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急性运动导致免疫细胞中端粒相关基因和微小RNA表达的调节。

Acute exercise leads to regulation of telomere-associated genes and microRNA expression in immune cells.

作者信息

Chilton Warrick L, Marques Francine Z, West Jenny, Kannourakis George, Berzins Stuart P, O'Brien Brendan J, Charchar Fadi J

机构信息

School of Health Sciences, Federation University Australia, Victoria, Australia.

Fiona Elsey Cancer Research Institute, Ballarat, Victoria, Australia.

出版信息

PLoS One. 2014 Apr 21;9(4):e92088. doi: 10.1371/journal.pone.0092088. eCollection 2014.

Abstract

Telomeres are specialized nucleoprotein structures that protect chromosomal ends from degradation. These structures progressively shorten during cellular division and can signal replicative senescence below a critical length. Telomere length is predominantly maintained by the enzyme telomerase. Significant decreases in telomere length and telomerase activity are associated with a host of chronic diseases; conversely their maintenance underpins the optimal function of the adaptive immune system. Habitual physical activity is associated with longer leukocyte telomere length; however, the precise mechanisms are unclear. Potential hypotheses include regulation of telomeric gene transcription and/or microRNAs (miRNAs). We investigated the acute exercise-induced response of telomeric genes and miRNAs in twenty-two healthy males (mean age = 24.1±1.55 years). Participants undertook 30 minutes of treadmill running at 80% of peak oxygen uptake. Blood samples were taken before exercise, immediately post-exercise and 60 minutes post-exercise. Total RNA from white blood cells was submitted to miRNA arrays and telomere extension mRNA array. Results were individually validated in white blood cells and sorted T cell lymphocyte subsets using quantitative real-time PCR (qPCR). Telomerase reverse transcriptase (TERT) mRNA (P = 0.001) and sirtuin-6 (SIRT6) (P<0.05) mRNA expression were upregulated in white blood cells after exercise. Fifty-six miRNAs were also differentially regulated post-exercise (FDR <0.05). In silico analysis identified four miRNAs (miR-186, miR-181, miR-15a and miR-96) that potentially targeted telomeric gene mRNA. The four miRNAs exhibited significant upregulation 60 minutes post-exercise (P<0.001). Telomeric repeat binding factor 2, interacting protein (TERF2IP) was identified as a potential binding target for miR-186 and miR-96 and demonstrated concomitant downregulation (P<0.01) at the corresponding time point. Intense cardiorespiratory exercise was sufficient to differentially regulate key telomeric genes and miRNAs in white blood cells. These results may provide a mechanistic insight into telomere homeostasis and improved immune function and physical health.

摘要

端粒是一种特殊的核蛋白结构,可保护染色体末端不被降解。这些结构在细胞分裂过程中会逐渐缩短,当长度低于临界值时会发出复制衰老信号。端粒长度主要由端粒酶维持。端粒长度和端粒酶活性的显著降低与许多慢性疾病有关;相反,它们的维持是适应性免疫系统最佳功能的基础。习惯性体育活动与更长的白细胞端粒长度有关;然而,确切机制尚不清楚。潜在的假说是端粒基因转录和/或微小RNA(miRNA)的调控。我们研究了22名健康男性(平均年龄=24.1±1.55岁)端粒基因和miRNA的急性运动诱导反应。参与者在最大摄氧量的80%下进行30分钟的跑步机跑步。在运动前、运动后立即和运动后60分钟采集血样。从白细胞中提取的总RNA被用于miRNA芯片和端粒延伸mRNA芯片。结果在白细胞和分选的T细胞淋巴细胞亚群中使用定量实时PCR(qPCR)进行了单独验证。运动后白细胞中端粒酶逆转录酶(TERT)mRNA(P=0.001)和沉默调节蛋白6(SIRT6)(P<0.05)mRNA表达上调。运动后还有56种miRNA受到差异调节(FDR<0.05)。计算机分析确定了四种可能靶向端粒基因mRNA的miRNA(miR-186、miR-181、miR-15a和miR-96)。这四种miRNA在运动后60分钟表现出显著上调(P<0.001)。端粒重复结合因子2相互作用蛋白(TERF2IP)被确定为miR-186和miR-96的潜在结合靶点,并在相应时间点表现出伴随性下调(P<0.01)。剧烈的心肺运动足以差异调节白细胞中的关键端粒基因和miRNA。这些结果可能为端粒稳态以及改善免疫功能和身体健康提供机制上的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e0f/3994003/440d9910aeaa/pone.0092088.g001.jpg

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