Cutting Edge: CXCR3 Escapes X Chromosome Inactivation in T Cells during Infection: Potential Implications for Sex Differences in Immune Responses

• Published in: The Journal of immunology (1950) Vol. 203; no. 4; pp. 789 - 794
• Main Authors: Oghumu, Steve, Varikuti, Sanjay, Stock, James C, Volpedo, Greta, Saljoughian, Noushin, Terrazas, Cesar A, Satoskar, Abhay R
• Format: Journal Article
• Language: English
• Published: United States 15.08.2019
• Subjects: Animals; Female; Infections - immunology; Male; Mice; Mice, Mutant Strains; Receptors, CXCR3 - genetics; Receptors, CXCR3 - immunology; Sex Characteristics; T-Lymphocyte Subsets - immunology; Th1 Cells - immunology; X Chromosome Inactivation - immunology
• ISSN: 0022-1767; 1550-6606; 1550-6606
• DOI: 10.4049/jimmunol.1800931

CXCR3, an X-linked gene, is subject to X chromosome inactivation (XCI), but it is unclear whether CXCR3 escapes XCI in immune cells. We determined whether CXCR3 escapes XCI in vivo, evaluated the contribution of allelic CXCR3 expression to the phenotypic properties of T cells during experimental infection with Leishmania, and examined the potential implications to sex differences in immune responses. We used a bicistronic CXCR3 dual-reporter mouse, with each CXCR3 allele linked to a green or red fluorescent reporter without affecting endogenous CXCR3 expression. Our results show that CXCR3 escapes XCI, biallelic CXCR3-expressing T cells produce more CXCR3 protein than monoallelic CXCR3-expressing cells, and biallelic CXCR3-expressing T cells produce more IFN-γ, IL-2, and CD69 compared with T cells that express CXCR3 from one allele during Leishmania mexicana infection. These results demonstrate that XCI escape by CXCR3 potentially contributes to the sex-associated bias observed during infection.