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作 者:李青[1] 吕林莉[1] 郑敏[1] 马坤岭[1] 张晓良[1] 刘必成[1]
机构地区:[1]东南大学附属中大医院肾脏科东南大学肾脏病研究所,南京210009
出 处:《中华肾脏病杂志》2011年第11期825-830,共6页Chinese Journal of Nephrology
基 金:国家自然科学基金(81130010);江苏省自然科学基金(BK2011061);江苏省高校研究生科研创新计划(cx09B_065Z)
摘 要:目的观察单核细胞(U937细胞)对人近端肾小管上皮细胞(HK-2细胞)转分化的影响及其分子机制。方法将HK-2细胞与人单核细胞系U937细胞共培养;倒置相差显微镜观察HK-2细胞形态;Western印迹、实时荧光定量PCR法检测仅平滑肌肌动蛋白(α-SMA)、纤连蛋白(FN)、E钙黏蛋白(E—cadherin)和胞间黏附分子1(ICAM-1)表达;BCECF—AM荧光染色法测定单核细胞黏附;流式细胞仪法检测HK-2细胞表面分子ICAM-1表达;基因芯片筛选HK-2细胞基因变化;利用信号阻断剂阻断基因芯片筛选出的信号通路,进一步验证单核细胞诱导肾小管上皮细胞转分化的分子机制。结果单核细胞可直接诱导HK-2细胞发生形态变化,减少HK-2细胞E-cadherin表达(均P〈0.05),并上调α-SMA、FN表达(均P〈0.05)。应用CD18抗体阻断CD18-ICAM-1可抑制单核细胞黏附及其诱导的HK-2细胞形态变化。基因芯片结果显示,NF—κB信号通路分子CC亚族趋化因子配体20(CCL20)、白细胞介素(IL)2、IL-8、脂磷壁酸(LTA)及血小板内皮细胞黏附分子1(PECAMl)表达明显增加(均P〈0.05)。NF—KB信号阻断剂吡咯烷二硫氨基甲酸(PDTC)能显著抑制HK-2细胞形态变化及表面ICAM-1表达,抑制单核细胞诱导的肾小管上皮细胞转分化。结论单核细胞通过CD18分子与HK-2细胞表面ICAM-1结合,从而启动NF—κB信号通路介导的特定基因转录,最终导致肾小管上皮细胞发生转分化。Objective To investigate the effects of monocytes on phenotypic changes of human proximal tubular HK-2 cells and the mechanism. Methods Monocytes were co-cuhured with HK-2 cells. Morphological changes of HK-2 cells were detected by inverted phase contrast microscope. Expressions of E-cadherin, α-SMA and fibronectin were assessed by RT-PCR, Western blotting and immunocytochemical staining. Flow cytometry techniques was applied to evaluate intercellular cell adhesion molecule-1 (ICAM-1) expression on HK-2 cells. The intracellular signal was investigated by gene microarray. Results The typical epithelial cell morphology of HK-2 cells disappeared after co-culture with monocytes, accompanied by decreased E-cadherin expression and increased α-SMA and fibronectin expression (all P〈0.05). The expression of ICAM-1 on HK-2 cells was increased by monocytes stimulation. Interestingly, administration of CD18 antibody directly inhibited the phenotypic change of HK-2 cells. Furthermore, NF-κB signaling might be critical in mediating this process, and blockade of this signaling pathway could inhibit ICAM-1 expression and epithelial mesenchymal transition (EMT) formation. Conclusion Monocytes can directly induce EMT of HK-2 cells via up-regulating ICAM-1 through NF-κB signaling pathway.
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