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骨钙素在血管钙化中的作用机制OA

Mechanisms of osteocalcin in vascular calcification

中文摘要英文摘要

目的 探讨骨钙素在血管钙化中的作用机制.方法 40只健康的SD雌性大鼠,随机分为5组,每组8只,分为正常组、假手术+钙化组、去卵巢+钙化组、骨钙素沉默组(去卵巢+钙化+骨钙素沉默)、沉默阴性对照组(去卵巢+钙化+阴性对照).除正常组外,其余各组均采用维生素D3诱导建立血管钙化模型.采用维生素D3诱导大鼠血管钙化模型,给予骨钙素沉默基因干预,检测大鼠血脂水平,Von Kossa染色检测血管钙化,RT-qPCR法和Western blot法分别检测骨钙素(BGP)骨转录因子(Runx2)基因和蛋白表达.结果 血脂水平:钙化血管组(假手术+钙化组、去卵巢+钙化组、骨钙素沉默组、沉默阴性对照组)LDL-C水平较正常组有升高趋势[F(4.35)=8.71,P<0.05];血管钙化程度:钙化血管组(假手术+钙化组、去卵巢+钙化组、骨钙素沉默组、沉默阴性对照组)较正常组血管中层出现明显钙化;当予以骨钙素沉默后,血管钙化较沉默阴性对照组显著减轻(P<0.05).基因及蛋白表达水平:钙化血管组(假手术+钙化组、去卵巢+钙化组、骨钙素沉默组、沉默阴性对照组)较正常组BGP、Runx2的mRNA及蛋白表达均增加(P<0.05),当予以BGP沉默后,BGP、Runx2的mRNA及蛋白表达较沉默阴性对照组也均降低[BGP mRNA:F(4.35)=357.20,P<0.05;Runx2 mRNA:F(4.35)=3 132.10,P<0.05;BGP 蛋白:F(4.35)=92.44,P<0.05;Runx2 蛋白:F(4.35)=87.25,P<0.05].结论 骨钙素参与血管钙化的发生、发展,可能通过增加Runx2表达促进血管钙化.

Objective To investigate the role and underlying mechanisms of osteocalcin in vascular calcification.Methods Forty healthy female Sprague-Dawley rats were randomly assigned to five groups(n=8 per group):normal group,sham-operated plus calcification group,ovariectomy plus calcification group,osteocalcin-silencing group(ovar-iectomy+calcification+osteocalcin silencing),and negative control silencing group(ovariectomy+calcification+negative control).Except for the normal group,vascular calcification was induced in all groups by vitamin D3 administra-tion.Osteocalcin gene silencing was performed in the osteocalcin-silencing group.Serum lipid profiles were measured.Vascular calcification was evaluated by Von Kossa staining.The mRNA and protein expression levels of osteocalcin(bone Gla protein,BGP)and runt-related transcription factor 2(Runx2)were determined using reverse transcription quantita-tive polymerase chain reaction(RT-qPCR)and Western blot analysis,respectively.Results Compared with the nor-mal group,low-density lipoprotein cholesterol(LDL-C)levels were significantly increased in all calcification groups,including the sham-operated plus calcification,ovariectomy plus calcification,osteocalcin-silencing,and negative con-trol groups(P<0.05).Von Kossa staining demonstrated marked medial vascular calcification in all calcification groups compared with the normal group.Osteocalcin silencing significantly attenuated vascular calcification compared with the negative control group(P<0.05).The mRNA and protein expression levels of BGP and Runx2 were significantly in-creased in all calcification groups compared with the normal group(P<0.05).Following osteocalcin silencing,both BGP and Runx2 mRNA and protein expression levels were significantly reduced compared with the negative control group(P<0.05).Conclusion Osteocalcin participates in the development and progression of vascular calcification and may pro-mote vascular calcification by upregulating Runx2 expression.

苗立坤;杨伟;陈素芬;李胜军;金焱;刘宏;陈章荣

漯河市中心医院心血管内科(河南漯河 462000)贵州医科大学附属医院心血管内科(贵州贵阳 550004)漯河市中心医院心血管内科(河南漯河 462000)漯河市中心医院心血管内科(河南漯河 462000)漯河市中心医院心血管内科(河南漯河 462000)大理大学第一附属医院心血管内科(云南大理 671000)贵州医科大学附属医院心血管内科(贵州贵阳 550004)

医药卫生

骨钙素血管钙化骨转录因子-2

osteocalcinvascular calcificationrunt-related transcription factor 2

《广东医学》 2026 (7)

1024-1029,6

国家自然科学基金资助项目(81960085)大理市科技局基金项目(2019KGB017)

10.13820/j.cnki.gdyx.20260037

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