Yang Yang, Wang Wen-Sheng, Qiu Yuan, Sun Li-Hua, Yang Hua
Department of General Surgery, Xinqiao Hospital, The Third Military Medical University, Chongqing 400037, China.
Zhonghua Wei Chang Wai Ke Za Zhi. 2013 May;16(5):479-83.
To investigate the role of cyclic adenosine monophosphate(cAMP) in the regulation of intestinal epithelial barrier function under hypoxia.
Intestinal epithelial barrier was established by Caco-2 monolayers. Cells were divided into four groups: normoxia (Nx), normoxia plus Forskolin(Nx+FSK), hypoxia(Hx), hypoxia plus SQ22536(Hx+SQ22536). cAMP concentrations of different groups were assessed by cAMP enzyme immunoassay kit. RT-PCR and Western blotting were used to detect the mRNA and protein expressions of claudin-1 and occludin under normoxic and hypoxic condition. Caco-2 monolayers were grown on Millicell filters, and transepithelial electrical resistance(TER) was measured using a Millipore electric resistance system.
The concentration of cAMP under hypoxic conditions(Hx group) was higher compared with Nx group [(6.30±0.50) pmol/L vs. (2.38±0.18) pmol/L, P<0.01]. At the same time, both mRNA and protein expressions of claudin-1 and occluding were lower in Hx group than those in Nx group(all P<0.05). TER decreased by 76.30±0.64(P<0.01). When the monolayers were exposed to hypoxia plus SQ22536 (Hx+SQ22536 group), the concentration of cAMP was(2.12±0.23) pmol/L, which was lower than that under hypoxic conditions(Hx group, P<0.01). Both mRNA and protein expressions of claudin-1 and occludin were higher compared to Hx group (all P<0.01). TER increased by 32.96±2.16 (P<0.05).
When Caco-2 cells are exposed to hypoxia, barrier function, claudin-1 and occludin expression are diminished in parallel with a high level of intracellular cAMP compared with the normoxic condition. Inhibition of the intracellular cAMP level under hypoxia can maintain the intestinal epithelial function through regulating the claudin-1 and occludin expression and attenuate the permeability of intestinal mucosa.
探讨环磷酸腺苷(cAMP)在缺氧状态下对肠上皮屏障功能调节中的作用。
采用Caco-2单层细胞建立肠上皮屏障。细胞分为四组:常氧组(Nx)、常氧加福斯高林组(Nx+FSK)、缺氧组(Hx)、缺氧加SQ22536组(Hx+SQ22536)。采用cAMP酶免疫分析试剂盒检测不同组的cAMP浓度。运用RT-PCR和蛋白质印迹法检测常氧和缺氧条件下claudin-1和闭合蛋白的mRNA及蛋白表达。Caco-2单层细胞生长于密理博滤膜上,使用密理博电阻系统测量跨上皮电阻(TER)。
缺氧条件下(Hx组)的cAMP浓度高于常氧组[(6.30±0.50)pmol/L对(2.38±0.18)pmol/L,P<0.01]。同时,Hx组claudin-1和闭合蛋白的mRNA及蛋白表达均低于Nx组(均P<0.05)。TER下降了76.30±0.64(P<0.01)。当单层细胞暴露于缺氧加SQ22536(Hx+SQ22536组)时,cAMP浓度为(2.12±0.23)pmol/L,低于缺氧条件下(Hx组,P<0.01)。与Hx组相比,claudin-1和闭合蛋白的mRNA及蛋白表达均升高(均P<0.01)。TER升高了32.96±2.16(P<0.05)。
当Caco-2细胞暴露于缺氧环境时,与常氧条件相比,屏障功能、claudin-1和闭合蛋白表达降低,同时细胞内cAMP水平升高。缺氧状态下抑制细胞内cAMP水平可通过调节claudin-1和闭合蛋白表达维持肠上皮功能,并减轻肠黏膜通透性。