中国兽医学报2024,Vol.44Issue(8) :1674-1681.DOI:10.16303/j.cnki.1005-4545.2024.08.13

奶牛骨髓源单核巨噬细胞诱导培养方法建立鉴定及应用

Establishment,identification and application of induction culture method of mono-nuclear macrophages from cow bone marrow

王钰 杨效林 郭莉莉 龚鹏飞 吴敬泽 毛伟 张双翼 刘博 曹金山
中国兽医学报2024,Vol.44Issue(8) :1674-1681.DOI:10.16303/j.cnki.1005-4545.2024.08.13

奶牛骨髓源单核巨噬细胞诱导培养方法建立鉴定及应用

Establishment,identification and application of induction culture method of mono-nuclear macrophages from cow bone marrow

王钰 1杨效林 1郭莉莉 1龚鹏飞 1吴敬泽 1毛伟 1张双翼 1刘博 1曹金山1
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作者信息

  • 1. 内蒙古农业大学兽医学院,内蒙古呼和浩特 010018;农业农村部动物疾病临床诊疗技术重点实验室,内蒙古呼和浩特 010018
  • 折叠

摘要

为了建立奶牛骨髓源巨噬细胞的分离培养与鉴定方法,选用3种不同的培养基(RPMI-1640、DMEM、DMEM/F12)分别添加20%胎牛血清(FBS)、2.4%青-链霉素、1.2%谷氨酰胺(Gln)、M-CSF(20 μg/L)将奶牛骨髓中提取出的单核细胞诱导为巨噬细胞,再通过加入脂多糖(Lipolyaccharide,LPS)将诱导出的M0型巨噬细胞极化为M1型巨噬细胞,光学显微镜在第1、4、7天观察巨噬细胞形态,比较3种培养基对分化巨噬细胞的差异.同时探究了前列腺素D2(Prostaglandin D2,PGD2)-DP2受体途径对大肠杆菌(Escherichia coli)诱导细胞因子(IL-6、TNF-α)分泌及巨噬细胞吞噬功能的影响.结果显示,RPMI-1640培养基中培养的细胞形态变化最为明显,且数量较多.并能够检测到大量的单核巨噬细胞特征性标志物(M0标志物:CD11b、CD14;M1标志物:CD11b、CD80)的表达,M0和M1型巨噬细胞纯度分别为79.9%和93.5%.与空白对照组相比,E.coli感染组COX-2和H-PGDS基因表达显著升高;PGD2分泌量也显著上升(P<0.000 1).DP2受体抑制剂(CAY10471、CAY10595)能够显著抑制E.coli诱导促炎性细胞因子(IL-6、TNF-α)的分泌和显著增强巨噬细胞对E.coli的杀伤作用.结果表明,诱导的细胞具有巨噬细胞特有的形态学特征和免疫表型;E.coli可诱导巨噬细胞PGD2的产生,PGD2-DP2途径对E.coli感染的巨噬细胞细胞因子的分泌具有一定的调控作用.

Abstract

In order to establish the isolation,culture and identification method of cow bone marrow-derived macrophages,three different media(RPMI-1640,DMEM,DMEM/F12)were added with 20%fetal bovine serum(FBS),2.4%chlorine-streptomycin,1.2%glutamine(Gln),and M-CSF(20 ng/mL),respectively,to induce the monocytes extracted from the bone marrow of dairy cows to become macrophages.The induced M0 macrophages were polarized into M1-type macrophages by adding lipopolysaccharide(LPS).The morphology of macrophages was observed by optical mi-croscope at day 1,4 and 7,and the differences of differentiated macrophages between the three media were compared.The effects of prostaglandin D2(PGD2)-DP2 receptor pathway on the secre-tion of cytokines(IL-6,TNF-α)induced by Escherichia coli and phagocytosis of macrophages were also investigated.The results showed that the morphological changes of cells cultured in the medium of RPMI-1640 were the most obvious and the number was large.A large number of char-acteristic markers of mononuclear macrophages were detected(M0 markers:CD1 1b,CD14;M1 markers:CD11b,CD80)expression,M0 and M1 macrophage purity were 79.9%and 93.5%,re-spectively.COX-2 and H-PGDS gene expressions were significantly increased in E.coli group com-pared with the blank control group.The secretion of PGD2also increased significantly(P<0.000 1).DP2 receptor inhibitors(CAY10471,CAY10595)could significantly inhibit the secretion of E.coli in-duced pro-inflammatory cytokines(IL-6,TNF-α)and significantly enhance the killing effect of macrophages on E.coli.The above results showed that the induced cells had the characteristic mor-phology and immunophenotype of macrophages.E.coli can induce the production of PGD2 in mac-rophages,and the PGD2-DP2 pathway regulates the secretion of cytokines in E.coli infected macro-phages.

关键词

奶牛/骨髓源巨噬细胞/分离培养鉴定/PGD2

Key words

cow/bone marrow derived macrophages/isolation culture identification/PGD2

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基金项目

国家自然科学基金资助项目(32160851)

内蒙古自治区科技计划资助项目(2020GG0042)

出版年

2024
中国兽医学报
吉林大学

中国兽医学报

CSTPCDCSCD北大核心
影响因子:0.702
ISSN:1005-4545
参考文献量23
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