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• W2146597955 endingPage "2128" @default.
• W2146597955 startingPage "2119" @default.
• W2146597955 abstract "In patients of African ancestry, genetic variants in APOL1, which encodes apolipoprotein L1, associate with the nondiabetic kidney diseases, focal segmental glomerulosclerosis (FSGS), HIV-associated nephropathy (HIVAN), and hypertensive nephropathy. Understanding the renal localization of APOL1 may provide clues that will ultimately help elucidate the mechanisms by which APOL1 variants promote nephropathy. Here, we used immunohistology to examine APOL1 localization in normal human kidney sections and in biopsies demonstrating either FSGS (n = 8) or HIVAN (n = 2). Within normal glomeruli, APOL1 only localized to podocytes. Compared with normal glomeruli, fewer cells stained for APOL1 in FSGS and HIVAN glomeruli, even when expression of the podocyte markers GLEPP1 and synaptopodin appeared normal. APOL1 localized to proximal tubular epithelia in normal kidneys, FSGS, and HIVAN. We detected APOL1 in the arteriolar endothelium of normal and diseased kidney sections. Unexpectedly, in both FSGS and HIVAN but not normal kidneys, the media of medium artery and arterioles contained a subset of α-smooth muscle actin-positive cells that stained for APOL1. Comparing the renal distribution of APOL1 in nondiabetic kidney disease to normal kidney suggests that a previously unrecognized arteriopathy may contribute to disease pathogenesis in patients of African ancestry." @default.
• W2146597955 created "2016-06-24" @default.
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• W2146597955 date "2011-10-13" @default.
• W2146597955 modified "2023-10-18" @default.
• W2146597955 title "APOL1 Localization in Normal Kidney and Nondiabetic Kidney Disease" @default.
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• W2146597955 doi "https://doi.org/10.1681/asn.2011010069" @default.
• W2146597955 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3231786" @default.
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• W2146597955 hasPublicationYear "2011" @default.
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