Kidney lipid dysmetabolism and lipid droplet accumulation in chronic kidney disease

A Mitrofanova, S Merscher, A Fornoni - Nature Reviews Nephrology, 2023 - nature.com
Chronic kidney disease (CKD) is a global health problem with rising incidence and
prevalence. Among several pathogenetic mechanisms responsible for disease progression …

The glomerular filtration barrier: a structural target for novel kidney therapies

IS Daehn, JS Duffield - Nature Reviews Drug Discovery, 2021 - nature.com
Loss of normal kidney function affects more than 10% of the population and contributes to
morbidity and mortality. Kidney diseases are currently treated with immunosuppressive …

The key role of NLRP3 and STING in APOL1-associated podocytopathy

J Wu, A Raman, NJ Coffey, X Sheng… - The Journal of …, 2021 - Am Soc Clin Investig
Coding variants in apolipoprotein L1 (APOL1), termed G1 and G2, can explain most excess
kidney disease risk in African Americans; however, the molecular pathways of APOL1 …

The evolving story of apolipoprotein L1 nephropathy: the end of the beginning

P Daneshpajouhnejad, JB Kopp, CA Winkler… - Nature Reviews …, 2022 - nature.com
Genetic coding variants in APOL1, which encodes apolipoprotein L1 (APOL1), were
identified in 2010 and are relatively common among individuals of sub-Saharan African …

APOL1-mediated monovalent cation transport contributes to APOL1-mediated podocytopathy in kidney disease

S Datta, BM Antonio, NH Zahler… - The Journal of …, 2024 - Am Soc Clin Investig
Two coding variants of apolipoprotein L1 (APOL1), called G1 and G2, explain much of the
excess risk of kidney disease in African Americans. While various cytotoxic phenotypes have …

The contribution of lipotoxicity to diabetic kidney disease

JR Schelling - Cells, 2022 - mdpi.com
Lipotoxicity is a fundamental pathophysiologic mechanism in diabetes and non-alcoholic
fatty liver disease and is now increasingly recognized in diabetic kidney disease (DKD) …

Recessive, gain-of-function toxicity in an APOL1 BAC transgenic mouse model mirrors human APOL1 kidney disease

GM McCarthy, A Blasio, OG Donovan… - Disease Models & …, 2021 - journals.biologists.com
People of recent sub-Saharan African ancestry develop kidney failure much more frequently
than other groups. A large fraction of this disparity is due to two coding sequence variants in …

APOL1 and Kidney Disease: From Genetics to Biology

DJ Friedman, MR Pollak - Annual review of physiology, 2020 - annualreviews.org
Genetic variants in the APOL1 gene, found only in individuals of recent African ancestry,
greatly increase risk of multiple types of kidney disease. These APOL1 kidney risk alleles …

[HTML][HTML] Sirt6 deficiency aggravates angiotensin II-induced cholesterol accumulation and injury in podocytes

Q Yang, J Hu, Y Yang, Z Chen, J Feng, Z Zhu… - Theranostics, 2020 - ncbi.nlm.nih.gov
Disturbed renal lipid metabolism, especially cholesterol dysregulation plays a crucial role in
the pathogenesis of chronic kidney disease (CKD). We recently reported that angiotensin …

Autophagy and mitophagy: physiological implications in kidney inflammation and diseases

D Bhatia, ME Choi - American Journal of Physiology-Renal …, 2023 - journals.physiology.org
Autophagy is a ubiquitous intracellular cytoprotective quality control program that maintains
cellular homeostasis by recycling superfluous cytoplasmic components (lipid droplets …