Identification of BSPRY as a novel auxiliary protein inhibiting TRPV5 activity
Publication year
2006Author(s)
Number of pages
5 p.
Source
Journal of the American Society of Nephrology, 17, 1, (2006), pp. 26-30ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Physiology
Journal title
Journal of the American Society of Nephrology
Volume
vol. 17
Issue
iss. 1
Languages used
English (eng)
Page start
p. 26
Page end
p. 30
Subject
IGMD 9: Renal disorder; NCMLS 5: Membrane transport and intracellular motility; UMCN 5.4: Renal disordersAbstract
Transient receptor potential vallinoid 5 (TRPV5) and TRPV6 are the most Ca2+-selective members of the TRP superfamily and are essential for active Ca2+ (re)absorption in epithelia. However, little is known about intracellular proteins that regulate the activity of these channels. This study identified BSPRY (B-box and SPRY-domain containing protein) as a novel factor involved in the control of TRPV5. The interaction between BSPRY and TRPV5 by GST pull-down and co-immunoprecipitation assays was demonstrated. BSPRY showed co-localization with TRPV5 in mouse kidney. Expression of BSPRY resulted in a significant reduction of the Ca2+ influx in Madin-Darby Canine Kidney cells that stably express TRPV5 without affecting channel cell-surface abundance. Finally, BSPRY expression in kidney was increased in 25-hydroxyvitamin D3-1alpha-hydroxylase knockout mice, suggesting an inverse regulation by vitamin D3. Together, these results demonstrate the physiologic role of the novel protein BSPRY in the regulation of epithelial Ca2+ transport via negative modulation of TRPV5 activity.
This item appears in the following Collection(s)
- Academic publications [227207]
- Electronic publications [108520]
- Faculty of Medical Sciences [86711]
- Open Access publications [77768]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.