Your browser doesn't support javascript.
loading
Golgi defect as a major contributor to lysosomal dysfunction.
Akaaboune, Sarah R; Wang, Yanzhuang.
Afiliación
  • Akaaboune SR; Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
  • Wang Y; Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, MI, United States.
Front Cell Dev Biol ; 12: 1386149, 2024.
Article en En | MEDLINE | ID: mdl-38721528
ABSTRACT
The Golgi apparatus plays a crucial role in lysosome biogenesis and the delivery of lysosomal enzymes, essential for maintaining cellular homeostasis and ensuring cell survival. Deficiencies in Golgi structure and function can profoundly impact lysosomal homeostasis, leading to various lysosomal storage diseases and neurodegenerative disorders. In this review, we highlight the role of the Golgi Reassembly Stacking Proteins (GRASPs) in the formation and function of the Golgi apparatus, emphasizing the current understanding of the association between the Golgi apparatus, lysosomes, and lysosomal storage diseases. Additionally, we discuss how Golgi dysfunction leads to the secretion of lysosomal enzymes. This review aims to serve as a concise resource, offering insights into Golgi structure, function, disease-related defects, and their consequential effects on lysosomal biogenesis and function. By highlighting Golgi defects as an underappreciated contributor to lysosomal dysfunction across various diseases, we aim to enhance comprehension of these intricate cellular processes.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Dev Biol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Suiza