甲状旁腺激素
甲状旁腺主细胞
继发性甲状旁腺功能亢进
内分泌学
光遗传学
内科学
分泌物
刺激
骨化三醇
钙代谢
甲状旁腺功能亢进
生物学中的钙
化学
钙
生物
医学
神经科学
作者
Liu Yh,Lu Zhang,Nan Hu,Jie Shao,Dazhi Yang,Changshun Ruan,Shishu Huang,Li Ping Wang,William W. Lu,Xinzhou Zhang,Fan Yang
标识
DOI:10.1038/s41467-022-28472-9
摘要
Parathyroid hormone (PTH) plays crucial role in maintaining calcium and phosphorus homeostasis. In the progression of secondary hyperparathyroidism (SHPT), expression of calcium-sensing receptors (CaSR) in the parathyroid gland decreases, which leads to persistent hypersecretion of PTH. How to precisely manipulate PTH secretion in parathyroid tissue and underlying molecular mechanism is not clear. Here, we establish an optogenetic approach that bypasses CaSR to inhibit PTH secretion in human hyperplastic parathyroid cells. We found that optogenetic stimulation elevates intracellular calcium, inhibits both PTH synthesis and secretion in human parathyroid cells. Long-term pulsatile PTH secretion induced by light stimulation prevented hyperplastic parathyroid tissue-induced bone loss by influencing the bone remodeling in mice. The effects are mediated by light stimulation of opsin expressing parathyroid cells and other type of cells in parathyroid tissue. Our study provides a strategy to regulate release of PTH and associated bone loss of SHPT through an optogenetic approach.
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