因。为了去除动物种属特异性,我们在小鼠肝脏中进行了基因表达分析,证实了 Glipr1、Clec12a 和 Phlda3 的 mRNA 表达水平随年龄增长而增加。此外,在原代肝细胞和年轻小鼠肝脏中,用多柔比星诱导应激性早衰,Glipr1 和 Phlda3 的 mRNA 表达水平也增加了。老年大鼠肝细胞的转录组数据表明,Glipr1、Clec12a 和 Phlda3 在几乎相同的细胞中表达。荧光原位杂交 (FISH) 证实了在 27 月龄的小鼠原代肝细胞中存在大量 Glipr1、Clec12a 和 Phlda3 mRNA 的细胞,这些细胞被认为是衰老细胞。这项研究首次鉴定出 Glipr1、Clec12a 和 Phlda3 是小鼠肝脏中的与年龄相关的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/28e8/10468526/5c0e3911416d/41598_2023_41352_Fig1_HTML.jpg

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