首页|肌微管素相关微蛋白7在小鼠肺动脉高压中的作用及机制

肌微管素相关微蛋白7在小鼠肺动脉高压中的作用及机制

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目的 探讨肌微管素相关微蛋白7(myotubularin relat-ed protein 7,MTMR7)在肺动脉高压中的作用及机制。方法 健康♂小鼠、Mtmr7转基因(Mftmr7-Tg)小鼠各20只,分为对照组、Mtmr7-Tg 组、野百合碱(monocrotaline,MCT)组、MCT+Mtmr7-Tg组,超声测量肺动脉血流加速时间(pulmonary artery acceleration time,PAT)和射血时间(pulmonary artery e-jection time,PET),取材时分离右心室游离壁,计算右心肥厚指数,免疫染色观察肺小动脉重构。将小鼠肺动脉平滑肌细胞(pulmonary arterial smooth muscle cells,PASMCs)以低氧处理,观察其增殖和迁移情况。结果 MTMR7在肺血管中表达,并且MCT处理之后,Mtmr7-Tg小鼠的PAT/PET比值降低(P<0。05),右心肥厚指数升高(P<0。01)。以Mtmr7基因过表达腺病毒转染PASMCs,可以抑制其增殖和迁移。用chemerin-9恢复p-ERK1/2的活性,过表达 MTMR7对PASMCs增殖、迁移抑制作用消失。结论 过表达MTMR7可减轻低氧诱导的小鼠PASMCs增殖和迁移,从而逆转肺动脉高压,机制与MTMR7降低ERK1/2磷酸化密切相关。
Role and mechanism of myotubularin-related protein 7 in pulmonary hypertension in mice
Aim To investigate the role of myotubula-rin related protein 7(MTMR7)in the pathogenesis of pulmonary hypertension manifested by pulmonary vas-cular intimal thickening,right ventricular hypertrophy,progressive right heart failure and dysfunction.Meth-ods A total of 40 healthy male C57BL/6J mice and Mtmr7-transgenic(Mtmr7-Tg)mice were divided into the control group,Mtmr7-Tg group,monocrotaline(MCT)group and MCT+Mtmr7-Tg group.Pulmonary artery acceleration time(PAT)and pulmonary artery ejection time(PET)of the pulmonary artery were measured by ultrasound.When the free wall of the right ventricle was separated,the right heart hypertro-phy index(RVHI)was calculated.Pulmonary artery remodeling was observed by immunostaining.Mouse pulmonary artery smooth muscle cells(PASMCs)were cultured in hypoxic environment to induce the prolifer-ation and migration.Results MTMR7 was expressed in pulmonary vessels.Compared to the wild-type mice,Mtmr7-Tg mice showed increased PAT/PET ratio(P<0.05),reduced RVHI(P<0.01)after MCT stimu-lus.PASMCs were transfected with adenovirus encond-ing Mtmr7 gene,which inhibited proliferation and mi-gration of PASMCs.After restoring the activity of ERK1/2 by chemerin-9,the proliferation and migra-tion ability of PASMCs was elevated.Conclusions MTMR7 can counteract the growth and mobility of mouse PASMCs induced by hypoxia,thereby comba-ting pulmonary arterial hypertension via reducing ERK1/2 phosphorylation.

myotubularin-related proteins 7ERK1/2pulmonary vascular remodelingpulmonary artery smooth muscle cellspulmonary hypertensionright ventricular hypertrophy

王嘉、张黎、杨耀、杨曦、孙雄山、杨永健

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西南交通大学医学院

西部战区总医院心内科,四川成都 610083

西南医科大学临床医学院心血管内科,四川泸州 646000

西部战区总医院药剂科,四川成都 610083

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肌微管素相关微蛋白7 ERK1/2 肺血管重构 肺动脉平滑肌细胞 肺动脉高压 右心室肥厚

2025

中国药理学通报
中国药理学会

中国药理学通报

北大核心
影响因子:1.54
ISSN:1001-1978
年,卷(期):2025.41(1)