离子霉素
免疫系统
淋巴细胞
川地69
脂多糖
CD8型
免疫学
细胞生物学
刺激
佛波
化学
T淋巴细胞
离体
生物
T细胞
体外
内分泌学
信号转导
生物化学
白细胞介素2受体
蛋白激酶C
作者
Mhd Yousuf Yassouf,Xu Zhang,Zisheng Huang,Da Zhai,Reiko Sekiya,Tsuyoshi Kawabata,Tao‐Sheng Li
摘要
Abstract Mechanical forces can modulate the immune response, mostly described as promoting the activation of immune cells, but the role and mechanism of pathological levels of mechanical stress in lymphocyte activation have not been focused on before. By an ex vivo experimental approach, we observed that mechanical stressing of murine spleen lymphocytes with 50 mmHg for 3 h induced the nuclear localization of NFAT1, increased C‐Jun, and increased the expression of early activation marker CD69 in resting CD8+ cells. Interestingly, 50 mmHg mechanical stressing induced the nuclear localization of NFAT1; but conversely decreased C‐Jun and inhibited the expression of CD69 in lymphocytes under lipopolysaccharide or phorbol 12‐myristate 13‐acetate/ionomycin stimulation. Additionally, we observed similar changes trends when comparing RNA‐seq data of hypertensive and normotensive COVID‐19 patients. Our results indicate a biphasic effect of mechanical stress on lymphocyte activation, which provides insight into the variety of immune responses in pathologies involving elevated mechanical stress.
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