Chen Huahui, Lv Miao, Lv Zhimeng, Li Chenghua, Xu Wei, Zhang Weiwei, Zhao Xuelin, Duan Xuemei, Jin Chunhua
School of Marine Sciences, Ningbo University, PR China.
School of Marine Sciences, Ningbo University, PR China.
Fish Shellfish Immunol. 2017 Jan;60:447-457. doi: 10.1016/j.fsi.2016.11.033. Epub 2016 Nov 12.
Cathepsin B (CTSB), a member of lysosomal cysteine protease, is involved in multiple levels of physiological and biological processes, and also plays crucial roles in host immune defense against pathogen infection in vertebrates. However, the function of CTSB within the innate immune system of invertebrates, particularly in marine echinoderms, has been poorly documented. In this study, the immune function of CTSB in Apostichopus japonicus (designated as AjCTSB), a commercially important and disease vulnerable aquaculture specie, was investigated by integrated molecular and protein approaches. A 2153 bp cDNA representing the full-length of AjCTSB was cloned via overlapping ESTs and RACE fragments. AjCTSB contained an open reading frame of 999 bp encoding a secreted protein of 332 amino acid residues with a predicted molecular mass of 36.8 kDa. The deduced amino acid of AjCTSB shared a typical activity center containing three conserved amino acid residues (Cys, His and Asn). Phylogenetic tree analysis also supported that AjCTSB was a new member of CTSB family with clustering firstly with invertebrate CTSBs. Quantitative real time PCR analysis revealed that AjCTSB was ubiquitously expressed in all examined tissues with the highest levels in intestine. The Vibrio splendidus challenged sea cucumber and LPS-exposed coelomocytes could both significantly boost the expression of AjCTSB. Moreover, the purified recombinant AjCTSB exhibited dose-dependent CTSB activities at the concentration ranged from 0 to 0.24 μg μL. Further functional analysis indicated that coelomocytes apoptosis was significantly inhibited by 0.16-fold in vivo and the apoptosis execution Ajcaspase 3 was extremely reduced in Apostichopus japonicus coelomocytes treated with specific AjCTSB siRNA. Collectively, all these results suggested that AjCTSB was an important immune factor and might be served as apoptosis enhancers in pathogen challenged sea cucumber.
组织蛋白酶B(CTSB)是溶酶体半胱氨酸蛋白酶家族的成员,参与多个层面的生理和生物学过程,在脊椎动物宿主抵御病原体感染的免疫防御中也发挥着关键作用。然而,CTSB在无脊椎动物,特别是海洋棘皮动物的先天免疫系统中的功能,目前记录较少。在本研究中,通过整合分子和蛋白质方法,对重要的商业养殖且易患病的刺参(Apostichopus japonicus)中CTSB(命名为AjCTSB)的免疫功能进行了研究。通过重叠的EST和RACE片段克隆得到了一个2153 bp的cDNA,代表AjCTSB的全长。AjCTSB包含一个999 bp的开放阅读框,编码一个由332个氨基酸残基组成的分泌蛋白,预测分子量为36.8 kDa。AjCTSB推导的氨基酸序列具有一个典型的活性中心,包含三个保守的氨基酸残基(半胱氨酸、组氨酸和天冬酰胺)。系统发育树分析也支持AjCTSB是CTSB家族的一个新成员,首先与无脊椎动物的CTSB聚类。定量实时PCR分析表明,AjCTSB在所有检测组织中均有广泛表达,在肠道中表达水平最高。灿烂弧菌攻击的海参和暴露于LPS的体腔细胞均可显著提高AjCTSB的表达。此外,纯化的重组AjCTSB在0至0.24 μg μL的浓度范围内表现出剂量依赖性的CTSB活性。进一步的功能分析表明,体内体腔细胞凋亡被显著抑制了0.16倍,在用特异性AjCTSB siRNA处理的刺参体腔细胞中,凋亡执行蛋白Ajcaspase 3极度减少。总的来说,所有这些结果表明AjCTSB是一种重要的免疫因子,在病原体攻击的海参中可能作为凋亡增强剂发挥作用。