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比较百岁老人和中年女性淋巴母细胞系的 RNA 测序,确定了与年龄相关的硒蛋白、热休克蛋白、CD99 和 BID 基因表达失调。

RNA sequencing comparing centenarian and middle-aged women lymphoblastoid cell lines identifies age-related dysregulated expression of genes encoding selenoproteins, heat shock proteins, CD99, and BID.

机构信息

Department of Human Molecular Genetics and Biochemistry, Faculty of Health and Medical Sciences, Tel Aviv University, Tel Aviv, 69978, Israel.

Department of Cell and Developmental Biology, Faculty of Health and Medical Sciences, Tel Aviv University, Tel Aviv, 69978, Israel.

出版信息

Drug Dev Res. 2024 Nov;85(7):e70011. doi: 10.1002/ddr.70011.

Abstract

Women typically live longer than men, and constitute the majority of centenarians. We applied RNA-sequencing (RNA-seq) of blood-derived lymphoblastoid cell lines (LCLs) from women aged 60-80 years and centenarians (100-105 years), validated the RNA-seq findings by real-time PCR, and additionally measured the differentially expressed genes in LCLs from young women aged 20-35 years. Top RNA-seq genes with differential expression between the age groups included three selenoproteins (GPX1, SELENOW, SELENOH) and three heat shock proteins (HSPA6, HSPA1A, HSPA1B), with the highest expression in LCLs from young women, indicating that young women are better protected from oxidative stress. The expression of two additional genes, BID encoding BH3-interacting domain death agonist and CD99 encoding CD99 antigen, showed unique age dependence, with similar expression levels in young and centenarian women while exhibiting higher and lower expression levels, respectively, in LCLs from women aged 60-80 years compared with the two other age groups. This age-related differential expression of BID and CD99 suggests elevated inflammation susceptibility in middle-aged women compared with either young or centenarian women. Our findings, once validated with human peripheral blood mononuclear cells and further cell types, may lead to novel healthy aging diagnostics and therapeutics.

摘要

女性的寿命通常比男性长,并且在百岁老人中占多数。我们对年龄在 60-80 岁的女性和百岁老人(100-105 岁)的血液衍生淋巴母细胞系(LCL)进行了 RNA 测序(RNA-seq),通过实时 PCR 验证了 RNA-seq 结果,并在年轻女性(20-35 岁)的 LCL 中测量了差异表达的基因。年龄组之间差异表达的顶级 RNA-seq 基因包括三个硒蛋白(GPX1、SELENOW、SELENOH)和三个热休克蛋白(HSPA6、HSPA1A、HSPA1B),在年轻女性的 LCL 中表达最高,表明年轻女性受到氧化应激的保护更好。另外两个基因 BID(编码 BH3 相互作用域死亡激动剂)和 CD99(编码 CD99 抗原)的表达表现出独特的年龄依赖性,在年轻女性和百岁老人女性中的表达水平相似,而在年龄在 60-80 岁的女性的 LCL 中的表达水平分别更高和更低。BID 和 CD99 的这种年龄相关差异表达表明,与年轻或百岁老人女性相比,中年女性的炎症易感性增加。我们的发现,一旦用人外周血单核细胞和进一步的细胞类型进行验证,可能会导致新的健康衰老诊断和治疗方法。

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