van de Graaf Stan F J, van der Kemp Annemiete W C M, van den Berg Dennis, van Oorschot Mijke, Hoenderop Joost G J, Bindels René J M
Cell Physiology, Radboud University Nijmegen Medical Centre, PO Box 9101, NL-6500 HB Nijmegen, The Netherlands.
J Am Soc Nephrol. 2006 Jan;17(1):26-30. doi: 10.1681/ASN.2005101025.
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.
瞬时受体电位香草酸亚型5(TRPV5)和TRPV6是TRP超家族中对Ca2+选择性最高的成员,对上皮细胞中Ca2+的主动(再)吸收至关重要。然而,对于调节这些通道活性的细胞内蛋白却知之甚少。本研究确定BSPRY(含B盒和SPRY结构域的蛋白)是参与调控TRPV5的一个新因子。通过谷胱甘肽-S-转移酶(GST)下拉实验和免疫共沉淀实验证实了BSPRY与TRPV5之间的相互作用。在小鼠肾脏中,BSPRY与TRPV5共定位。在稳定表达TRPV5的Madin-Darby犬肾细胞中,BSPRY的表达导致Ca2+内流显著减少,而不影响通道在细胞表面的丰度。最后,在25-羟基维生素D3-1α-羟化酶基因敲除小鼠中,肾脏中BSPRY的表达增加,提示维生素D3对其有反向调节作用。总之,这些结果证明了新蛋白BSPRY通过对TRPV5活性的负调节在上皮细胞Ca2+转运调控中的生理作用。