ID | 111530 |
Title Alternative | Parathyroid cells : structure or Ca2+ sensing receptor
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Author |
Yoshimoto, Katsuhiko
The University of Tokushima
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Saito, Shiro
The University of Tokushima
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Keywords | Ca2+ sensing receptor
Parathyroid
G protein coupled receptor
Familial hypocalciuric hypercalcemia
Autosomal dominant hypocalcemia
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Content Type |
Journal Article
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Description | Using expression in Xenopus oocytes, Brown et al. cloned a bovine parathyroid Ca2+ sensing receptor (BoPCaRl). The 1,085 amino acid membrane protein is included in a class of putative seven transmembrane spanning structures that activate the phosphoinositol pathway through G proteins. Receptor activation presumably elevates intracellular Ca2+ to inhibit secretion of PTH. BoPCaRl has a big extracellular domain at the amino terminus. BoPCaRl is most similar to the metabotropic glutamate receptor. BoPCaRl mRNA is found in cells that have well known Ca2+ sensing function. Inheritance of one inactive Ca2+ sensing receptor gene causes familial hypocalciuric hypercalcemia (FHH) and autosomal dominant hypocalcemia. Mutations in the extracellular domain and in a portion of the third intracellular loop domain decrease the receptor’s sensitivity, causing FHH. Extracellular domain mutations increase the receptor’s activity at low Ca2+ concentration to cause autosomal familial hypocalcemia.
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Journal Title |
Japanese journal of clinical medicine
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ISSN | 00471852
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NCID | AN00198641
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Publisher | 日本臨牀社
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Volume | 53
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Issue | 4
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Start Page | 805
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End Page | 810
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Published Date | 1995-04
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EDB ID | |
FullText File | |
language |
jpn
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TextVersion |
Publisher
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departments |
Oral Sciences
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