Common Charge-Shift Mutation Glu65Lys in K+ Channel β1-Subunit KCNMB1: Pleiotropic Consequences for Glomerular Filtration Rate and Progressive Renal Disease
Author(s) -
Yuqing Chen,
Rany M. Salem,
Fangwen Rao,
Maple M. Fung,
Vibha Bhatnagar,
Braj Pandey,
Manjula Mahata,
Jill Waalen,
Caroline M. Nievergelt,
Michael S. Lipkowitz,
Bruce A. Hamilton,
Sushil K. Mahata,
Daniel T. O’Connor
Publication year - 2010
Publication title -
american journal of nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.394
H-Index - 85
eISSN - 1421-9670
pISSN - 0250-8095
DOI - 10.1159/000320131
Subject(s) - renal function , endocrinology , medicine , kidney disease
Glomerular filtration rate (GFR) is a heritable trait, and hyperfiltration (GFR increment in remnant nephrons) may accelerate renal functional decline in chronic kidney disease (CKD). Mesangial and vascular smooth myocytes control GFR by contraction, dependent on voltage-gated Ca(2+) influx, which is controlled by the regulatory β₁-subunit (KCNMB1) of large-conductance heteromeric K+ ('BK') channels. KCNMB1 gain-of-function variant Glu65Lys results in generalized vasorelaxation and thus protection against systemic hypertension. Here we asked whether the Glu65Lys variant influences GFR, in the basal state or during progressive renal decline.
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