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破骨细胞样细胞表达受体活性修饰蛋白2:激光捕获显微切割技术的应用

Osteoclast-like cells express receptor activity modifying protein 2: application of laser capture microdissection.

作者信息

Nakamura M, Morimoto S, Yang Q, Hisamatsu T, Hanai N, Nakamura Y, Mori I, Kakudo K

机构信息

Second Department of Pathology, Wakayama Medical University, Kimiidera 811-1, Wakayama City, Wakayama, 641-0012, Japan.

出版信息

J Mol Endocrinol. 2005 Feb;34(1):257-61. doi: 10.1677/jme.1.01652.

Abstract

Receptor activity modifying proteins (RAMPs) act as receptor modulators that determine the ligand specificity of receptors for the calcitonin (CT) family. The purpose of this study was to analyze the expression of RAMPs in osteoclast-like cells using the laser capture microdissection (LCM) technique. Mouse bone marrow and spleen cells were co-cultured on a film designed for LCM. After 10 days, 250 osteoclast-like cells were captured using the LCM system. Total RNA from these cells was used to synthesize cDNA and RT-PCR analysis was performed. Osteoclast-like cells expressed CT receptor (CTR), CT receptor-like receptor (CRLR) and RAMP2, but did not express RAMP1 or RAMP3. These results indicated (1) that a pure population of osteoclast-like cells can be prepared by LCM and gene expression of this population can be analyzed by RT-PCR and (2) that RT-PCR shows that osteoclast-like cells express RAMP2, CTR and CRLR, suggesting the potential for adrenomedullin binding to osteoclast-like cells. This is the first report that osteoclast-like cells express RAMP2.

摘要

受体活性修饰蛋白(RAMPs)作为受体调节剂,可决定降钙素(CT)家族受体的配体特异性。本研究旨在利用激光捕获显微切割(LCM)技术分析破骨细胞样细胞中RAMPs的表达。将小鼠骨髓和脾细胞在专为LCM设计的膜上共培养。10天后,使用LCM系统捕获250个破骨细胞样细胞。从这些细胞中提取的总RNA用于合成cDNA,并进行逆转录聚合酶链反应(RT-PCR)分析。破骨细胞样细胞表达降钙素受体(CTR)、降钙素受体样受体(CRLR)和RAMP2,但不表达RAMP1或RAMP3。这些结果表明:(1)通过LCM可以制备出纯的破骨细胞样细胞群体,并且可以通过RT-PCR分析该群体的基因表达;(2)RT-PCR显示破骨细胞样细胞表达RAMP2、CTR和CRLR,提示肾上腺髓质素与破骨细胞样细胞结合的可能性。这是关于破骨细胞样细胞表达RAMP2的首次报道。

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