Luo Xing, Chen Ting, Zhong Ming, Jiang Xiao, Zhang Lvping, Ren Chunhua, Hu Chaoqun
CAS Key Laboratory of Tropical Marine Bio-resources and Ecology (LMB), Guangdong Provincial Key Laboratory of Applied Marine Biology (LAMB), South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China; University of Chinese Academy of Sciences, Beijing, China.
CAS Key Laboratory of Tropical Marine Bio-resources and Ecology (LMB), Guangdong Provincial Key Laboratory of Applied Marine Biology (LAMB), South China Sea Institute of Oceanology, Chinese Academy of Sciences, Guangzhou, China.
Peptides. 2015 Jun;68:58-63. doi: 10.1016/j.peptides.2014.11.002. Epub 2014 Nov 15.
Molt-inhibiting hormone (MIH), a peptide member of the crustacean hyperglycemic hormone (CHH) family, is commonly considered as a negative regulator during the molt cycle in crustaceans. Phylogenetic analysis of CHH family peptides in penaeidae shrimps suggested that there is no significant differentiation between MIH and vitellogenesis-inhibiting hormone (VIH, another peptide member of CHH family), by far the most potent negative regulator of crustacean vitellogenesis known. Thus, MIH may also play a role in regulating vitellogenesis. In this study, two previously reported putative MIHs (LivMIH1 and LivMIH2) in the Pacific white shrimp (Litopenaeus vannamei) were expressed in Escherichia coli, purified by immobilized metal ion affinity chromatography (IMAC) and further confirmed by western blot. Regulation of vitellogenin (VTG) mRNA expression by recombinant LivMIH1 and LivMIH2 challenge was performed by both in vitro hepatopancreatic primary cells culture and in vivo injection approaches. In in vitro primary culture of shrimp hepatopancreatic cells, only LivMIH2 but not LivMIH1 administration could improve the mRNA expression of VTG. In in vivo injection experiments, similarly, only LivMIH2 but not LivMIH1 could stimulate hepatopancreatic VTG gene expression and induce ovary maturation. Our study may provide evidence for one isoform of MIH (MIH2 in L. vannamei) may serve as one of the mediators of the physiological progress of molting and vitellogenesis. Our study may also give new insight in CHH family peptides regulating reproduction in crustaceans, in particular penaeidae shrimps.
蜕皮抑制激素(MIH)是甲壳类高血糖激素(CHH)家族的一种肽类成员,通常被认为是甲壳类动物蜕皮周期中的负调节因子。对对虾科虾类CHH家族肽的系统发育分析表明,MIH与卵黄发生抑制激素(VIH,CHH家族的另一种肽类成员,是目前已知的最有效的甲壳类动物卵黄发生负调节因子)之间没有显著差异。因此,MIH可能也在调节卵黄发生中发挥作用。在本研究中,太平洋白对虾(凡纳滨对虾)中两个先前报道的假定MIH(LivMIH1和LivMIH2)在大肠杆菌中表达,通过固定化金属离子亲和色谱(IMAC)纯化,并通过蛋白质免疫印迹进一步确认。通过体外肝胰腺原代细胞培养和体内注射方法,研究重组LivMIH1和LivMIH2刺激对卵黄蛋白原(VTG)mRNA表达的调控。在对虾肝胰腺细胞的体外原代培养中,只有LivMIH2而不是LivMIH1的处理能够提高VTG的mRNA表达。在体内注射实验中,同样只有LivMIH2而不是LivMIH1能够刺激肝胰腺VTG基因表达并诱导卵巢成熟。我们的研究可能为一种MIH同工型(凡纳滨对虾中的MIH2)可能作为蜕皮和卵黄发生生理过程的介质之一提供证据。我们的研究也可能为CHH家族肽调节甲壳类动物,特别是对虾科虾类的繁殖提供新的见解。