The Zinc Sensing Receptor, ZnR/GPR39, in Health and Disease

被引:87
作者
Hershfinkel, Michal [1 ,2 ]
机构
[1] Ben Gurion Univ Negev, Dept Physiol & Cell Biol, Fac Hlth Sci, POB 653, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Zlotowski Ctr Neurosci, Fac Hlth Sci, POB 653, IL-84105 Beer Sheva, Israel
基金
以色列科学基金会;
关键词
zinc; ZnR; GPR39; zinc signaling; neuron; keratinocyte; epithelium; intestine; colon; bone; CL-COTRANSPORTER KCC2; PANCREATIC BETA-CELLS; RAT CORTICAL-NEURONS; EXTRACELLULAR ZINC; BREAST-CANCER; UP-REGULATION; SYNAPTIC ZN2+; SERUM ZINC; ZN2+-SENSING RECEPTOR; RYANODINE RECEPTOR;
D O I
10.3390/ijms19020439
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
A distinct G-protein coupled receptor that senses changes in extracellular Zn2+, ZnR/GPR39, was found in cells from tissues in which Zn2+ plays a physiological role. Most prominently, ZnR/GPR39 activity was described in prostate cancer, skin keratinocytes, and colon epithelial cells, where zinc is essential for cell growth, wound closure, and barrier formation. ZnR/GPR39 activity was also described in neurons that are postsynaptic to vesicular Zn2+ release. Activation of ZnR/GPR39 triggers Gq-dependent signaling and subsequent cellular pathways associated with cell growth and survival. Furthermore, ZnR/GPR39 was shown to regulate the activity of ion transport mechanisms that are essential for the physiological function of epithelial and neuronal cells. Thus, ZnR/GPR39 provides a unique target for therapeutically modifying the actions of zinc in a specific and selective manner.
引用
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页数:19
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