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The host mannose-6-phosphate pathway and viral infection.
Liu, Qincheng; Wang, Weiqi; Xu, Liwei; Zhang, Qisheng; Wang, Hongna.
Afiliação
  • Liu Q; Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.
  • Wang W; Key Laboratory for Cell Homeostasis and Cancer Research of Guangdong Higher Education Institutes, Guangzhou, China.
  • Xu L; Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.
  • Zhang Q; Key Laboratory for Cell Homeostasis and Cancer Research of Guangdong Higher Education Institutes, Guangzhou, China.
  • Wang H; Affiliated Cancer Hospital & Institute of Guangzhou Medical University, Guangzhou, China.
Front Cell Infect Microbiol ; 14: 1349221, 2024.
Article em En | MEDLINE | ID: mdl-38357444
ABSTRACT
Viruses, despite their simple structural composition, engage in intricate and complex interactions with their hosts due to their parasitic nature. A notable demonstration of viral behavior lies in their exploitation of lysosomes, specialized organelles responsible for the breakdown of biomolecules and clearance of foreign substances, to bolster their own replication. The man-nose-6-phosphate (M6P) pathway, crucial for facilitating the proper transport of hydrolases into lysosomes and promoting lysosome maturation, is frequently exploited for viral manipulation in support of replication. Recently, the discovery of lysosomal enzyme trafficking factor (LYSET) as a pivotal regulator within the lysosomal M6P pathway has introduced a fresh perspective on the intricate interplay between viral entry and host factors. This groundbreaking revelation illuminates unexplored dimensions of these interactions. In this review, we endeavor to provide a thorough overview of the M6P pathway and its intricate interplay with viral factors during infection. By consolidating the current understanding in this field, our objective is to establish a valuable reference for the development of antiviral drugs that selectively target the M6P pathway.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Viroses / Hidrolases Limite: Humans Idioma: En Revista: Front Cell Infect Microbiol / Front. cell. infect. microbiol / Frontiers in cellular and infection microbiology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Viroses / Hidrolases Limite: Humans Idioma: En Revista: Front Cell Infect Microbiol / Front. cell. infect. microbiol / Frontiers in cellular and infection microbiology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China
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