A novel TRPC6 mutation that causes childhood FSGS

Saskia F. Heeringa, Clemens C. Möller, Jianyang Du, Lixia Yue, Bernward Hinkes, Gil Chernin, Christopher N. Vlangos, Peter F. Hoyer, Jochen Reiser, Fredhelm Hildebrandt

Research output: Contribution to journalArticlepeer-review

137 Scopus citations

Abstract

Background: TRPC6, encoding a member of the transient receptor potential (TRP) superfamily of ion channels, is a calcium-permeable cation channel, which mediates capacitive calcium entry into the cell. Until today, seven different mutations in TRPC6 have been identified as a cause of autosomal-dominant focal segmental glomerulosclerosis (FSGS) in adults. Methodology/Principal Findings: Here we report a novel TRPC6 mutation that leads to early onset FSGS. We identified one family in whom disease segregated with a novel TRPC6 mutation (M132T), that also affected pediatric individuals as early as nine years of age. Twenty-one pedigrees compatible with an autosomal-dominant mode of inheritance and biopsy-proven FSGS were selected from a worldwide cohort of 550 families with steroid resistant nephrotic syndrome (SRNS). Whole cell current recordings of the mutant TRPC6 channel, compared to the wild-type channel, showed a 3 to 5-fold increase in the average out- and inward TRPC6 current amplitude. The mean inward calcium current of M132T was 10-fold larger than that of wild-type TRPC6. Interestingly, M132T mutants also lacked time-dependent inactivation. Generation of a novel double mutant M132T/N143S did not further augment TRPC6 channel activity. Conclusions: In summary, our data shows that TRPC6 mediated FSGS can also be found in children. The large increase in channel currents and impaired channel inactivation caused by the M132T mutant leads to an aggressive phenotype that underlines the importance of calcium dose channeled through TRPC6.

Original languageEnglish (US)
Article numbere7771
JournalPloS one
Volume4
Issue number11
DOIs
StatePublished - Nov 10 2009
Externally publishedYes

ASJC Scopus subject areas

  • General

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