机构地区:[1]延边大学,东北寒区肉牛科技创新教育部工程研究中心,吉林省肉牛科学与产业技术重大需求协同创新中心,延吉133002 [2]韩国江原大学校动物生命科学系,春川24341 [3]延边大学农学院动物医学系,延吉133002
出 处:《中国畜牧兽医》2022年第5期1840-1851,共12页China Animal Husbandry & Veterinary Medicine
基 金:国家自然科学基金资助项目(31660667);吉林省教育厅科学技术研究项目(JJKH20210590KJ);延边大学博士启动基金(602020078)。
摘 要:【目的】探究犬脂肪组织来源的间充质干细胞(cAd-MSCs)对重症急性胰腺炎(SAP)体外模型的抗凋亡作用,以期为利用干细胞治疗胰腺炎提供理论指导。【方法】①用Ⅰ型胶原酶消化分离cAd-MSCs,用流式细胞术鉴定其干细胞标志物CD29、CD34、CD44、CD45、CD73和CD90的表达,用成脂、成骨和成软骨分化来鉴定其多向分化潜能;②用Ⅰ型胶原酶从小鼠胰腺组织中分离胰腺腺泡细胞(PACs),用实时荧光定量PCR检测PACs及胰腺组织中胰腺导管特异性基因CK19、β-胰岛细胞特异性细胞基因Insulin-1、α-胰岛细胞特异性基因Glucagon及PAC特异性基因PTF-1α、CPA-1、AMY2B的表达;③以10、20μg/mL脂多糖(LPS),10、100 mmol/L雨蛙肽(Caerulein)以及10μg/mL LPS+100 mmol/L Caerulein处理PACs,不添加药物培养的细胞为对照组,培养24 h后使用CCK-8检测PACs存活率,筛选体外构建内质网应激模型的最佳处理组(即模型组,P);用CCK-8检测对照组(Naive)及模型组(P)细胞0、2、4、8、12和24 h的存活率,Western blotting检测P组细胞内质网应激相关蛋白的相对表达量;④为确定cAd-MSCs对PACs的作用方式,试验分为PAC组(仅PACs,Naive)、P组、间接共培养组(IC)、直接共培养组(构建PAC模型时与cAd-MSCs直接共培养,DC),用实时荧光定量PCR检测肿瘤坏死因子(TNF-α)基因在PACs中的表达水平;⑤在间接共培养系统中,将细胞分为空白对照组(仅PACs,Naive)、对照组(PACs与cAd-MSCs共培养,C)、P组及试验组(药物处理的PACs与cAd-MSCs细胞共培养,T),细胞培养12 h后,通过实时荧光定量PCR、Western blotting检测各组细胞内质网应激相关基因及蛋白表达水平的变化,并用TUNEL法检测各组细胞的凋亡情况。【结果】①分离培养的cAd-MSCs呈现成纤维样细胞形态,高表达干细胞标志物CD29、CD44、CD73及CD90,不表达CD34和CD45,且具备成脂、成骨、成软骨分化能力;②分离的原代PACs呈鹅卵石样,与胰腺组织相�【Objective】The aim of this study was to investigate the anti-apoptotic effect of canine adipose-derived mesenchymal stem cells(cAd-MSCs)on in vitro model of severe acute pancreatitis(SAP),in order to provide a theoretical guide for the treatment of pancreatitis with stem cells.【Method】①TypeⅠcollagenase digestion method was used to separate cAd-MSCs,the expression of stem cell markers CD29,CD34,CD44,CD45,CD73 and CD90 was identified by flow cytometry,and its multidirectional differentiation potential was identified by adipogenic,osteogenic and chondrogenic differentiation.②Pancreatic acinar cells(PACs)were isolated from mouse pancreatic tissue with typeⅠcollagenase.The expression of pancreatic duct-specific gene CK19,β-islet cell-specific gene Insulin-1,α-islet cell-specific gene Glucagon and PAC-specific genes PTF-1α,CPA-1 and AMY2B in PACs and pancreatic tissues were detected by Real-time quantitative PCR.③PACs were treated with 10 and 20μg/mL lipopolysaccharide(LPS),10 and 100 mmol/L Caerulein,and 10μg/mL LPS+100 mmol/L Caerulein,the cells cultured without drugs were used as the control group.The survival rate of PACs was detected by CCK-8 at 24 h to screen the optimal treatment group for constructing endoplasmic reticulum(ER)model in vitro(model group,P).The survival rate of control group(Naive)and P group were detected by CCK-8 at 0,2,4,8,12 and 24 h,the expression of ER stress-related proteins in P group were detected by Western blotting.④To determine the mode of action of cAd-MSCs on PACs,the experiment was divided into PAC group(only PACs,Naive),P group,indirect co-culture group(IC)and direct co-culture group(DC).The expression of TNF-αgene was detected by Real-time quantitative PCR.⑤In the IC system,cells were divided into blank control group(PACs only,Naive),control group(PACs co-cultured with cAd-MSCs),P group and experimental group(drug-treated PACs co-cultured with cAd-MSCs,T).The expression of ER stress-related genes and proteins were detected by Real-time quantitative PCR
关 键 词:犬脂肪来源的间充质干细胞(cAd-MSCs) 重症急性胰腺炎(SAP) 胰腺腺泡细胞(PACs) 雨蛙肽 脂多糖(LPS) 内质网应激
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