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The crosstalk between exosomes and ferroptosis: a review.
Wu, Jiao; Li, Zhongyu; Wu, Yu; Cui, Ning.
Afiliação
  • Wu J; Oncology Department of Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
  • Li Z; Department of Internal Medicine, Eye Hospital China Academy of Chinese Medical Sciences, Beijing, China. lzy681bj@163.com.
  • Wu Y; Oncology Department of Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China. wy713vip@163.com.
  • Cui N; Oncology Department of Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Cell Death Discov ; 10(1): 170, 2024 Apr 09.
Article em En | MEDLINE | ID: mdl-38594265
ABSTRACT
Exosomes are a subtype of extracellular vesicles composed of bioactive molecules, including nucleic acids, proteins, and lipids. Exosomes are generated by the fusion of intracellular multivesicular bodies (MVBs) with the cell membrane and subsequently released into the extracellular space to participate in intercellular communication and diverse biological processes within target cells. As a crucial mediator, exosomes have been implicated in regulating ferroptosis-an iron-dependent programmed cell death characterized by lipid peroxide accumulation induced by reactive oxygen species. The involvement of exosomes in iron, lipid, and amino acid metabolism contributes to their regulatory role in specific mechanisms underlying how exosomes modulate ferroptosis, which remains incompletely understood, and some related studies are still preliminary. Therefore, targeting the regulation of ferroptosis by exosomes holds promise for future clinical treatment strategies across various diseases. This review aims to provide insights into the pathophysiology and mechanisms governing the interaction between exosomes and ferroptosis and their implications in disease development and treatment to serve as a reference for further research.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cell Death Discov Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cell Death Discov Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China
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