Functional characterization of the turkey macrophage migration inhibitory factor

被引:3
作者
Park, Myeongseon [1 ]
Kim, Sungwon [1 ,2 ,3 ]
Fetterer, Raymond H. [4 ]
Dalloul, Rami A. [1 ]
机构
[1] Virginia Tech, Dept Anim & Poultry Sci, Avian Immunobiol Lab, Blacksburg, VA 24061 USA
[2] Univ Edinburgh, Roslin Inst, Easter Bush EH25 9RG, Midlothian, Scotland
[3] Univ Edinburgh, R D SVS, Easter Bush EH25 9RG, Midlothian, Scotland
[4] ARS, Anim Parasit Dis Lab, USDA, Beltsville, MD 20705 USA
关键词
Macrophage migration inhibitory factor; Turkey; Chemotaxis; Cytokines; HIGH SEQUENCE IDENTITY; FACTOR MIF; CRYSTAL-STRUCTURE; IMMUNE-RESPONSE; SECONDARY STRUCTURE; MOLECULAR-CLONING; GENE-EXPRESSION; REGULATORY ROLE; IN-VITRO; CHICKEN;
D O I
10.1016/j.dci.2016.04.005
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Macrophage migration inhibitory factor (MIF) is a soluble protein that inhibits the random migration of macrophages and plays a pivotal immunoregulatory function in innate and adaptive immunity. The aim of this study was to clone the turkey MIF (TkMIF) gene, express the active protein, and characterize its basic function. The full-length TkMIF gene was amplified from total RNA extracted from turkey spleen, followed by cloning into a prokaryotic (pET11a) expression vector. Sequence analysis revealed that TkMIF consists of 115 amino acids with 12.5 kDa molecular weight. Multiple sequence alignment revealed 100%, 65%, 95% and 92% identity with chicken, duck, eagle and zebra finch MIFs, respectively. Recombinant TkMIF (rTkMIF) was expressed in Escherichia coli and purified through HPLC and endotoxin removal. SDS-PAGE analysis revealed an approximately 13.5 kDa of rTkMIF monomer containing T7 tag in soluble form. Western blot analysis showed that anti-chicken MIF (ChMIF) polyclonal antisera detected a monomer form of TkMIF at approximately 13.5 kDa size. Further functional analysis revealed that rTkMIF inhibits migration of both mononuclear cells and splenocytes in a dose-dependent manner, but was abolished by the addition of anti-ChMIF polyclonal antisera. qRT-PCR analysis revealed elevated transcripts of pro inflammatory cytokines by rTkMIF in LPS-stimulated monocytes. rTkMIF also led to increased levels of IFN-gamma and IL-17F transcripts in Con A-activated splenocytes, while IL-10 and IL-13 transcripts were decreased. Overall, the sequences of both the turkey and chicken MIF have high similarity and comparable biological functions with respect to migration inhibitory activities of macrophages and enhancement of pro-inflammatory cytokine expression, suggesting that turkey and chicken MIFs would be biologically cross-reactive. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:198 / 207
页数:10
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