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Cell Apoptosis and Autophagy in Renal Fibrosis.
Zhao, Xing-Chen; Livingston, Man J; Liang, Xin-Ling; Dong, Zheng.
  • Zhao XC; Division of Nephrology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
  • Livingston MJ; Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta University and Charlie Norwood VA Medical Center, Augusta, GA, 30912, USA.
  • Liang XL; Division of Nephrology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China. xinlingliang_ggh@163.com.
  • Dong Z; Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta University and Charlie Norwood VA Medical Center, Augusta, GA, 30912, USA. zdong@augusta.edu.
Adv Exp Med Biol ; 1165: 557-584, 2019.
Article en En | MEDLINE | ID: mdl-31399985
ABSTRACT
Renal fibrosis is the final common pathway of all chronic kidney diseases progressing to end-stage renal diseases. Autophagy, a highly conserved lysosomal degradation pathway, plays important roles in maintaining cellular homeostasis in all major types of kidney cells including renal tubular cells as well as podocytes, mesangial cells and endothelial cells in glomeruli. Autophagy dysfunction is implicated in the pathogenesis of various renal pathologies. Here, we analyze the pathological role and regulation of autophagy in renal fibrosis and related kidney diseases in both glomeruli and tubulointerstitial compartments. Further research is expected to gain significant mechanistic insights and discover pathway-specific and kidney-selective therapies targeting autophagy to prevent renal fibrosis and related kidney diseases.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Autofagia / Apoptosis / Riñón Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Autofagia / Apoptosis / Riñón Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article