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胰岛淀粉样多肽在骨骼中的作用机制。

Mechanism of action of amylin in bone.

作者信息

Tamura T, Miyaura C, Owan I, Suda T

机构信息

Department of Biochemistry, School of Dentistry, Showa University, Tokyo, Japan.

出版信息

J Cell Physiol. 1992 Oct;153(1):6-14. doi: 10.1002/jcp.1041530103.

Abstract

Amylin is a 37 amino acid peptide produced mainly by beta-cells of the endocrine pancreas. Human amylin has 43% homology with human calcitonin gene-related peptide (CGRP) and 13% homology with human calcitonin (CT). Amylin and CGRP have been reported to have CT-like hypocalcemic activity in vivo. To investigate the role of amylin in bone, we examined the mechanisms of action of human amylin, CGRP, and CT in osteoclasts and osteoblasts. Both human amylin and CGRP inhibited 1 alpha,25-dihydroxyvitamin D3 [1 alpha,25(OH)2D3]- induced bone resorption in an organ culture system, and the potencies of the two peptides were similarly approximately 60-fold lower than that of human CT. Using a recently developed procedure for preparing large numbers of osteoclast-like multinucleated cells (MNCs) formed in co-cultures of mouse osteoblasts and bone marrow cells in the presence of 1 alpha,25(OH)2D3, we found that both human amylin and CGRP stimulated cAMP production in osteoclast-like MNCs, but only at 60-fold higher concentrations than human CT. Specific binding of [125I]-human CT to osteoclast-like MNCs was detected (dissociation constant, 3 x 10(-8) M; binding sites, 3 x 10(7) per cell). To displace the bound [125I]-human CT from osteoclast-like MNCs, about 170-fold higher concentrations of human amylin and CGRP were required. No specific bindings of [125I]-amylin and [125I]-CGRP to osteoclast-like MNCs could be detected. Human CGRP stimulated cAMP production both in established mouse osteoblast-like cells (KS-4) and in mouse primary osteoblast-like cells. Amylin was a weak agonist for cAMP production in KS-4 cells. The increment in cAMP production induced by CGRP and amylin was abolished by the addition of human CGRP(8-37), a selective antagonist for CGRP receptors. CT did not stimulate cAMP production in KS-4 cells. Amylin, but not CT, displaced the bound [125I]-human CGRP from rat brain membranes. These results indicate that amylin binds not only to CT receptors in osteoclast-like MNCs but also to CGRP receptors in osteoblasts. The relative potencies of these compounds to induce cAMP production was CT greater than amylin not equal to CGRP in osteoclast-like MNCs and CGRP greater amylin much greater than CT in osteoblast-like cells.

摘要

胰淀素是一种由内分泌胰腺的β细胞主要产生的含37个氨基酸的肽。人胰淀素与人降钙素基因相关肽(CGRP)有43%的同源性,与人降钙素(CT)有13%的同源性。据报道,胰淀素和CGRP在体内具有类似CT的降钙活性。为了研究胰淀素在骨骼中的作用,我们研究了人胰淀素、CGRP和CT在破骨细胞和成骨细胞中的作用机制。在器官培养系统中,人胰淀素和CGRP均抑制1α,25-二羟基维生素D3[1α,25(OH)2D3]诱导的骨吸收,且这两种肽的效力同样比人CT低约60倍。使用最近开发的一种方法,即在1α,25(OH)2D3存在的情况下,从小鼠成骨细胞和骨髓细胞共培养物中制备大量破骨细胞样多核细胞(MNCs),我们发现人胰淀素和CGRP均刺激破骨细胞样MNCs中cAMP的产生,但所需浓度比人CT高60倍。检测到[125I]-人CT与破骨细胞样MNCs的特异性结合(解离常数,3×10(-8)M;结合位点,每个细胞3×10(7)个)。为了从破骨细胞样MNCs中置换结合的[125I]-人CT,需要约170倍浓度更高的人胰淀素和CGRP。未检测到[125I]-胰淀素和[125I]-CGRP与破骨细胞样MNCs的特异性结合。人CGRP在已建立的小鼠成骨细胞样细胞(KS-4)和小鼠原代成骨细胞样细胞中均刺激cAMP的产生。胰淀素是KS-4细胞中cAMP产生的弱激动剂。添加人CGRP(8-37)(一种CGRP受体的选择性拮抗剂)可消除CGRP和胰淀素诱导的cAMP产生的增加。CT在KS-4细胞中不刺激cAMP的产生。胰淀素而非CT能从大鼠脑膜中置换结合的[125I]-人CGRP。这些结果表明,胰淀素不仅与破骨细胞样MNCs中的CT受体结合,还与成骨细胞中的CGRP受体结合。在破骨细胞样MNCs中,这些化合物诱导cAMP产生的相对效力为CT大于胰淀素不等于CGRP,而在成骨细胞样细胞中为CGRP大于胰淀素远大于CT。

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