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甲状旁腺激素/甲状旁腺激素相关蛋白配体与受体网络的功能分析。

Functional analysis of the PTH/PTHrP network of ligands and receptors.

作者信息

Kronenberg H M, Lanske B, Kovacs C S, Chung U I, Lee K, Segre G V, Schipani E, Jüppner H

机构信息

Endocrine Unit, Massachussetts General Hospital, Boston 02114, USA.

出版信息

Recent Prog Horm Res. 1998;53:283-301; discussion 301-3.

PMID:9769712
Abstract

Parathyroid hormone (PTH) and parathyroid hormone-related protein (PTHrP) are two related proteins that activate a common PTH/PTHrP receptor, yet have quite distinct physiologic missions. PTH is the major peptide regulator of blood calcium in higher vertebrates, while PTHrP predominantly acts as a paracrine regulator of differentiation and local intercellular signaling. To analyze the physiological roles of PTHrP and the PTH/PTHrP receptor, "knockout" mice missing either the PTHrP or the PTH/PTHrP receptor gene were developed. Both the PTHrP (-/-) mice and the PTH/PTHrP receptor (-/-) mice exhibit a growth plate chondrodysplasia that reflects accelerated differentiation of proliferating chondrocytes. Growth plate chondrocytes regulate the local production of PTHrP by secreting the protein, Indian hedgehog (Ihh), as they are leaving the proliferative pool. Ihh stimulates the production of PTHrP, which then slows the differentiation of chondrocytes, thereby delaying the production of Ihh. PTHrP also stimulates transport of calcium across the placenta. PTHrP (-/-) mice lack the normal elevation of fetal blood calcium (when compared to maternal levels) and have low placental transport of calcium. Fragments of PTHrP that do not bind to the PTH/PTHrP receptor can correct the defect of placental calcium transport in these mice. Thus, this action of PTHrP is not mediated by the PTH/PTHrP receptor. The "knockout" mice thus help delineate the roles of PTH. PTHrP, and the PTH/PTHrP receptor in an interacting network of ligands and receptors.

摘要

甲状旁腺激素(PTH)和甲状旁腺激素相关蛋白(PTHrP)是两种相关蛋白,它们激活共同的PTH/PTHrP受体,但具有截然不同的生理功能。PTH是高等脊椎动物血钙的主要肽调节剂,而PTHrP主要作为分化和局部细胞间信号传导的旁分泌调节剂。为了分析PTHrP和PTH/PTHrP受体的生理作用,人们培育出了缺失PTHrP或PTH/PTHrP受体基因的“基因敲除”小鼠。PTHrP(-/-)小鼠和PTH/PTHrP受体(-/-)小鼠均表现出生长板软骨发育异常,这反映了增殖软骨细胞分化加速。当生长板软骨细胞离开增殖池时,它们通过分泌蛋白质印度刺猬因子(Ihh)来调节PTHrP的局部产生。Ihh刺激PTHrP的产生,然后PTHrP减缓软骨细胞的分化,从而延迟Ihh的产生。PTHrP还刺激钙跨胎盘运输。PTHrP(-/-)小鼠缺乏胎儿血钙的正常升高(与母体水平相比),并且胎盘钙运输较低。不与PTH/PTHrP受体结合的PTHrP片段可以纠正这些小鼠胎盘钙运输的缺陷。因此,PTHrP的这一作用不是由PTH/PTHrP受体介导的。因此,“基因敲除”小鼠有助于阐明PTH、PTHrP和PTH/PTHrP受体在配体和受体相互作用网络中的作用。

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