Aggrephagy Deficiency in the Placenta: A New Pathogenesis of Preeclampsia.

Aggrephagy Deficiency in the Placenta: A New Pathogenesis of Preeclampsia.
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DOI:
10.3390/ijms22052432
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发表时间:
2021-02-28
影响因子:
5.6
通讯作者:
Saito S
Saito S
中科院分区:
生物学2区
文献类型:
--
作者:
Nakashima A;Shima T;Tsuda S;Aoki A;Kawaguchi M;Furuta A;Yasuda I;Yoneda S;Yamaki-Ushijima A;Cheng SB;Sharma S;Saito S

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Aggrephagy is defined as the selective degradation of aggregated proteins by autophagosomes. Protein aggregation in organs and cells has been highlighted as a cause of multiple diseases, including neurodegenerative diseases, cardiac failure, and renal failure. Aggregates could pose a hazard for cell survival. Cells exhibit three main mechanisms against the accumulation of aggregates: protein refolding by upregulation of chaperones, reduction of protein overload by translational inhibition, and protein degradation by the ubiquitin–proteasome and autophagy–lysosome systems. Deletion of autophagy-related genes reportedly contributes to intracellular protein aggregation in vivo. Some proteins recognized in aggregates in preeclamptic placentas include those involved in neurodegenerative diseases. As aggregates are derived both intracellularly and extracellularly, special endocytosis for extracellular aggregates also employs the autophagy machinery. In this review, we discuss how the deficiency of aggrephagy and/or macroautophagy leads to poor placentation, resulting in preeclampsia or fetal growth restriction.
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