miRNA-378a过表达巨噬细胞株复合胶原蛋白海绵:抗炎及促进组织修复  

miRNA-378a overexpression of macrophage cell line composite collagen sponge:anti-inflammation and tissue repair promotion

作　　者：王思凡 何惠宇[1,2] 杨泉 韩祥祯 Wang Sifan;He Huiyu;Yang Quan;Han Xiangzhen(Department of Stomatology of First Affiliated Hospital of Xinjiang Medical University(Affiliated Stomatological Hospital),Urumqi 830054,Xinjiang Uygur Autonomous Region,China;Institute of Stomatology of Xinjiang Uygur Autonomous Region,Urumqi 830054,Xinjiang Uygur Autonomous Region,China;Urumqi Stomatological Hospital of Xinjiang Uygur Autonomous Region,Urumqi 830000,Xinjiang Uygur Autonomous Region,China)

机构地区：[1]新疆医科大学第一附属医院(附属口腔医院)口腔修复种植科,新疆维吾尔自治区乌鲁木齐市830054 [2]新疆维吾尔自治区口腔医学研究所,新疆维吾尔自治区乌鲁木齐市830054 [3]新疆维吾尔自治区乌鲁木齐市口腔医院,新疆维吾尔自治区乌鲁木齐市830000

出　　处：《中国组织工程研究》2025年第4期789-799,共11页Chinese Journal of Tissue Engineering Research

基　　金：2021年新疆维吾尔自治区自然科学基金计划青年项目(2021D01C337),项目负责人:韩祥祯。

摘　　要：背景:巨噬细胞M1/M2极化方向的调节在组织工程应用中尤为关键,及时调控可最大程度地减少促炎、促进抗炎或组织愈合反应。目的:将慢病毒介导的miRNA-378a过表达巨噬细胞株复合胶原蛋白海绵回植入动物模型,据此检测免疫调节在体内环境中的相关表达水平等组织修复相关的指标,进一步阐明在体内环境中miRNA-378a是否促进巨噬细胞M2极化及其对免疫调节和组织修复的作用。方法:将慢病毒介导的miRNA-378a过表达巨噬细胞株、阴性对照病毒巨噬细胞株扩增、筛选,复苏培养巨噬细胞株后与胶原蛋白海绵共培养以此构成复合体,具体分组如下:①阳性组:过表达miRNA-378a巨噬细胞-胶原蛋白海绵复合体;②阴性组:阴性对照病毒介导的miRNA-378a巨噬细胞-胶原蛋白海绵复合体;③对照组:巨噬细胞-胶原蛋白海绵;④空白对照组:胶原蛋白海绵。通过免疫荧光及扫描电镜观察各组细胞密度、表型、黏附情况,后回植入小鼠背部皮下模型,分别于造模后4,7 d处死小鼠,通过大体观察、苏木精-伊红染色、Masson染色、免疫组化分析慢病毒介导的miRNA-378a过表达巨噬细胞胶原蛋白海绵复合体中巨噬细胞极化的方向及其对机体免疫调控、组织修复的作用。结果与结论:①免疫荧光镜下观察各组巨噬细胞株确实与胶原蛋白海绵形成复合体;②扫描电镜下慢病毒介导的miRNA-378a巨噬细胞(阳性组)较其他分组细胞密度增加,细胞出现球形、椭圆形及多边形分化,具有更多的伪足;③大体观察下总体7 d愈合好于4 d,慢病毒介导的miRNA-378a过表达巨噬细胞(阳性组)无论4,7 d愈合均好于其他分组;④苏木精-伊红染色、Masson染色下,慢病毒介导的miRNA-378a过表达巨噬细胞(阳性组)具有较多量的纤维细胞、毛细血管、成纤维细胞以及胶原纤维增生;⑤免疫组化显示,慢病毒介导的miRNA-378a过表达巨噬细胞(阳性组)无�BACKGROUND:The regulation of M1/M2 polarization direction of macrophages is particularly critical in tissue engineering applications,and timely regulation can minimize proinflammatory,anti-inflammatory,or tissue healing responses.OBJECTIVE:To implant lentivirus-mediated miRNA-378a macrophage strain complex collagen to detect the expression level of immune regulation in the in vivo environment,and further clarify the influence of miRNA-378a in promoting macrophage M2 polarization in immune regulation and tissue repair in the in vivo environment.METHODS:Lentivirus-mediated miRNA-378a overexpressing macrophage cell lines and negative control virus macrophage lines were amplified and screened,and the macrophage lines were recovered and cultured together with collagen sponge to form a composite scaffold,which was divided into the following groups:(1)Positive group:miRNA-378a overexpressing macrophage-collagen sponge composite;(2)negative group:negative control of virus-mediated miRNA-378a macrophage-collagen sponge composite;(3)control group:macrophage-collagen sponge;(4)blank control group:collagen sponge.The cell density,phenotype,and adhesion of each group were observed by immunofluorescence and scanning electron microscopy.The cells were implanted into the subcutaneous model of the back of mice,and the mice were sacrificed 4 and 7 days after modeling.The direction of macrophage polarization in the collagen sponge composite of macrophages with miRNA-378a overexpression mediated by lentivirus and its effect on immune regulation and tissue repair were analyzed by gross observation,hematoxylin-eosin staining,MASSON staining,and immunohistochemistry.RESULTS AND CONCLUSION:(1)Under immunofluorescence microscopy,the macrophage cell lines in each group were observed to form a composite scaffold with the collagen sponge.(2)Under scanning electron microscope,lentivirus-mediated miRNA-378a macrophages in the positive group proliferated in cell density,had spherical,elliptic and polygonal differentiation,and had more pseudofe

关 键 词：miRNA-378a 慢病毒转染 巨噬细胞极化 免疫调节 组织工程 

分 类 号：R459.9[医药卫生—治疗学] R318[医药卫生—临床医学] R392