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DGAT2 Inhibition Potentiates Lipid Droplet Formation To Reduce Cytotoxicity in APOL1 Kidney Risk Variants.

Authors :
Chun J
Riella CV
Chung H
Shah SS
Wang M
Magraner JM
Ribas GT
Ribas HT
Zhang JY
Alper SL
Friedman DJ
Pollak MR
Source :
Journal of the American Society of Nephrology : JASN [J Am Soc Nephrol] 2022 May; Vol. 33 (5), pp. 889-907. Date of Electronic Publication: 2022 Mar 01.
Publication Year :
2022

Abstract

Background: Two variants in the gene encoding apolipoprotein L1 (APOL1) that are highly associated with African ancestry are major contributors to the large racial disparity in rates of human kidney disease. We previously demonstrated that recruitment of APOL1 risk variants G1 and G2 from the endoplasmic reticulum to lipid droplets leads to reduced APOL1-mediated cytotoxicity in human podocytes.<br />Methods: We used CRISPR-Cas9 gene editing of induced pluripotent stem cells to develop human-derived APOL1 <superscript>G0/G0</superscript> and APOL1 <superscript>G2/G2</superscript> kidney organoids on an isogenic background, and performed bulk RNA sequencing of organoids before and after treatment with IFN- γ . We examined the number and distribution of lipid droplets in response to treatment with inhibitors of diacylglycerol O-acyltransferases 1 and 2 (DGAT1 and DGAT2) in kidney cells and organoids.<br />Results: APOL1 was highly upregulated in response to IFN- γ in human kidney organoids, with greater increases in organoids of high-risk G1 and G2 genotypes compared with wild-type (G0) organoids. RNA sequencing of organoids revealed that high-risk APOL1 <superscript>G2/G2</superscript> organoids exhibited downregulation of a number of genes involved in lipogenesis and lipid droplet biogenesis, as well as upregulation of genes involved in fatty acid oxidation. There were fewer lipid droplets in unstimulated high-risk APOL1 <superscript>G2/G2</superscript> kidney organoids than in wild-type APOL1 <superscript>G0/G0</superscript> organoids. Whereas DGAT1 inhibition reduced kidney organoid lipid droplet number, DGAT2 inhibition unexpectedly increased organoid lipid droplet number. DGAT2 inhibition promoted the recruitment of APOL1 to lipid droplets, with associated reduction in cytotoxicity.<br />Conclusions: Lipogenesis and lipid droplet formation are important modulators of APOL1-associated cytotoxicity. Inhibition of DGAT2 may offer a potential therapeutic strategy to attenuate cytotoxic effects of APOL1 risk variants.<br /> (Copyright © 2022 by the American Society of Nephrology.)

Details

Language :
English
ISSN :
1533-3450
Volume :
33
Issue :
5
Database :
MEDLINE
Journal :
Journal of the American Society of Nephrology : JASN
Publication Type :
Academic Journal
Accession number :
35232775
Full Text :
https://doi.org/10.1681/ASN.2021050723