Lian J, Chen C S, Fang J J, Chen L W, Cai W C, Zhao G J, Hong G L, Lu Z Q
Emergency Department, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325000, China.
Xiangshan Hospital Affiliated to Wenzhou Medical University, Ningbo 315700, China.
Zhonghua Yi Xue Za Zhi. 2021 Feb 23;101(7):504-510. doi: 10.3760/cma.j.cn112137-20200616-01863.
To investigate the role of Orai1-mediated store-operated calcium entry in the immune damage of CD4 T cells in septic mice. Sepsis mouse model was established by cecal ligation and puncture(CLP). Balb/c mice of clean grade were sacrificed 1, 3, and 5 days after operation. Spleen samples were harvested at given intervals. Splenic CD4 T cells were selected by immunomagnetic beads and the expression of Orai1 protein was detected by western blotting, the storage operated calcium entry (SOCE) was detected by flow cytometry, the apoptosis of CD4 T cells was detected by flow cytometry, the proliferation of CD4 T cells was detected by CCK-8, and the IFN-γ and IL-4 were detected by enzyme-linked immunosorbent assay (ELISA). Then the expression of Orai1 protein was regulated to further detect the SOCE and immune function of splenic CD4 T cells in mice. The experiment was divided into 4 groups, sham group, CLP3 group, Orai1 down group (Orai1-down group) and Orai1 up regulation group (Orai1-up group). The relative expression of Orai1 protein in splenic CD4 T cells in sham group was 1.03±0.16. Compared with sham group, Orai1 protein levels in CLP Group were all significantly lower (19.64, 0.000 5). The increased value of splenic CD4 T cells fluorescence intensity in sham group was 494±41. Compared with sham group, the levels of SOCE in CLP Group were all lower (30.01, 0.001). The ratio of early and late apoptosis of CD4 T cells in sham group was 8.7%±1.5%. Compared with sham group, the early and late apoptosis rates of CLP Group were significantly higher (32.29, 0.000 1). The OD of sham group was 0.81±0.10 at 450 nm. Compared with sham group, the proliferation ability of splenic CD4 T cells in CLP Group were significantly decreased (7.26, 0.001 8). Compared with sham group, the secretion of IFN-γ and IL-4 by CD4 T cells and the ratio of IFN-γ/IL-4 in CLP Group were all significantly decreased (19.690, 6.183, 11.230, all <0.05). Compared with CLP3 group, the increased value of fluorescence intensity of CD4 T cells was significantly decreased, the early and late apoptosis ratio of CD4 T cells was significantly increased, the OD450 nm value of CD4 T cells was decreased, the multiplication capacity of splenic CD4 T cells were decreased, the level of IFN-γ and IL-4 secreted by T cells were decreased, and the value of IFN-γ/IL-4 in orai1-down group was decreased (4.819, 7.952, 2.988, 28.760, 3.140, 7.670, all <0.05). However, Orail-up group showed the opposite trend. Orai1-mediated store-operated calcium entry can alleviate the immune dysfunction of CD4 T cells in septic mice.
探讨Orai1介导的钙库操纵性钙内流在脓毒症小鼠CD4⁺ T细胞免疫损伤中的作用。采用盲肠结扎穿孔术(CLP)建立脓毒症小鼠模型。将清洁级Balb/c小鼠于术后1、3、5天处死,按设定时间点采集脾脏样本。采用免疫磁珠法分选脾CD4⁺ T细胞,蛋白质免疫印迹法检测Orai1蛋白表达,流式细胞术检测钙库操纵性钙内流(SOCE),流式细胞术检测CD4⁺ T细胞凋亡,CCK-8法检测CD4⁺ T细胞增殖,酶联免疫吸附测定(ELISA)法检测IFN-γ和IL-4。然后调节Orai1蛋白表达,进一步检测小鼠脾CD4⁺ T细胞的SOCE及免疫功能。实验分为4组:假手术组、CLP3组、Orai1下调组(Orai1-down组)和Orai1上调组(Orai1-up组)。假手术组脾CD4⁺ T细胞Orai1蛋白相对表达量为1.03±0.16。与假手术组比较,CLP组Orai1蛋白水平均显著降低(19.64,P<0.000 5)。假手术组脾CD4⁺ T细胞荧光强度增加值为494±41。与假手术组比较,CLP组SOCE水平均降低(30.01,P<0.001)。假手术组CD4⁺ T细胞早期及晚期凋亡率为8.7%±1.5%。与假手术组比较,CLP组早期及晚期凋亡率均显著升高(32.29,P<0.000 1)。假手术组450 nm处OD值为0.81±0.10。与假手术组比较,CLP组脾CD4⁺ T细胞增殖能力显著降低(7.26,P<0.001 8)。与假手术组比较,CLP组CD4⁺ T细胞分泌的IFN-γ和IL-4及IFN-γ/IL-4比值均显著降低(19.690、6.183、11.230,均P<0.05)。与CLP3组比较,Orai1-down组CD4⁺ T细胞荧光强度增加值显著降低,CD4⁺ T细胞早期及晚期凋亡率显著升高,CD4⁺ T细胞OD450 nm值降低,脾CD4⁺ T细胞增殖能力降低,T细胞分泌的IFN-γ和IL-4水平降低,IFN-γ/IL-4值降低(4.819、7.952、2.988、28.760、3.140、7.670,均P<0.05)。而Orai1-up组呈现相反趋势。Orai1介导的钙库操纵性钙内流可减轻脓毒症小鼠CD4⁺ T细胞免疫功能障碍。