The Role of MicroRNAs in Proteostasis Decline and Protein Aggregation during Brain and Skeletal Muscle Aging

被引:8
|
作者
Francisco, Stephany [1 ]
Martinho, Vera [1 ]
Ferreira, Margarida [1 ]
Reis, Andreia [1 ]
Moura, Gabriela [1 ]
Soares, Ana Raquel [1 ]
Santos, Manuel A. S. [1 ,2 ]
机构
[1] Univ Aveiro, Inst Biomed iBiMED, Dept Med Sci, P-3810193 Aveiro, Portugal
[2] Univ Coimbra, Fac Med, Multidisciplinary Inst Aging, MIA Portugal, Rua Largo 2,3, P-3000370 Coimbra, Portugal
关键词
miRNA; mammalian tissue aging; age-related protein aggregation; proteostasis network; HEAT-SHOCK RESPONSE; AUTOPHAGY IMPAIRMENT; UBIQUITIN LIGASES; MIRNA BIOGENESIS; ER STRESS; EXPRESSION; TARGET; DROSHA; DEGRADATION; MURF1;
D O I
10.3390/ijms23063232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aging can be defined as the progressive deterioration of cellular, tissue, and organismal function over time. Alterations in protein homeostasis, also known as proteostasis, are a hallmark of aging that lead to proteome imbalances and protein aggregation, phenomena that also occur in age-related diseases. Among the various proteostasis regulators, microRNAs (miRNAs) have been reported to play important roles in the post-transcriptional control of genes involved in maintaining proteostasis during the lifespan in several organismal tissues. In this review, we consolidate recently published reports that demonstrate how miRNAs regulate fundamental proteostasis-related processes relevant to tissue aging, with emphasis on the two most studied tissues, brain tissue and skeletal muscle. We also explore an emerging perspective on the role of miRNA regulatory networks in age-related protein aggregation, a known hallmark of aging and age-related diseases, to elucidate potential miRNA candidates for anti-aging diagnostic and therapeutic targets.
引用
收藏
页数:17
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