1. Gq signaling causes glomerular injury by activating TRPC6.
- Author
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Wang L, Jirka G, Rosenberg PB, Buckley AF, Gomez JA, Fields TA, Winn MP, and Spurney RF
- Subjects
- Albuminuria chemically induced, Animals, Calcineurin metabolism, Diabetes Mellitus, Type 1 complications, Diabetes Mellitus, Type 1 genetics, Diabetic Nephropathies genetics, Diabetic Nephropathies metabolism, Diabetic Nephropathies pathology, GTP-Binding Protein alpha Subunits, Gq-G11 genetics, Gene Deletion, Genes, Reporter, Glomerulosclerosis, Focal Segmental chemically induced, Glomerulosclerosis, Focal Segmental pathology, HEK293 Cells, Humans, Kidney Glomerulus pathology, Kidney Tubules pathology, Mice, Mice, Mutant Strains, Mice, Transgenic, NFATC Transcription Factors metabolism, Podocytes metabolism, Point Mutation, Puromycin Aminonucleoside toxicity, Recombinant Fusion Proteins metabolism, Signal Transduction, TRPC Cation Channels biosynthesis, TRPC Cation Channels deficiency, TRPC Cation Channels genetics, TRPC6 Cation Channel, Tacrolimus pharmacology, GTP-Binding Protein alpha Subunits, Gq-G11 physiology, Glomerulosclerosis, Focal Segmental genetics, TRPC Cation Channels physiology
- Abstract
Familial forms of focal segmental glomerulosclerosis (FSGS) have been linked to gain-of-function mutations in the gene encoding the transient receptor potential channel C6 (TRPC6). GPCRs coupled to Gq signaling activate TRPC6, suggesting that Gq-dependent TRPC6 activation underlies glomerular diseases. Here, we developed a murine model in which a constitutively active Gq α subunit (Gq(Q209L), referred to herein as GqQ>L) is specifically expressed in podocytes and examined the effects of this mutation in response to puromycin aminonucleoside (PAN) nephrosis. We found that compared with control animals, animals expressing GqQ>L exhibited robust albuminuria, structural features of FSGS, and reduced numbers of glomerular podocytes. Gq activation stimulated calcineurin (CN) activity, resulting in CN-dependent upregulation of TRPC6 in murine kidneys. Deletion of TRPC6 in GqQ>L-expressing mice prevented FSGS development and inhibited both tubular damage and podocyte loss induced by PAN nephrosis. Similarly, administration of the CN inhibitor FK506 reduced proteinuria and tubular injury but had more modest effects on glomerular pathology and podocyte numbers in animals with constitutive Gq activation. Moreover, these Gq-dependent effects on podocyte injury were generalizable to diabetic kidney disease, as expression of GqQ>L promoted albuminuria, mesangial expansion, and increased glomerular basement membrane width in diabetic mice. Together, these results suggest that targeting Gq/TRPC6 signaling may have therapeutic benefits for the treatment of glomerular diseases.
- Published
- 2015
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