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甲状旁腺激素相关蛋白(PTHrP)对分离破骨细胞骨吸收作用的结构要求。

Structural requirements for the action of parathyroid hormone-related protein (PTHrP) on bone resorption by isolated osteoclasts.

作者信息

Evely R S, Bonomo A, Schneider H G, Moseley J M, Gallagher J, Martin T J

机构信息

St. Vincent's Institute of Medical Research, Melbourne, Australia.

出版信息

J Bone Miner Res. 1991 Jan;6(1):85-93. doi: 10.1002/jbmr.5650060114.

Abstract

Parathyroid hormone-related protein (PTHrP) plays a major role in the syndrome of humoral hypercalcemia of malignancy (HHM) by its actions on bone and kidney. In this study an isolated osteoclast bone resorption assay was used to investigate the actions of this peptide and the structure-activity relationships for its resorption effect. As with PTH, neither synthetic nor recombinant PTHrP preparations stimulated resorption within highly purified osteoclast populations. Resorption was stimulated only in the presence of contaminating osteoblasts or in cocultures with the osteoblast-like cell line UMR-106. In the presence of osteoblasts PTHrP-(1-34) and PTHrP-(1-84) stimulated bone resorption in a dose-dependent manner with a potency comparable to that of PTH-(1-34) on a molar basis. The biologic activity of the PTHrP was shown to reside in the first 34 amino acids, and within that region the structural requirements for promotion of osteoclastic resorption resembled closely those for promotion of cyclic AMP formation in osteoblast-like cells. Using emulsion autoradiography with iodinated PTHrP-(1-34) and PTHrP-(1-84) on mixed bone cell preparations from neonatal rats, specific binding was demonstrated only to osteoblasts, not to osteoclasts. These results clearly demonstrate that PTHrP is a potent stimulator of bone resorption and that these effects are, like those of PTH, mediated by initial actions upon cells of the osteoblast lineage.

摘要

甲状旁腺激素相关蛋白(PTHrP)通过作用于骨骼和肾脏,在恶性肿瘤体液性高钙血症综合征(HHM)中起主要作用。在本研究中,采用分离的破骨细胞骨吸收试验来研究该肽的作用及其吸收效应的构效关系。与甲状旁腺激素(PTH)一样,无论是合成的还是重组的PTHrP制剂,在高度纯化的破骨细胞群体中均未刺激骨吸收。仅在存在污染的成骨细胞时或与成骨细胞样细胞系UMR - 106共培养时,骨吸收才会受到刺激。在有成骨细胞存在的情况下,PTHrP - (1 - 34)和PTHrP - (1 - 84)以剂量依赖性方式刺激骨吸收,其效力在摩尔基础上与PTH - (1 - 34)相当。PTHrP的生物活性显示存在于前34个氨基酸中,并且在该区域内,促进破骨细胞吸收的结构要求与促进成骨细胞样细胞中环磷酸腺苷(cAMP)形成的结构要求非常相似。使用碘化的PTHrP - (1 - 34)和PTHrP - (1 - 84)对新生大鼠的混合骨细胞制剂进行乳胶放射自显影,结果表明特异性结合仅发生在成骨细胞上,而不是破骨细胞上。这些结果清楚地表明,PTHrP是骨吸收的有效刺激剂,并且这些作用,与PTH的作用一样,是通过对成骨细胞系细胞的初始作用介导的。

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