滨州医学院学报
濱州醫學院學報
빈주의학원학보
JOURNAL OF BINZHOU MEDICAL COLLEGE
2013年
6期
401-404
,共4页
于国华%王威%冯国营%曲桂梅%姚卫东%郎志强%孔令玲
于國華%王威%馮國營%麯桂梅%姚衛東%郎誌彊%孔令玲
우국화%왕위%풍국영%곡계매%요위동%랑지강%공령령
褐藻多糖硫酸酯%TGF-β1%肾小管上皮细胞%转分化%细胞角蛋白%α-平滑肌肌动蛋白
褐藻多糖硫痠酯%TGF-β1%腎小管上皮細胞%轉分化%細胞角蛋白%α-平滑肌肌動蛋白
갈조다당류산지%TGF-β1%신소관상피세포%전분화%세포각단백%α-평활기기동단백
Fucoidan%TGF-β1%Human renal tubular epithelial cell%Epithelial mesenchymal transition%Cytokeratin%α-smooth mus-cle action
目的:通过体外观察褐藻多糖硫酸酯对TGF-β1诱导肾小管上皮细胞(HK-2)间质转分化过程中细胞角蛋白(cytok-eratin,CK)和α-平滑肌肌动蛋白(α-smooth muscle action ,α-SMA)表达的影响,探讨该药对HK-2上皮-间质转分化的影响及其作用机制。方法体外培养正常人肾小管上皮细胞( HK-2)细胞株,采用倒置相差显微镜观察对照组、诱导组和药物组细胞形态的变化,免疫细胞化学SABC法和图像分析技术检测培养第3 d对照组、诱导组和药物组HK-2细胞CK和α-SMA阳性细胞的平均光密度值。结果培养第3 d,对照组HK-2细胞呈现铺路石样上皮细胞形态特点,诱导组细胞呈长梭形,类似纤维细胞,药物组细胞以上皮细胞为主,少数细胞呈梭形;与对照组相比较,诱导组CK阳性细胞平均光密度值显著降低( P<0.05),α-SMA阳性细胞平均光密度值增加(P<0.05);与诱导组相比较,药物组CK阳性细胞平均光密度值显著增加(P<0.05),α-SMA阳性细胞平均光密度值显著降低(P<0.05)。结论①褐藻多糖硫酸酯具有抑制TGF-β1体外诱导的肾小管上皮细胞间质转分化的作用;②褐藻多糖硫酸酯可能通过改变细胞骨架成分发挥抑制肾小管上皮细胞间质转分化作用。
目的:通過體外觀察褐藻多糖硫痠酯對TGF-β1誘導腎小管上皮細胞(HK-2)間質轉分化過程中細胞角蛋白(cytok-eratin,CK)和α-平滑肌肌動蛋白(α-smooth muscle action ,α-SMA)錶達的影響,探討該藥對HK-2上皮-間質轉分化的影響及其作用機製。方法體外培養正常人腎小管上皮細胞( HK-2)細胞株,採用倒置相差顯微鏡觀察對照組、誘導組和藥物組細胞形態的變化,免疫細胞化學SABC法和圖像分析技術檢測培養第3 d對照組、誘導組和藥物組HK-2細胞CK和α-SMA暘性細胞的平均光密度值。結果培養第3 d,對照組HK-2細胞呈現鋪路石樣上皮細胞形態特點,誘導組細胞呈長梭形,類似纖維細胞,藥物組細胞以上皮細胞為主,少數細胞呈梭形;與對照組相比較,誘導組CK暘性細胞平均光密度值顯著降低( P<0.05),α-SMA暘性細胞平均光密度值增加(P<0.05);與誘導組相比較,藥物組CK暘性細胞平均光密度值顯著增加(P<0.05),α-SMA暘性細胞平均光密度值顯著降低(P<0.05)。結論①褐藻多糖硫痠酯具有抑製TGF-β1體外誘導的腎小管上皮細胞間質轉分化的作用;②褐藻多糖硫痠酯可能通過改變細胞骨架成分髮揮抑製腎小管上皮細胞間質轉分化作用。
목적:통과체외관찰갈조다당류산지대TGF-β1유도신소관상피세포(HK-2)간질전분화과정중세포각단백(cytok-eratin,CK)화α-평활기기동단백(α-smooth muscle action ,α-SMA)표체적영향,탐토해약대HK-2상피-간질전분화적영향급기작용궤제。방법체외배양정상인신소관상피세포( HK-2)세포주,채용도치상차현미경관찰대조조、유도조화약물조세포형태적변화,면역세포화학SABC법화도상분석기술검측배양제3 d대조조、유도조화약물조HK-2세포CK화α-SMA양성세포적평균광밀도치。결과배양제3 d,대조조HK-2세포정현포로석양상피세포형태특점,유도조세포정장사형,유사섬유세포,약물조세포이상피세포위주,소수세포정사형;여대조조상비교,유도조CK양성세포평균광밀도치현저강저( P<0.05),α-SMA양성세포평균광밀도치증가(P<0.05);여유도조상비교,약물조CK양성세포평균광밀도치현저증가(P<0.05),α-SMA양성세포평균광밀도치현저강저(P<0.05)。결론①갈조다당류산지구유억제TGF-β1체외유도적신소관상피세포간질전분화적작용;②갈조다당류산지가능통과개변세포골가성분발휘억제신소관상피세포간질전분화작용。
Objective To observe the Fucoidan in vitro against TGF-β1-induced renal tubular epithelial cells ( HK-2 ) mesenchy-mal transition process cytokeratin (cytokeratin,CK) and α-smooth muscle actin (α-smooth muscle action,α-SMA) expression,and to explore the Fucoidan on HK-2 epithelial-mesenchymal transition and its mechanism .Methods We cultured cell lines of normal human renal tubular epithelial cells (HK-2).Using an inverted phase contrast microscope ,we observed morphological changes of cells in con-trol group,induction group and drug group .With the use of immune cells SABC method we cultured HK-2 cells CK andα-SMA-positive cells of the control group ,the induction group and the drug group for 3 days and detected their average optical density values with image analysis .Results After three days of culture ,HK-2 cells showed cobblestone morphology characteristic of epithelial cells in the control group,long fusiform in the induction group ,which was similar to fibroblasts,and mainly epithelial cells over cells in the drug group ,with a few cells fusiform.Compared with the control group ,the average optical density values of CK-positive cells in the induced group were significantly lower (P<0.05),which those of α-SMA-positive cells increased (P<0.05).Compared with the induction group the av-erage optical density values of CK-positive cells in the drug group were significantly incerased ( P<0.05 ) , Wile those of α-SMA-posi-tive cells were significantly lower (P<0.05).Conclusion ①Fucoidan inhibits vitro mesenchymal transdifferentiation of TGF-β1-in-duced renal tubular epithelial cells;②Fucoidan may play a part inhibiting mesenchymal transdifferentiation of renal tubular epithelial cells by altering the cytokeleton .