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甲状旁腺、肾脏及其他组织中的细胞外钙敏感受体。

Extracellular calcium-sensing receptors in the parathyroid gland, kidney, and other tissues.

作者信息

Quarles L Darryl

机构信息

Center for Bone and Mineral Disorders, Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Curr Opin Nephrol Hypertens. 2003 Jul;12(4):349-55. doi: 10.1097/00041552-200307000-00002.

Abstract

PURPOSE OF REVIEW

The discovery of the extracellular calcium-sensing receptor, CasR has broadened our understanding of calcium homeostasis and led to the development of new pharmacological agents, calcimimetics, for treating hyperparathyroidism. In the present review, I discuss the function of CasR as well as provide evidence for the presence of additional calcium-sensing mechanisms in the skeleton and possibly other tissues.

RECENT FINDINGS

Inactivating and activating mutations of the CasR respectively cause hereditary hyperparathyroidism, and demonstrate the predominant role of the CasR in controlling parathyroid gland function. Calcimimetics, which increase the sensitivity of CasR to extracellular calcium have been developed to treat secondary and primary hyperparathyroidism. In recent clinical trials in patients with end stage kidney disease, the calcimimetic cinacalcet suppressed parathyroid hormone to a greater degree than conventional therapy with vitamin D analogues without causing hypercalcemia or hyperphosphatemia. CasR receptor also has functions in other tissues, including regulation of renal calcium excretion and calcitonin secretion by thyroidal C-cells, but the presence of redundant sensing mechanisms for extracellular calcium in other tissues, including bone, confounds the assessment of the receptor's function at these sites. Mouse genetic approaches have so far failed to identify any essential, non-redundant role for the calcium-sensing receptor in regulating chondrogenesis or osteogenesis, and have failed to establish a function for the protein outside of the parathyroid gland, kidney, and thyroidal C-cells. Rather, there is evidence for other putative calcium sensing receptor-like mechanisms in osteoblasts that remain to be identified.

SUMMARY

Sensing of extracellular calcium by CasR is important in regulating calcium homeostasis, but CasR may have vestigial function in various tissues where it is expressed in low abundance. The relative importance of CasR and the novel calcium-sensing mechanisms in mediating response to extracellular calcium in many of these tissues remain to be determined.

摘要

综述目的

细胞外钙敏感受体(CasR)的发现拓宽了我们对钙稳态的认识,并促使新型药物拟钙剂的研发,用于治疗甲状旁腺功能亢进症。在本综述中,我将探讨CasR的功能,并提供证据证明在骨骼及其他可能的组织中存在额外的钙传感机制。

最新发现

CasR的失活和激活突变分别导致遗传性甲状旁腺功能亢进症,证明了CasR在控制甲状旁腺功能中的主要作用。已研发出拟钙剂,可提高CasR对细胞外钙的敏感性,用于治疗继发性和原发性甲状旁腺功能亢进症。在近期针对终末期肾病患者的临床试验中,拟钙剂西那卡塞比传统的维生素D类似物疗法更能有效抑制甲状旁腺激素,且不会引起高钙血症或高磷血症。CasR受体在其他组织中也具有功能,包括调节肾脏钙排泄以及甲状腺C细胞的降钙素分泌,但在包括骨骼在内的其他组织中,细胞外钙的冗余传感机制的存在,使得评估该受体在这些部位的功能变得复杂。迄今为止,小鼠遗传学方法未能确定钙敏感受体在调节软骨生成或骨生成方面有任何必要的、非冗余的作用,也未能确定该蛋白在甲状旁腺、肾脏和甲状腺C细胞之外的功能。相反,有证据表明成骨细胞中存在其他尚未确定的假定钙敏感受体样机制。

总结

CasR对细胞外钙的感知在调节钙稳态中很重要,但CasR在各种低丰度表达的组织中可能具有残余功能。CasR和新型钙传感机制在介导许多这些组织对细胞外钙反应中的相对重要性仍有待确定。

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