Literature DB >> 32704047

Autophagy in kidney homeostasis and disease.

Chengyuan Tang1, Man J Livingston2, Zhiwen Liu1, Zheng Dong3,4,5.   

Abstract

Autophagy is a conserved lysosomal pathway for the degradation of cytoplasmic components. Basal autophagy in kidney cells is essential for the maintenance of kidney homeostasis, structure and function. Under stress conditions, autophagy is altered as part of the adaptive response of kidney cells, in a process that is tightly regulated by signalling pathways that can modulate the cellular autophagic flux - mammalian target of rapamycin, AMP-activated protein kinase and sirtuins are key regulators of autophagy. Dysregulated autophagy contributes to the pathogenesis of acute kidney injury, to incomplete kidney repair after acute kidney injury and to chronic kidney disease of varied aetiologies, including diabetic kidney disease, focal segmental glomerulosclerosis and polycystic kidney disease. Autophagy also has a role in kidney ageing. However, questions remain about whether autophagy has a protective or a pathological role in kidney fibrosis, and about the precise mechanisms and signalling pathways underlying the autophagy response in different types of kidney cells and across the spectrum of kidney diseases. Further research is needed to gain insights into the regulation of autophagy in the kidneys and to enable the discovery of pathway-specific and kidney-selective therapies for kidney diseases and anti-ageing strategies.

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Year:  2020        PMID: 32704047     DOI: 10.1038/s41581-020-0309-2

Source DB:  PubMed          Journal:  Nat Rev Nephrol        ISSN: 1759-5061            Impact factor:   28.314


  69 in total

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Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 2.622

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Journal:  Pharmacol Res       Date:  2021-12-09       Impact factor: 7.658

Review 4.  Emerging role of tumor suppressor p53 in acute and chronic kidney diseases.

Authors:  Jessica M Overstreet; Cody C Gifford; Jiaqi Tang; Paul J Higgins; Rohan Samarakoon
Journal:  Cell Mol Life Sci       Date:  2022-08-09       Impact factor: 9.207

5.  AMP-activated protein kinase contributes to cisplatin-induced renal epithelial cell apoptosis and acute kidney injury.

Authors:  Xiaogao Jin; Changlong An; Baihai Jiao; Robert L Safirstein; Yanlin Wang
Journal:  Am J Physiol Renal Physiol       Date:  2020-10-26

6.  PARK7 Protects Against Chronic Kidney Injury and Renal Fibrosis by Inducing SOD2 to Reduce Oxidative Stress.

Authors:  Lijun Yin; Honglin Li; Zhiwen Liu; Wenwen Wu; Juan Cai; Chengyuan Tang; Zheng Dong
Journal:  Front Immunol       Date:  2021-05-21       Impact factor: 7.561

7.  IFT88 deficiency in proximal tubular cells exaggerates cisplatin-induced injury by suppressing autophagy.

Authors:  Shixuan Wang; Shougang Zhuang; Zheng Dong
Journal:  Am J Physiol Renal Physiol       Date:  2021-07-12

Review 8.  Mesenchymal Stem Cell-Derived Extracellular Vesicles: A Potential Therapeutic Strategy for Acute Kidney Injury.

Authors:  Jia-Kun Li; Cheng Yang; Ying Su; Jing-Chao Luo; Ming-Hao Luo; Dan-Lei Huang; Guo-Wei Tu; Zhe Luo
Journal:  Front Immunol       Date:  2021-06-03       Impact factor: 8.786

9.  Epidermal Growth Factor Protects Against High Glucose-Induced Podocyte Injury Possibly via Modulation of Autophagy and PI3K/AKT/mTOR Signaling Pathway Through DNA Methylation.

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10.  Sirt3 promotes the autophagy of HK‑2 human proximal tubular epithelial cells via the inhibition of Notch‑1/Hes‑1 signaling.

Authors:  Ying Wang; Jiang Chang; Zi-Qiang Wang; Ying Li
Journal:  Mol Med Rep       Date:  2021-07-19       Impact factor: 2.952

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