Laboratory of Veterinary Pharmacology, School of Veterinary Medicine, Kitasato University, Higashi 23 Bancho 35-1, Towada, Aomori, 034-8628, Japan.
Pflugers Arch. 2020 Mar;472(3):335-342. doi: 10.1007/s00424-019-02345-5. Epub 2020 Jan 21.
Chemerin is an adipocytokine having cardiovascular effects. Chemokine-like receptor 1 (CMKLR1) and chemokine (CC motif) receptor-like 2 (CCRL2) are chemerin receptors. Chemerin-9, an active fragment, causes contraction via smooth muscle CMKLR1 in isolated blood vessels. Pulmonary arterial hypertension (PAH) is a fatal disease resulting ultimately in right heart failure. To test the hypothesis that chemerin affects pulmonary artery (PA) resistance, we examined the effects of chemerin-9 on contractility of isolated PA from PAH rats. Wistar rats were injected with monocrotaline (MCT) for 2 weeks to make PAH rats (MCT rats). Control (Cont) rats received a saline injection. Chemerin-9-induced contraction of isolated intrapulmonary artery (IPA) from left lung was isometrically measured. Protein expression of CMKLR1 and CCRL2 in isolated left lung was determined by Western blotting. Localization of CMKLR1 in IPA of left lung was examined immunohistochemically. Chemerin-9-induced contraction was significantly enhanced in IPA from MCT compared with Cont rats. Protein expression of CMKLR1 was significantly elevated in isolated left lung from MCT compared with Cont rats, while protein expression of CCRL2, a decoy receptor, was significantly decreased. CMKLR1 was localized mainly in endothelium of IPA in Cont rats. The CMKLR1 expression was significantly decreased in endothelium of IPA in MCT rats, while it was significantly elevated in smooth muscle. The present study for the first time demonstrated that the enhanced chemerin-9-induced contraction of isolated IPA from MCT rats was at least partly caused by the increase of CMKLR1 in smooth muscle.
趋化素是一种具有心血管作用的脂肪细胞因子。趋化因子样受体 1(CMKLR1)和趋化因子(CC 基序)受体样 2(CCRL2)是趋化素受体。活性片段趋化素-9 通过分离血管中的平滑肌 CMKLR1 引起收缩。肺动脉高压(PAH)是一种致命疾病,最终导致右心衰竭。为了检验趋化素影响肺动脉(PA)阻力的假设,我们研究了趋化素-9 对 PAH 大鼠分离 PA 收缩性的影响。Wistar 大鼠接受单克隆松弛素(MCT)注射 2 周以制造 PAH 大鼠(MCT 大鼠)。对照(Cont)大鼠接受生理盐水注射。通过等长测量从左肺分离的肺内动脉(IPA)来测量趋化素-9 诱导的收缩。通过 Western 印迹法测定分离的左肺中 CMKLR1 和 CCRL2 的蛋白表达。用免疫组织化学法检查左肺 IPA 中 CMKLR1 的定位。与 Cont 大鼠相比,MCT 大鼠 IPA 中趋化素-9 诱导的收缩明显增强。与 Cont 大鼠相比,MCT 大鼠分离的左肺中 CMKLR1 的蛋白表达显著升高,而诱饵受体 CCRL2 的蛋白表达显著降低。CMKLR1 主要定位于 Cont 大鼠 IPA 的内皮中。在 MCT 大鼠 IPA 的内皮中,CMKLR1 的表达明显降低,而在平滑肌中则明显升高。本研究首次证明,MCT 大鼠分离 IPA 中趋化素-9 诱导的收缩增强至少部分是由平滑肌中 CMKLR1 的增加引起的。