CXCR3.1 and CXCR3.2 Differentially Contribute to Macrophage Polarization in Teleost Fish.

J Immunol

Laboratory of Biochemistry and Molecular Biology, Ningbo University, Ningbo 315211, People's Republic of China

Published: June 2017

AI Article Synopsis

  • * It was found that these isoforms play different roles in macrophage polarization, with CXCR3.1 linked to an M1 phenotype (pro-inflammatory) and CXCR3.2 associated with an M2 phenotype (anti-inflammatory) in species like ayu and grass carp.
  • * The research indicates that specific proteins and transcription factors are involved in this polarization process, and improved outcomes were observed in septic ayu with PaCXCR3.2 macrophages, highlighting the importance of these genes in immune responses.

Article Abstract

The study of multiple copies of chemokine receptor genes in various teleosts has long appealed to investigators seeking to understand the evolution of the immune system. The CXCR CXCR3 gene has two isoforms, CXCR3.1 and CXCR3.2, which are both expressed in macrophages. The distinct roles of teleost CXCR3s have not been identified previously. In this article, we found that CXCR3.1 and CXCR3.2 differentially contributed to macrophage polarization in the teleosts: ayu (), grass carp (), and spotted green pufferfish (). In ayu macrophages, the CXCR3.1 (PaCXCR3.1) gene was constitutively expressed, whereas the CXCR3.2 (PaCXCR3.2) gene was induced postinfection with Upon infection, PaCXCR3.1 and PaCXCR3.2 macrophages showed an M1 and an M2 phenotype, respectively. CXCL9-11-like proteins mediated M1 and M2 polarization by interacting with the PaCXCR3.1 and PaCXCR3.2 proteins on macrophages, respectively. The transcription factors STAT1 and STAT3 were activated in PaCXCR3.1 and PaCXCR3.2 macrophages, respectively. Furthermore, the prognosis of septic ayu adoptively transferred with PaCXCR3.2 macrophages was improved. Our data reveal a previously unknown mechanism for macrophage polarization, suggesting that redundant genes may regulate crucial functions in the teleost immune system.

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Source
http://dx.doi.org/10.4049/jimmunol.1700101DOI Listing

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