TRPC6 and FSGS: the latest TRP channelopathy - PubMed (original) (raw)
Review
. 2007 Aug;1772(8):859-68.
doi: 10.1016/j.bbadis.2007.03.005. Epub 2007 Mar 20.
Affiliations
- PMID: 17459670
- DOI: 10.1016/j.bbadis.2007.03.005
Free article
Review
TRPC6 and FSGS: the latest TRP channelopathy
Nirvan Mukerji et al. Biochim Biophys Acta. 2007 Aug.
Free article
Abstract
Focal and segmental glomerulosclerosis (FSGS) is a common cause of nephrotic syndrome in children and adults throughout the world. In the past 50 years, significant advances have been made in the identification and characterization of familial forms of nephrotic syndrome and FSGS. Resultant to these pursuits, several podocyte structural proteins such as nephrin, podocin, alpha-actinin 4 (ACTN4), and CD2-associated protein (CD2AP) have emerged to provide critical insight into the pathogenesis of hereditary nephrotic syndromes. The latest advance in familial FSGS has been the discovery of a mutant form of canonical transient receptor potential cation channel 6 (TRPC6), which causes an increase in calcium transients and essentially a gain of function in this cation channel located on the podocyte cell membrane. The TRP ion channel family is a diverse group of cation channels united by a common primary structure which contains six membrane-spanning domains, with both carboxy and amino termini located intracellularly. TRP channels are unique in their ability to activate independently of membrane depolarization. TRPC6 channels have been shown to be activated via phospholipase C stimulation. The mechanisms by which mutant TRPC6 causes an increase in intracellular calcium and leads to glomerulosclerosis are unknown. Mutant TRPC6 may affect critical interactions with the aforementioned podocyte structural proteins, leading to abnormalities in the slit diaphragm or podocyte foot processes. Mutant TRPC6 may also amplify injurious signals mediated by Ang II, a common final pathway of podocyte apoptosis in various mammalian species. Current evidence also suggests that blocking TRPC6 channels may be of therapeutic benefit in idiopathic FSGS, a disease with a generally poor prognosis. Preliminary experiments reveal the commonly used immunosuppressive agent FK-506 can inhibit TRPC6 activity in vivo. This creates the exciting possibility that blocking TRPC6 channels within the podocyte may translate into long-lasting clinical benefits in patients with FSGS.
Similar articles
- 2007 Young Investigator Award: TRP'ing into a new era for glomerular disease.
Winn MP. Winn MP. J Am Soc Nephrol. 2008 Jun;19(6):1071-5. doi: 10.1681/ASN.2007121292. Epub 2008 Apr 23. J Am Soc Nephrol. 2008. PMID: 18434567 - Regulation of TRPC6 ion channels in podocytes - Implications for focal segmental glomerulosclerosis and acquired forms of proteinuric diseases.
Szabó T, Ambrus L, Zákány N, Balla G, Bíró T. Szabó T, et al. Acta Physiol Hung. 2015 Sep;102(3):241-51. doi: 10.1556/036.102.2015.3.2. Acta Physiol Hung. 2015. PMID: 26551740 Review. - [The genetic basis of familial focal segmental glomerulosclerosis and related nephrotic syndrome].
Tsukaguchi H, Kitamura A. Tsukaguchi H, et al. Nihon Jinzo Gakkai Shi. 2007;49(2):88-97. Nihon Jinzo Gakkai Shi. 2007. PMID: 17375615 Japanese. No abstract available. - R168H and V165X mutant podocin might induce different degrees of podocyte injury via different molecular mechanisms.
Fan Q, Zhang H, Ding J, Liu S, Miao J, Xing Y, Yu Z, Guan N. Fan Q, et al. Genes Cells. 2009 Sep;14(9):1079-90. doi: 10.1111/j.1365-2443.2009.01336.x. Epub 2009 Aug 5. Genes Cells. 2009. PMID: 19674119 - Focal segmental glomerulosclerosis: molecular genetics and targeted therapies.
Chen YM, Liapis H. Chen YM, et al. BMC Nephrol. 2015 Jul 9;16:101. doi: 10.1186/s12882-015-0090-9. BMC Nephrol. 2015. PMID: 26156092 Free PMC article. Review.
Cited by
- Actin-associated Proteins in the Pathogenesis of Podocyte Injury.
He FF, Chen S, Su H, Meng XF, Zhang C. He FF, et al. Curr Genomics. 2013 Nov;14(7):477-84. doi: 10.2174/13892029113146660014. Curr Genomics. 2013. PMID: 24396279 Free PMC article. - Analysis of the clinical characteristics of arthritis with renal disease caused by a NPHS2 gene mutation.
Shi D, Zhang Y, Liu D, Xu L, Tang X. Shi D, et al. Clin Rheumatol. 2021 Aug;40(8):3335-3343. doi: 10.1007/s10067-020-05574-7. Epub 2021 Jan 11. Clin Rheumatol. 2021. PMID: 33428103 Review. - A new role for PTEN in regulating transient receptor potential canonical channel 6-mediated Ca2+ entry, endothelial permeability, and angiogenesis.
Kini V, Chavez A, Mehta D. Kini V, et al. J Biol Chem. 2010 Oct 22;285(43):33082-33091. doi: 10.1074/jbc.M110.142034. Epub 2010 Aug 12. J Biol Chem. 2010. PMID: 20705603 Free PMC article. - Differential expression of canonical (classical) transient receptor potential channels in guinea pig enteric nervous system.
Liu S, Qu MH, Ren W, Hu HZ, Gao N, Wang GD, Wang XY, Fei G, Zuo F, Xia Y, Wood JD. Liu S, et al. J Comp Neurol. 2008 Dec 20;511(6):847-62. doi: 10.1002/cne.21874. J Comp Neurol. 2008. PMID: 18925632 Free PMC article. - Photoswitchable TRPC6 channel activators evoke distinct channel kinetics reflecting different gating behaviors.
Keck M, Hermann C, Lützel K, Gudermann T, Konrad DB, Mederos Y Schnitzler M, Storch U. Keck M, et al. iScience. 2024 Sep 20;27(10):111008. doi: 10.1016/j.isci.2024.111008. eCollection 2024 Oct 18. iScience. 2024. PMID: 39403196 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous