Ambra1 in exosomes secreted by HK-2 cells damaged by supersaturated oxalate induce mitophagy and autophagy-ferroptosis in normal HK-2 cells to participate in the occurrence of kidney stones.


Journal

Biochimica et biophysica acta. Molecular cell research
ISSN: 1879-2596
Titre abrégé: Biochim Biophys Acta Mol Cell Res
Pays: Netherlands
ID NLM: 101731731

Informations de publication

Date de publication:
01 2024
Historique:
received: 24 04 2023
revised: 23 09 2023
accepted: 27 09 2023
medline: 20 11 2023
pubmed: 9 10 2023
entrez: 8 10 2023
Statut: ppublish

Résumé

Injury to the renal tubular epithelium has emerged as a leading factor underlying the formation of kidney stones. Indeed, epithelial cell damage contributes to the adherence and aggregation of crystals, thereby accelerating the formation of renal stones. Meanwhile, exosomes play an instrumental role in cellular communication, including DNA, RNA, mRNA, etc. In this study, homogenous cells were treated with exosomes derived from damaged cells in an attempt to establish "positive feedback" of cell damage, and the desired results were achieved. To begin, a serum-free medium and supersaturated concentrations of oxalate were added to the HK-2 cell line, and then exosomes were isolated from the two groups for analysis and comparison, and the autophagy-related gene Ambra1 (autophagy and beclin-1 regulator 1) was detected. Subsequently, normal HK-2 cells were treated with exosomes, and the related indexes of autophagy, ferroptosis and mitophagy were determined. Thereafter, Ambra1 was knocked down in exosome-derived HK-2 cells, resulting in the down-regulation of Ambra1 expression in exosomes produced by HK-2 cells following oxalate intervention. Thereafter, the ability of exosomes to stimulate autophagy, mitophagy and ferroptosis was re-evaluated in HK-2 cells after Ambra1 knockdown. The results corroborated that exosomes secreted by oxalate-treated HK-2 can directly elevate autophagy, ferroptosis and mitophagy levels in normal cells, and this effect was significantly mitigated following Ambra1 knockdown within exosomes. Meanwhile, exosomes-induced autophagy and ferroptosis were alleviated after knockdown of beclin-1 in recipient HK-2 cells. These results further suggest that beclin-1 plays a critical role in the process of exosome-induced autophagy-ferroptosis.

Identifiants

pubmed: 37806389
pii: S0167-4889(23)00177-5
doi: 10.1016/j.bbamcr.2023.119604
pii:
doi:

Substances chimiques

Beclin-1 0
Oxalates 0
AMBRA1 protein, human 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

119604

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Sixing Yang reports financial support was provided by National Natural Science Foundation of China. Wenbiao Liao reports financial support was provided by National Natural Science Foundation of Hubei Province.

Auteurs

Xiaozhe Su (X)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Chao Song (C)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Ziqi He (Z)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Qianlin Song (Q)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Lingchao Meng (L)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Caitao Dong (C)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Jiawei Zhou (J)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Hu Ke (H)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Yunhe Xiong (Y)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Junwei Liu (J)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China.

Wenbiao Liao (W)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China. Electronic address: liaowenbiao@whu.edu.cn.

Sixing Yang (S)

Department of Urology, Renmin Hospital of Wuhan University, Wuhan, China. Electronic address: sxyang@whu.edu.cn.

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Classifications MeSH