4.5 Article

The calcium-sensing receptor couples to Gαs and regulates PTHrP and ACTH secretion in pituitary cells

期刊

JOURNAL OF ENDOCRINOLOGY
卷 204, 期 3, 页码 287-297

出版社

BIOSCIENTIFICA LTD
DOI: 10.1677/JOE-09-0183

关键词

-

资金

  1. NCI NIH HHS [R01 CA094175, R01 CA153702] Funding Source: Medline
  2. NIDDK NIH HHS [R01 DK055501, DK069542, R01 DK069542] Funding Source: Medline

向作者/读者索取更多资源

The calcium-sensing receptor (CaR or CASR as listed in the MGI Database) is a G protein-coupled receptor that binds and signals in response to extracellular calcium and other polycations. It is highly expressed on parathyroid and kidney cells, where it participates in the regulation of systemic calcium homeostasis. It is also expressed on many other cell types and is involved in a wide array of biological functions such as cell growth and differentiation, ion transport, and hormone secretion. It has been described to couple to several different G proteins including Ga-i/0, G alpha(q/11), and G alpha(12/13). Recently, it has also been shown to stimulate cAMP production by coupling to Gas in immortalized or malignant breast cells. The CaR is expressed on cells in the anterior pituitary and had previously been described to stimulate cAMP production in these cells. In this report, we examined signaling from the CaR in murine pituitary corticotroph-derived, AtT-20 cells. We found that CaR activation led to the stimulation of cAMP production, and PTH-related protein (PTHrP or PTHLH as listed in the MGI Database) and ACTH secretion from these cells. Furthermore, manipulation of cAMP levels was able to modulate PTHrP and ACTH secretion independent of changes in extracellular calcium. Finally, we demonstrated that the CaR couples to G alpha(s) in AtT-20 cells. Therefore, in pituitary corticotroph-like cells, as in breast cancer cells, the CaR utilizes G alpha(s) and activates cAMP production to stimulate hormone secretion. Journal of Endocrinology (2010) 204, 287-297

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据