Novel C-type lectin mediated non-specific cytotoxic cells killing activity through NCCRP-1 in nile tilapia ( Oreochromis niloticus)

被引:0
|
作者
Huang, Yu [1 ,2 ]
Chen, Zhengsi [1 ]
Zhang, Jiaxuan [1 ]
Amoah, Kwaku [1 ]
Asiedu, Berchie [3 ]
Cai, Jia [1 ,2 ]
Wang, Bei [1 ,2 ]
Jian, Jichang [1 ,2 ]
机构
[1] Guangdong Ocean Univ, Coll Fishery, Guangdong Prov Key Lab Aquat Anim Dis Control & Hl, Zhanjiang, Peoples R China
[2] Guangdong Prov Engn Res Ctr Aquat Anim Hlth Assess, Shenzhen, Peoples R China
[3] Univ Energy & Nat Resources, Dept Fisheries & Water Resources, POB 214, Sunyani, Ghana
基金
中国国家自然科学基金;
关键词
CTL; NCCRP-1; Y2H; Nile tilapia; Streptococcus agalactiae; FISH ICTALURUS-PUNCTATUS; MANNOSE-BINDING LECTIN; MOLECULAR-CLONING; RECEPTOR NCCRP-1; EXPRESSION; GENE; IDENTIFICATION; PROTEIN-1; GRANZYMES; TELEOSTS;
D O I
10.1016/j.fsi.2024.109594
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Non-specific cytotoxic cells (NCCs) are vital immune cells involved in teleost's non-specific immunity. As a receptor molecule on the NCCs' surface, the non-specific cytotoxic cell receptor protein 1 (NCCRP-1) is known to play a crucial role in mediating their activity. Nevertheless, there have been limited studies on the signal molecule that transmits signals via NCCRP-1. In this study, a yeast two-hybrid (Y2H) library of tilapia liver and head kidney was constructed and subsequently screened with the bait vector NCCRP-1 of Oreochromis niloticus (On-NCCRP-1) to obtain a C-type lectin (On-CTL) with an interacting protein sequence. Consequently, the fulllength sequence of On-CTL was cloned and analyzed. The expression analysis revealed that On-CTL is highly expressed in the liver and is widely distributed in other tissues. Furthermore, On-CTL expression was significantly up-regulated in the brain, intestine, and head kidney following a challenge with Streptococcus agalactiae. A pointto-point Y2H method was also used to confirm the binding between On-NCCRP-1 and On-CTL. The recombinant On-CTL (rOn-CTL) protein was purified. In vitro experiments demonstrated that rOn-CTL can up-regulate the expression of killer effector molecules in NCCs via its interaction with On-NCCRP-1. Moreover, activation of NCCs by rOn-CTL resulted in a remarkable enhancement in their ability to eliminate fathead minnow cells, indicating that rOn-CTL effectively modulates the killing activity of NCCs through the NCC receptor molecule On-NCCRP-1. These findings significantly contribute to our comprehension of the regulatory mechanisms governing NCC activity, paving the way for future research in this field.
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页数:10
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