Mice lacking all of the Skint family genes. (26th April 2018)

• Record Type: Journal Article
• Authors: Narita, Tomoya; Nitta, Takeshi; Nitta, Sachiko; Okamura, Tadashi; Takayanagi, Hiroshi
• Is Part Of: International immunology. Volume 30:Number 7(2018)
• Page Start: 301
• Page End: 309
• Publication Date: 2018-04-26
• Subjects: CRISPR/Cas9 -- development -- Skint family -- γδT cell -- Vγ5Vδ1; Immunology -- Periodicals; 616.079
• DOI: 10.1093/intimm/dxy030
• Languages: English
• ISSNs: 0953-8178

Abstract

Abstract : Skint-family genes only regulate one subset of γδT cells Abstract: γδT cells develop in the thymus and play important roles in protection against infection and tumor development, but the mechanisms by which the thymic microenvironment supports γδT cell differentiation remain largely unclear. Skint1, a B7-related protein expressed in thymic epithelial cells, was shown to be essential for the development of mouse Vγ5Vδ1 γδT cells. The Skint family in mouse consists of 11 members, Skint1-11. Here we generated mutant mice lacking the entire genomic region that contains all of the Skint genes. These mice exhibited a marked reduction of Vγ5Vδ1 γδT cells in the thymus and skin, but surprisingly, had normal development of other γδT cell subsets and leukocytes including αβT, B and myeloid cells. This phenotype is essentially identical to that of Skint1 -deficient mice. These results indicate that the Skint family exerts an exclusive function in regulating the development of Vγ5Vδ1 γδT cells and is dispensable for development of other leukocytes.