School of Marine Sciences, Ningbo University, Ningbo, 315211, PR China.
School of Marine Sciences, Ningbo University, Ningbo, 315211, PR China.
Fish Shellfish Immunol. 2019 Apr;87:839-846. doi: 10.1016/j.fsi.2019.02.040. Epub 2019 Feb 20.
Macrophage migration inhibitory factor (MIF) is a cytokine and plays critical roles in inflammatory and immune responses in vertebrates. However, its functional role in inflammation has not been well studied in invertebrates. In the present study, we cloned and characterized MIF gene from Apostichopus japonicus by RNA-seq and RACE approaches (designated as AjMIF). A 1047 bp fragment representing the full-length cDNA of AjMIF was obtained, including a 5' UTR of 100 bp, an open reading frame (ORF) of 366 bp encoding a polypeptide of 121 amino acids residues with the molecular weight of 13.43 kDa and theoretical isoelectric point of 5.63 and a 3' UTR of 580 bp. SMART analysis showed that AjMIF has conserved MIF domain (2-117aa) similar to its mammalian counterparts. The amino terminal proline residue (P) and invariant lysine residue (K) which are critical active sites of tautomerase activity in mammalian MIF were also detected. Phylogenic analysis and multiple alignments have shown that AjMIF shared higher degree of structural conservation and sequence identities with other counterparts from invertebrates and vertebrates. For Vibrio splendidus challenged sea cucumber, the peak expression of AjMIF mRNAs in coelomocytes were detected at 6 h (23.5-fold) and remained at high levels until 24 h (4.01-fold), and returned to normal level at 48 h in comparison with that of the control group. Similarly, a significant increase in the relative mRNA levels of AjMIF was also found in 10 μg mL LPS-exposed primary cultured coelomocytes. Functional analysis indicated that recombinant AjMIF incubation could promote inflammatory response related genes of Ajp105, AjVEGF, AjMMP1 and AjHMGB3 expression by 1.35-fold, 1.36-fold, 1.83-fold and 1.27-fold increase, respectively, which was consistent with the findings in vertebrate MIFs. All these results collectively suggested that AjMIF had a similar function to MIFs in higher animals and might serve as a candidate cytokine in inflammatory regulation in sea cucumber.
巨噬细胞移动抑制因子(MIF)是一种细胞因子,在脊椎动物的炎症和免疫反应中发挥着关键作用。然而,它在无脊椎动物炎症中的功能作用尚未得到很好的研究。在本研究中,我们通过 RNA-seq 和 RACE 方法从刺参(Apostichopus japonicus)中克隆和鉴定了 MIF 基因(命名为 AjMIF)。获得了一个代表 AjMIF 全长 cDNA 的 1047bp 片段,包括 100bp 的 5'UTR、366bp 的开放阅读框(ORF),编码一个由 121 个氨基酸残基组成的多肽,分子量为 13.43kDa,理论等电点为 5.63,3'UTR 为 580bp。SMART 分析表明,AjMIF 具有保守的 MIF 结构域(2-117aa),与哺乳动物的 MIF 相似。在哺乳动物 MIF 中,具有异构酶活性的关键活性位点脯氨酸残基(P)和不变的赖氨酸残基(K)也被检测到。系统发育分析和多重比对表明,AjMIF 与无脊椎动物和脊椎动物的其他同源物具有更高程度的结构保守性和序列同一性。在刺参受到灿烂弧菌(Vibrio splendidus)攻击时,在体腔细胞中检测到 AjMIF mRNAs 的峰值表达在 6 小时(23.5 倍),并保持高水平直至 24 小时(4.01 倍),与对照组相比,在 48 小时时恢复正常水平。同样,在 10μg/mL LPS 暴露的原代培养体腔细胞中,AjMIF 的相对 mRNA 水平也显著增加。功能分析表明,重组 AjMIF 孵育可使 Ajp105、AjVEGF、AjMMP1 和 AjHMGB3 等炎症反应相关基因的表达分别增加 1.35 倍、1.36 倍、1.83 倍和 1.27 倍,与脊椎动物 MIFs 的发现一致。所有这些结果共同表明,AjMIF 在高等动物中的功能与 MIFs 相似,可能是刺参炎症调节的候选细胞因子。