Lv Zhimeng, Zhang Zhen, Wei Zhixin, Li Chenghua, Shao Yina, Zhang Weiwei, Zhao Xuelin, Xiong Jinbo
School of Marine Sciences, Ningbo University, Ningbo 315211, PR China.
School of Marine Sciences, Ningbo University, Ningbo 315211, PR China.
Dev Comp Immunol. 2017 Dec;77:128-137. doi: 10.1016/j.dci.2017.07.026. Epub 2017 Aug 1.
High mobility group box protein 3 (HMGB3) regulates proliferation and inflammatory response in vertebrates. However, its functional roles in invertebrates are largely unknown. In this study, a HMGB3 homologue molecule was identified from Apostichopus japonicus (designated as AjHMGB3) by RACE approach. The full-length cDNA of AjHMGB3 was of 2298 bp with an open reading frame of 1320 bp encoding a 439-amino-acid (aa) residue protein. Structural analysis then conducted and the results revealed that AjHMGB3 processed two conserved HMGBs (133-204 and 210-279 aa) and an acidic tail. The results of subsequent multiple sequence alignment and phylogenetic analysis both indicated that AjHMGB3 belongs to a new member of HMGB3 protein subfamily. Furthermore, AjHMGB3 was expressed in all examined tissues except in tentacles and particularly highly expressed in the intestine, as indicated by spatial expression analysis results. The Vibrio splendidus challenge in vivo and lipolysaccharide (LPS) stimulation in vitro can significantly upregulate the mRNA expression of AjHMGB3 in coelomocytes. This finding is consistent with the expression profiles of TLR cascade members. We further investigated the expression profiles of AjMyD88 and Ajp105 after the gain- or loss-of-function of AjHMGB3 in coelomocytes. The results showed that AjMyD88 and Ajp105 were upregulated 2.19- and 2.83-fold in AjHMGB3 overexpressed treatment and downregulated 0.38- and 0.43-fold in the AjHMGB3 silencing group. The p50 subunit displayed expression profiles that are identical to those of AjMyD88 and Ajp105 according to the Western blot results. In the same condition, the respiratory burst was increased by 37.5% in the AjHMGB3 overexpressed group and depressed by 28.2% in the AjHMGB3 knock-down group. Our present findings collectively suggested that AjHMGB3 acted as an NF-κB activator and produced ROS production in sea cucumbers.
高迁移率族蛋白B3(HMGB3)调节脊椎动物的增殖和炎症反应。然而,其在无脊椎动物中的功能作用 largely unknown。在本研究中,通过RACE方法从刺参中鉴定出一种HMGB3同源分子(命名为AjHMGB3)。AjHMGB3的全长cDNA为2298 bp,开放阅读框为1320 bp,编码一个439个氨基酸(aa)残基的蛋白质。随后进行了结构分析,结果显示AjHMGB3具有两个保守的HMGB结构域(133 - 204和210 - 279 aa)和一个酸性尾巴。随后的多序列比对和系统发育分析结果均表明AjHMGB3属于HMGB3蛋白亚家族的一个新成员。此外,空间表达分析结果表明,AjHMGB3在除触手外的所有检测组织中均有表达,在肠道中表达尤为高。体内灿烂弧菌攻击和体外脂多糖(LPS)刺激均可显著上调体腔细胞中AjHMGB3的mRNA表达。这一发现与TLR级联成员的表达谱一致。我们进一步研究了体腔细胞中AjHMGB3功能获得或丧失后AjMyD88和Ajp105的表达谱。结果显示,在AjHMGB3过表达处理中,AjMyD88和Ajp105分别上调了2.19倍和2.83倍,而在AjHMGB3沉默组中分别下调了0.38倍和0.43倍。根据蛋白质印迹结果,p50亚基的表达谱与AjMyD88和Ajp105相同。在相同条件下,AjHMGB3过表达组的呼吸爆发增加了37.5%,而AjHMGB3敲低组则降低了28.2%。我们目前的研究结果共同表明,AjHMGB3在海参中作为NF-κB激活剂并产生ROS。