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发现σR/TMEM97作为动脉粥样硬化斑块的新型生物标志物:一项PET成像与验证研究。

Discovery of σR/TMEM97 as a Novel Biomarker for Atherosclerotic Plaques: A PET Imaging and Validation Study.

作者信息

Mou Tiantian, Wang Jingqi, Hu Biao, Gao Mingxin, Yun Mingkai, Gao Xu, Tian Yi, Li Haiyang, Jia Hongmei, Zhang Xiaoli, Huang Yiyun

机构信息

Department of Nuclear Medicine (T.M., B.H., M.Y., Y.T., X.Z.), Beijing Anzhen Hospital, Capital Medical University, China.

Key Laboratory of Radiopharmaceuticals (Beijing Normal University), Ministry of Education, College of Chemistry, Beijing Normal University, China (J.W., X.G., H.J.).

出版信息

Arterioscler Thromb Vasc Biol. 2025 Jul;45(7):1111-1123. doi: 10.1161/ATVBAHA.125.322721. Epub 2025 May 22.

Abstract

BACKGROUND

The aims of this study were to evaluate σR (sigma-2 receptor)/TMEM97 (transmembrane protein 97) expression in atherosclerotic plaques, and assess the feasibility of in vivo atherosclerotic plaques imaging using the σR/TMEM97 targeting probe 1-(4-(5,6-dimethoxyisoindolin-2-yl)butyl)-3-(2-[F]fluoroethyl)-1,3-dihydro-2-benzo[]imidazol-2-one ([F]SYB-NF) developed in our laboratory.

METHODS

Hematoxylin and eosin and immunohistochemical staining were performed on both human coronary endarterectomy specimens and mouse samples. The expression of σR/TMEM97 in RAW 264.7 cells incubated with ox-LDL (oxidized low-density lipoprotein) was analyzed using western blot analysis. Positron emission tomography imaging with [F]SYB-NF, [F]NaF, and 2-[F]fluoro-2-deoxy-d-glucose was conducted in wide-type C57BL/6 and ApoE mice. Specific binding was evaluated by coinjecting [F]SYB-NF with the σR/TMEM97 antagonist CM398 ([1-(4-(6,7-dimethoxy-3,4-dihydroisoquinolin-2(1)-yl)butyl)-3-methyl-1-benzo[]imidazol-2(3)-one]). Autoradiography and Oil Red O staining were performed on harvested aortas and corresponding sections.

RESULTS

Staining results demonstrated significant upregulatiaon of σR/TMEM97 expression at the early plaque formation and throughout the atherosclerosis progression. Western blot analysis indicated that incubation of macrophages with ox-LDL led to increased σR/TMEM97 expression. [F]SYB-NF specifically accumulated in the aortic arch of ApoE mice. Treatment with CM398 significantly reduced the standardized uptake value in the aortic arch of ApoE mice. [F]SYB-NF exhibited a higher standardized uptake value in the aortic arch (0.67±0.09 versus 0.51±0.07) and higher aortic arch-to-heart ratio (2.58 versus 0.56) in ApoE mice compared with 2-[F]fluoro-2-deoxy-d-glucose, and a higher aortic arch-to-bone ratio (2.24 versus 0.44) compared with [F]NaF. Autoradiography analysis revealed a strong correlation between the positive area in Oil Red O staining and autoradiography (Pearson correlation coefficient=0.993; =0.001), further supporting the association between elevated σR/TMEM97 expression and plaque formation.

CONCLUSIONS

σR/TMEM97 may serve as a potential biomarker for atherosclerotic plaques, and σR/TMEM97 positron emission tomography imaging may be used to monitor plaque formation and progression, as well as the efficacy of emerging therapeutic strategies for atherosclerotic plaques.

摘要

背景

本研究旨在评估σR(sigma-2受体)/TMEM97(跨膜蛋白97)在动脉粥样硬化斑块中的表达,并评估使用我们实验室开发的σR/TMEM97靶向探针1-(4-(5,6-二甲氧基异吲哚啉-2-基)丁基)-3-(2-[F]氟乙基)-1,3-二氢-2-苯并咪唑-2-酮([F]SYB-NF)对体内动脉粥样硬化斑块进行成像的可行性。

方法

对人类冠状动脉内膜切除术标本和小鼠样本进行苏木精-伊红染色和免疫组织化学染色。使用蛋白质免疫印迹分析来分析用氧化型低密度脂蛋白(ox-LDL)孵育的RAW 264.7细胞中σR/TMEM97的表达。用[F]SYB-NF、[F]NaF和2-[F]氟-2-脱氧-D-葡萄糖对野生型C57BL/6和载脂蛋白E(ApoE)小鼠进行正电子发射断层扫描成像。通过将[F]SYB-NF与σR/TMEM97拮抗剂CM398([1-(4-(6,7-二甲氧基-3,4-二氢异喹啉-2(1)-基)丁基)-3-甲基-1-苯并咪唑-2(3)-酮])共同注射来评估特异性结合。对收获的主动脉及其相应切片进行放射自显影和油红O染色。

结果

染色结果表明,在斑块形成早期及整个动脉粥样硬化进展过程中,σR/TMEM97表达显著上调。蛋白质免疫印迹分析表明,巨噬细胞与ox-LDL孵育导致σR/TMEM97表达增加。[F]SYB-NF特异性聚集在ApoE小鼠的主动脉弓中。用CM398处理显著降低了ApoE小鼠主动脉弓中的标准化摄取值。与2-[F]氟-2-脱氧-D-葡萄糖相比,[F]SYB-NF在ApoE小鼠的主动脉弓中表现出更高的标准化摄取值(0.67±0.09对0.51±0.07)和更高的主动脉弓与心脏比值(2.58对0.56),与[F]NaF相比,主动脉弓与骨骼比值更高(2.24对0.44)。放射自显影分析显示油红O染色的阳性区域与放射自显影之间存在很强的相关性(皮尔逊相关系数=0.993;P=0.001),进一步支持了σR/TMEM97表达升高与斑块形成之间的关联。

结论

σR/TMEM97可能作为动脉粥样硬化斑块的潜在生物标志物,并且σR/TMEM97正电子发射断层扫描成像可用于监测斑块形成和进展,以及新兴的动脉粥样硬化斑块治疗策略的疗效。

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