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首页> 外文期刊>Journal of cardiovascular translational research >The role of sex differences in autophagy in the heart during coxsackievirus B3-induced myocarditis
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The role of sex differences in autophagy in the heart during coxsackievirus B3-induced myocarditis

机译:柯萨奇病毒B3诱导的心肌炎中性别差异在心脏自噬中的作用

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摘要

Under normal conditions, autophagy maintains cardiomyocyte health and integrity through turnover of organelles. During stress, oxygen and nutrient deprivation, or microbial infection, autophagy prolongs cardiomyocyte survival. Sex differences in induction of cell death may to some extent explain the disparity between the sexes in many human diseases. However, sex differences in gene expression, which regulate cell death and autophagy, were so far not taken in consideration to explain the sex bias of viral myocarditis. Coxsackievirus B3 (CVB3)-induced myocarditis is a sex-biased disease, with females being substantially less susceptible than males and sex hormones largely determine this bias. CVB3 was shown to induce and subvert the autophagosome for its optimal viral RNA replication. Gene expression analysis on mouse and human, healthy and CVB3-infected, cardiac samples of both sexes, suggests sex differences in autophagy-related gene expression. This review discusses the aspects of sex bias in autophagy induction in cardiomyocytes.
机译:在正常情况下,自噬通过细胞器的更新来维持心肌细胞的健康和完整性。在应激、缺氧和营养或微生物感染期间,自噬会延长心肌细胞的存活时间。诱导细胞死亡的性别差异可能在一定程度上解释了许多人类疾病中性别之间的差异。然而,迄今为止,调节细胞死亡和自噬的基因表达的性别差异尚未被考虑在解释病毒性心肌炎的性别偏倚中。柯萨奇病毒 B3 (CVB3) 诱导的心肌炎是一种性别偏倚性疾病,女性的易感性远低于男性,性激素在很大程度上决定了这种偏倚。CVB3 被证明可以诱导和破坏自噬体,以实现其最佳的病毒 RNA 复制。对小鼠和人类、健康和 CVB3 感染的心脏样本进行基因表达分析,表明自噬相关基因表达存在性别差异。本文将讨论心肌细胞自噬诱导中的性别偏倚。

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