State Key Laboratory of Estuarine and Coastal Research, Laboratory of Aquatic Comparative Immunology, School of Life Sciences, East China Normal University, Shanghai, 200241, China.
State Key Laboratory of Estuarine and Coastal Research, Laboratory of Aquatic Comparative Immunology, School of Life Sciences, East China Normal University, Shanghai, 200241, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.
Fish Shellfish Immunol. 2019 Jun;89:281-289. doi: 10.1016/j.fsi.2019.04.003. Epub 2019 Apr 3.
H-Ras is a guanosine triphosphatase (GTPase), which acts as a molecular switch and controls multiple important cellular processes including lymphocyte activation and function. However, regulatory mechanism of adaptive immune response by H-Ras remains unclear in non-mammalian animals. In the present study, we investigated the involvement of H-Ras in lymphocyte activation with a teleost model Oreochromis niloticus. H-Ras from O. niloticus (On-H-Ras) is highly conserved with those from other vertebrates. The mRNA of On-H-Ras showed a wide expression pattern in the lymphoid-tissues and with the highest level in liver. After Aeromonas hydrophila infection, transcription of On-H-Ras was significantly induced on day 8 but came back to basal level on day 16, suggesting that On-H-Ras potentially participated in primary response during the adaptive immunity. Furthermore, On-H-Ras mRNA was obviously up-regulated when leukocytes were activated by T lymphocyte mitogen PHA in vitro. Meanwhile, protein level of H-Ras was also augmented once leukocytes were stimulated with lymphocyte receptor signaling agonist PMA and ionomycin. More importantly, once Ras activity was inhibited by specific inhibitor, the up-regulation of lymphocyte activation marker CD122 was obviously impaired during lymphocyte activation process. Therefore, On-H-Ras regulated lymphocyte activation through both mRNA and protein level. Altogether, our results illustrated the involvement of H-Ras in teleost adaptive immunity via controlling lymphocyte activation, and thus provided a novel perspective to understand evolution of the lymphocyte-mediated adaptive immunity.
H-Ras 是一种鸟嘌呤三磷酸酶(GTPase),作为分子开关,控制着包括淋巴细胞激活和功能在内的多种重要细胞过程。然而,H-Ras 在非哺乳动物动物中的适应性免疫反应的调节机制尚不清楚。在本研究中,我们以硬骨鱼模型奥利亚罗非鱼(Oreochromis niloticus)研究了 H-Ras 在淋巴细胞激活中的作用。奥利亚罗非鱼的 H-Ras(On-H-Ras)与其他脊椎动物的 H-Ras 高度保守。On-H-Ras 的 mRNA 在淋巴组织中有广泛的表达模式,在肝脏中的表达水平最高。在感染嗜水气单胞菌后,On-H-Ras 的转录在第 8 天显著诱导,但在第 16 天恢复到基础水平,表明 On-H-Ras 可能在适应性免疫的原发性反应中发挥作用。此外,当白细胞在体外被 T 淋巴细胞有丝分裂原 PHA 激活时,On-H-Ras mRNA 明显上调。同时,当白细胞被淋巴细胞受体信号激动剂 PMA 和离子霉素刺激时,H-Ras 蛋白水平也增加。更重要的是,一旦 Ras 活性被特异性抑制剂抑制,在淋巴细胞激活过程中,淋巴细胞激活标志物 CD122 的上调明显受损。因此,On-H-Ras 通过 mRNA 和蛋白水平调节淋巴细胞的激活。总之,我们的结果表明,H-Ras 通过控制淋巴细胞的激活参与了硬骨鱼的适应性免疫,从而为理解淋巴细胞介导的适应性免疫的进化提供了新的视角。