Xu Cao, Ke Ma, Yuhao Tao, Deyang Xi, Fangyu Hu, Jingjing Li
{"title":"壳聚糖修饰Fe3O4纳米探针对巨噬细胞特异性靶向MRI及对ox-LDL诱导巨噬细胞发泡的抑制作用","authors":"Xu Cao, Ke Ma, Yuhao Tao, Deyang Xi, Fangyu Hu, Jingjing Li","doi":"10.30564/JAMS.V4I2.3039","DOIUrl":null,"url":null,"abstract":"Atherosclerosis (AS) is a primary cause of morbidity and mortality all over the world. Molecular imaging techniques can enable early localization and diagnosis of atherosclerosis plaques. Recent newly developed chitooligosaccharides (CSO) is considered to be capable of target mannose receptors on the surface of macrophages and to inhibit foam cell formation. Here we present a targeting magnetic resonance imaging (MRI) nanoprobe, which was successfully constructed with polyacrylic acid (PAA) modified nanometer iron oxide (Fe3O4) as the core, and coating with CSO molecules, possessing the abilities of targeted MRI and specifically inhibition of the formation of foamy macrophages in the atherosclerotic process. The experimental results showed that the distributions of PAA-Fe3O4 and CSO-PAA-Fe3O4 were uniform and the corresponding sizes were about 5.93 nm and 8.15 nm, respectively. The Fourier transform infrared spectra (FTIR) testified the CSO was coupled with PAA-Fe3O4 successfully. After coupled with CSO, the r1 of PAA-Fe3O4 was increased from 5.317 mM s-1 to 6.147 mM s-1, indicating their potential as MRI contrast agent. Oil Red O staining and total cholesterols (TC) determination showed that CSO-PAA-Fe3O4 could significantly inhibit the foaming process of RAW264.7 cells induced by oxidatively modified low density lipoprotein (ox-LDL). In vitro cellular MRI displayed that, compared with PAA-Fe3O4,CSO-PAA-Fe3O4 could lower the T1 relaxation time of RAW264.7 cells better. In summary, construction of CSO-PAA-Fe3O4 nanoprobe in this study could realize the targeted MRI of macrophages and inhibition of ox-LDL induced macrophage foaming process. This will provide a new avenue in the diagnosis and treatment of AS.","PeriodicalId":14958,"journal":{"name":"Journal of Advances in Medicine Science","volume":"88 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Specific Targeting MRI of Chitosan Oligosaccharide Modified Fe3O4 Nanoprobe on Macrophage and the Inhibition of Macrophage Foaming Induced by ox-LDL\",\"authors\":\"Xu Cao, Ke Ma, Yuhao Tao, Deyang Xi, Fangyu Hu, Jingjing Li\",\"doi\":\"10.30564/JAMS.V4I2.3039\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Atherosclerosis (AS) is a primary cause of morbidity and mortality all over the world. Molecular imaging techniques can enable early localization and diagnosis of atherosclerosis plaques. 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Oil Red O staining and total cholesterols (TC) determination showed that CSO-PAA-Fe3O4 could significantly inhibit the foaming process of RAW264.7 cells induced by oxidatively modified low density lipoprotein (ox-LDL). In vitro cellular MRI displayed that, compared with PAA-Fe3O4,CSO-PAA-Fe3O4 could lower the T1 relaxation time of RAW264.7 cells better. In summary, construction of CSO-PAA-Fe3O4 nanoprobe in this study could realize the targeted MRI of macrophages and inhibition of ox-LDL induced macrophage foaming process. 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引用次数: 0
摘要
动脉粥样硬化(AS)是世界范围内发病率和死亡率的主要原因。分子成像技术可以实现动脉粥样硬化斑块的早期定位和诊断。近年来新开发的壳寡糖(CSO)被认为能够靶向巨噬细胞表面的甘露糖受体并抑制泡沫细胞的形成。本文以聚丙烯酸(PAA)修饰的纳米氧化铁(Fe3O4)为核心,包覆CSO分子,成功构建了一种靶向磁共振成像(MRI)纳米探针,该探针具有靶向MRI和特异性抑制动脉粥样硬化过程中泡沫巨噬细胞形成的能力。实验结果表明,PAA-Fe3O4和CSO-PAA-Fe3O4分布均匀,尺寸分别约为5.93 nm和8.15 nm。傅里叶变换红外光谱(FTIR)证实了CSO与PAA-Fe3O4的成功耦合。与CSO偶联后,PAA-Fe3O4的r1从5.317 mM s-1增加到6.147 mM s-1,显示其作为MRI造影剂的潜力。油红O染色和总胆固醇(TC)测定表明,CSO-PAA-Fe3O4能显著抑制氧化修饰低密度脂蛋白(ox-LDL)诱导的RAW264.7细胞发泡过程。体外细胞MRI显示,与PAA-Fe3O4相比,CSO-PAA-Fe3O4能更好地降低RAW264.7细胞的T1松弛时间。综上所述,本研究构建的CSO-PAA-Fe3O4纳米探针可以实现巨噬细胞的靶向MRI,抑制ox-LDL诱导的巨噬细胞发泡过程。这将为AS的诊断和治疗提供新的途径。
Specific Targeting MRI of Chitosan Oligosaccharide Modified Fe3O4 Nanoprobe on Macrophage and the Inhibition of Macrophage Foaming Induced by ox-LDL
Atherosclerosis (AS) is a primary cause of morbidity and mortality all over the world. Molecular imaging techniques can enable early localization and diagnosis of atherosclerosis plaques. Recent newly developed chitooligosaccharides (CSO) is considered to be capable of target mannose receptors on the surface of macrophages and to inhibit foam cell formation. Here we present a targeting magnetic resonance imaging (MRI) nanoprobe, which was successfully constructed with polyacrylic acid (PAA) modified nanometer iron oxide (Fe3O4) as the core, and coating with CSO molecules, possessing the abilities of targeted MRI and specifically inhibition of the formation of foamy macrophages in the atherosclerotic process. The experimental results showed that the distributions of PAA-Fe3O4 and CSO-PAA-Fe3O4 were uniform and the corresponding sizes were about 5.93 nm and 8.15 nm, respectively. The Fourier transform infrared spectra (FTIR) testified the CSO was coupled with PAA-Fe3O4 successfully. After coupled with CSO, the r1 of PAA-Fe3O4 was increased from 5.317 mM s-1 to 6.147 mM s-1, indicating their potential as MRI contrast agent. Oil Red O staining and total cholesterols (TC) determination showed that CSO-PAA-Fe3O4 could significantly inhibit the foaming process of RAW264.7 cells induced by oxidatively modified low density lipoprotein (ox-LDL). In vitro cellular MRI displayed that, compared with PAA-Fe3O4,CSO-PAA-Fe3O4 could lower the T1 relaxation time of RAW264.7 cells better. In summary, construction of CSO-PAA-Fe3O4 nanoprobe in this study could realize the targeted MRI of macrophages and inhibition of ox-LDL induced macrophage foaming process. This will provide a new avenue in the diagnosis and treatment of AS.