黑腹果蝇心脏富集microrna随年龄性别特异性失调。

IF 5 2区 生物学 Q2 CELL BIOLOGY
Lijo N Varghese, Philip W Sheard, Daryl O Schwenke, Rajesh Katare
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引用次数: 0

摘要

心脏富集的microRNA (miRNA)表达失调与年龄相关的心血管疾病(cvd)有关。然而,发生失调的性别特异性和年龄仍不清楚。考虑到果蝇mirna的保守性和较短的寿命,我们研究了雄性和雌性果蝇心脏富集mirna (miR-1, -9, -34a, -133,靶mirna)表达的年龄相关变化及其对心管的影响。方法:从第7 ~ 70天,每隔7 d采集雄、雌蝇心管组织,每组5只。RT-qPCR检测mirna及靶基因(KCNQ、MRTF、SIRT2、CCN)表达情况(每组n=4 ~ 6)。通过马松三色染色(n=4-6)评估肌原纤维直径,以确定肥厚性miR-9的结构效应。结果:在女性中,miR-1随着年龄的增长而下调(p=),而在男性中,miR-9 (p=)和miR-34a (p= 0.0017)下调。有趣的是,miR-133在两性中均下调(p=。在男性中,MRTF(miR-9靶点)和CCN (miR-133靶点)的表达随年龄增加而增加(分别为p=0.016和p=0.013),而在女性中,KCNQ (miR-1靶点)和CCN的表达随年龄减少(分别为p=0.03和p=0.002)。在两性中,肌原纤维厚度随着年龄的增长而显著增加(p)。miR-9的下调可能在男性中促成了这种效应,而在女性中的机制尚不清楚。结论:这项研究为心脏衰老中性别特异性miRNA失调提供了新的见解,强调需要考虑miRNA介导的心血管衰老的性别差异,以及miRNA作为年龄相关心血管疾病诊断工具的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sex-specific dysregulation of cardiac-enriched microRNAs with age in Drosophila melanogaster.

Dysregulation of cardiac-enriched microRNA (miRNA) expression is linked to age-associated cardiovascular diseases (CVDs). However, the sex-specificity and age at which dysregulation occurs remain unclear. Given the conserved nature of miRNAs and short lifespan of Drosophila melanogaster (fruit flies), we investigated age-related changes in the expression of cardiac enriched miRNAs (miR-1, -9, -34a, and -133, target miRNAs) and their impact on the cardiac tube in male and female flies. Cardiac tube tissues were collected from male and female flies (n = 5/group) at 7-day intervals from day 7 to day 70. miRNAs and predicted target mRNA gene (KCNQ, MRTF, and CCN) expression were quantified by RT-qPCR (n = 4-6/group). Myofibril diameter was assessed by Masson's trichrome staining (n = 4-6) to determine the structural effects of hypertrophic miR-9. In females, miR-1 was downregulated with age (P ≤ 0.0001), whereas in males, miR-9 (P ≤ 0.0001) and miR-34a (P = 0.0017) were downregulated. Interestingly, miR-133 was downregulated in both sexes (P ≤ 0.0001). In males, MRTF (miR-9 target) and CCN (miR-133 target) expression increased with age (P = 0.016 and P = 0.013, respectively), whereas in females, KCNQ (miR-1 target) and CCN expression decreased (P = 0.03 and P = 0.002, respectively). Myofibril thickness significantly increased with age in both sexes (P < 0.0001). miR-9 downregulation may contribute to this effect in males, whereas the mechanism in females remains unclear. This study provides novel insights into sex-specific miRNA dysregulation in cardiac aging, emphasizing the need to consider sex differences in miRNA-mediated cardiovascular aging and the potential of miRNAs as diagnostic tools in age-related CVDs.NEW & NOTEWORTHY Advancements in healthcare and diet have increased life expectancy, doubling the population aged 60 and above by 2050. However, this longevity raises the risk of chronic diseases, especially cardiovascular diseases. We examined age-related changes in cardiovascular-enriched microRNAs in the Drosophila melanogaster heart. This first-of-its-kind observational study tracks microRNA changes across life stages. It highlights sex-specific expression of miRNAs, providing crucial insights into cardiac aging. It lays a strong foundation for future research on microRNA in heart health.

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来源期刊
CiteScore
9.10
自引率
1.80%
发文量
252
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Cell Physiology is dedicated to innovative approaches to the study of cell and molecular physiology. Contributions that use cellular and molecular approaches to shed light on mechanisms of physiological control at higher levels of organization also appear regularly. Manuscripts dealing with the structure and function of cell membranes, contractile systems, cellular organelles, and membrane channels, transporters, and pumps are encouraged. Studies dealing with integrated regulation of cellular function, including mechanisms of signal transduction, development, gene expression, cell-to-cell interactions, and the cell physiology of pathophysiological states, are also eagerly sought. Interdisciplinary studies that apply the approaches of biochemistry, biophysics, molecular biology, morphology, and immunology to the determination of new principles in cell physiology are especially welcome.
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