Alterations of adrenomedullin and its receptor system components in calcified vascular smooth muscle cells |
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Authors: | Pan Chun Shui Qi Yong Fen Wang Shu Heng Zhao Jing Bu Ding Fang Li Gui Zhong Tang Chao Shu |
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Affiliation: | a Institute of Cardiovascular Diseases, Peking University First Hospital, Beijing 100034, China b Department of Physiology and Pathophysiology, Peking University Health Science Center, Beijing 100083, China c Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing 100083, China |
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Abstract: | ![]() Vascular calcification is a common finding in many cardiovascular diseases. Paracrine/autocrine changes in calcified vessels, and the secreted factors participate in and play an important role in the progress of calcification. Adrenomedullin (ADM) is a potent vasodilator peptide secreted by vascular smooth muscle cells (VSMCs) and vascular endothelial cells. Recently, receptor activity-modifying proteins (RAMPs) have been shown to transport calcitonin receptor-like receptor (CRLR) to the cell surface to present either as CGRP receptor or ADM receptor. In this work, we explored the production of ADM, alterations and significance of ADM mRNA and its receptor system components—CRLR and RAMPs mRNA in calcified VSMCs. Our results showed that calcium content, 45Ca2+ uptake and alkaline phosphatases (ALPs) activity in calcified VSMCs were increased, respectively, compared with control VSMCs. Content of ADM in medium was increased by 99% (p<0.01). Furthermore, it was found that the levels of ADM, CRLR, RAMP2 and RAMP3 mRNA in calcified cells were elevated, respectively, compared with that of control. The elevated levels of CRLR, RAMP2 and RAMP3 mRNA were significant correlation with ADM mRNA (r=0.83, 0.92 and 0.93, respectively, all p's<0.01) in calcified VSMCs. The results show that calcified VSMCs generate an increased amount of ADM, up-regulate gene expressions of ADM and its receptor system components—CRLR, RAMP2 and RAMP3, suggesting an important role of ADM and its receptor system in the regulation of vascular calcification. |
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Keywords: | Calcification Vascular smooth muscle cells (VSMCs) ADM CRLR RAMPs |
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