College of Life Science, Liaoning Normal University, Dalian 116081, China.
Lamprey Research Center, Liaoning Normal University, Dalian 116081, China.
Int J Mol Sci. 2017 Sep 22;18(10):2035. doi: 10.3390/ijms18102035.
Vav guanine nucleotide exchange factor 3 (Vav3), a Rho family GTPase, regulates multiple cell signaling pathways including those of T- and B-cell receptors in vertebrates through mediating the activities of the Rho family members. Whether the lamprey possesses Vav3 homolog and what role it plays in immune response remain unknown. Gene cloning, recombinant expression, antibody production and expression pattern analyses were performed to characterize the lamprey Vav3 in the current study. The lamprey Vav3 is closer to jawed vertebrates' Vav3 molecules (about 53% identities in general) than to Vav2 molecules of jawless and jawed vertebrates (about 51% identities in general) in sequence similarity. Conserved motif analysis showed that the most distinguished parts between Vav3 and Vav2 proteins are their two Src-homology 3 domains. The relative expression levels of lamprey mRNA and protein were significantly up-regulated in lamprey lymphocytes and supraneural myeloid bodies after mixed-antigens stimulation, respectively. In addition, lamprey Vav3 were up-regulated drastically in lymphocytes and supraneural myeloid bodies after lipopolysaccharide (LPS) rather than phytohemagglutinin (PHA) stimulation. Lamprey Vav3 distributed in the cytoplasm of variable lymphocyte receptor B positive (VLRB⁺) lymphocytes, and the number of plasmacytes (VLRB and lamprey Vav3 double positive) in blood lymphocytes also increased after LPS stimulation. Our results proved that lamprey Vav3 was involved in the LPS-mediated immune reaction of lamprey and provided a clue for the further study of the precise role lamprey Vav3 played in the signaling pathway of lamprey VLRB⁺ lymphocytes.
Vav 鸟嘌呤核苷酸交换因子 3(Vav3)是一种 Rho 家族 GTPase,通过调节 Rho 家族成员的活性,调节脊椎动物 T 细胞和 B 细胞受体等多种细胞信号通路。文昌鱼是否具有 Vav3 同源物及其在免疫反应中的作用尚不清楚。本研究通过基因克隆、重组表达、抗体生产和表达模式分析,对文昌鱼 Vav3 进行了鉴定。文昌鱼 Vav3 与有颌脊椎动物的 Vav3 分子(总体约 53%的同一性)比与无颌和有颌脊椎动物的 Vav2 分子(总体约 51%的同一性)在序列相似性上更接近。保守基序分析表明,Vav3 和 Vav2 蛋白之间最显著的区别是它们的两个Src 同源性 3 结构域。混合抗原刺激后,文昌鱼淋巴细胞和神经上髓样体中 mRNA 和蛋白的相对表达水平均显著上调。此外,脂多糖(LPS)而非植物血凝素(PHA)刺激后,文昌鱼淋巴细胞和神经上髓样体中 Vav3 明显上调。文昌鱼 Vav3 分布在可变淋巴细胞受体 B 阳性(VLRB⁺)淋巴细胞的细胞质中,LPS 刺激后血液淋巴细胞中的浆细胞(VLRB 和文昌鱼 Vav3 双阳性)数量也增加。我们的结果证明,文昌鱼 Vav3 参与了 LPS 介导的文昌鱼免疫反应,为进一步研究文昌鱼 Vav3 在 VLRB⁺淋巴细胞信号通路中的精确作用提供了线索。