Sox6 as a new modulator of renin expression in the kidney

Author:

Saleem Mohammad1,Hodgkinson Conrad P.2,Xiao Liang1,Gimenez-Bastida Juan A.1ORCID,Rasmussen Megan L.3,Foss Jason1,Payne Alan J.2,Mirotsou Maria2,Gama Vivian3,Dzau Victor J.2,Gomez Jose A.1

Affiliation:

1. Department of Medicine/Clinical Pharmacology Division, Vanderbilt University Medical Center, Nashville, Tennessee

2. Department of Medicine, Duke University Medical Center, Durham, North Carolina

3. Department of Cell and Developmental Biology, Vanderbilt University, Nashville, Tennessee

Abstract

Juxtaglomerular (JG) cells, major sources of renin, differentiate from metanephric mesenchymal cells that give rise to JG cells or a subset of smooth muscle cells of the renal afferent arteriole. During periods of dehydration and salt deprivation, renal mesenchymal stromal cells (MSCs) differentiate from JG cells. JG cells undergo expansion and smooth muscle cells redifferentiate to express renin along the afferent arteriole. Gene expression profiling comparing resident renal MSCs with JG cells indicates that the transcription factor Sox6 is highly expressed in JG cells in the adult kidney. In vitro, loss of Sox6 expression reduces differentiation of renal MSCs to renin-producing cells. In vivo, Sox6 expression is upregulated after a low-Na+ diet and furosemide. Importantly, knockout of Sox6 in Ren1d+ cells halts the increase in renin-expressing cells normally seen during a low-Na+ diet and furosemide as well as the typical increase in renin. Furthermore, Sox6 ablation in renin-expressing cells halts the recruitment of smooth muscle cells along the afferent arteriole, which normally express renin under these conditions. These results support a previously undefined role for Sox6 in renin expression.

Funder

American Heart Association

HHS | NIH | National Heart, Lung, and Blood Institute

Publisher

American Physiological Society

Subject

Physiology

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