Vδ1+ T cells are crucial for repertoire formation of γδ T cells in the lung

Biochemical and Biophysical Research Communications

Volumn 365, Issue 2, 2008, Pages 246-251

  Li, Shigen ^a   Kishihara, Kenji ^a   Akashi, Nobuko ^a   Hara, Hiromitsu ^b   Yoshikai, Yasunobu ^c   Maekawa, Yoichi ^a   Yasutomo, Koji ^a  

^a UNIVERSITY OF TOKUSHIMA   (Japan)

^b SAGA UNIVERSITY   (Japan)

^c KYUSHU UNIVERSITY   (Japan)

Author keywords

T cells; Cell development and differentiation; Knockout mice; Lung; Resdent pulmonary T cell; T cell receptors

Indexed keywords

T LYMPHOCYTE RECEPTOR; LYMPHOCYTE ANTIGEN RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL COUNT; CELL MIGRATION; COMPARATIVE STUDY; CONTROLLED STUDY; FETUS; GENE EXPRESSION; LUNG; LUNG ALVEOLUS EPITHELIUM; MICROENVIRONMENT; MOUSE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; T LYMPHOCYTE; WILD TYPE; ANIMAL; C57BL MOUSE; CELL COMMUNICATION; CELL CULTURE; CELL DIFFERENTIATION; CYTOLOGY; METABOLISM; MOUSE MUTANT; PHYSIOLOGY;

MUS;

ANIMALS; CELL COMMUNICATION; CELL DIFFERENTIATION; CELLS, CULTURED; LUNG; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; RECEPTORS, ANTIGEN, T-CELL, GAMMA-DELTA; T-LYMPHOCYTES;

EID: 36248970762     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.10.163     Document Type: Article

References (18)

1. Penninger J., Wallace V.A., Kishihara K., Molina T., Krause H., and Mak T.W. Molecular organization, ontogeny and expression of murine αβ and γδ T cell receptors. Exp. Clin. Immunogenet. 8 (1991) 57-74
2. Haas W., Pereira P., and Tonegawa S. γδ T cells. Annu. Rev. Immunol. 11 (1993) 637-685
3. Xiong N., and Raulet D.H. Development and selection of γδ T cells. Immunol. Rev. 215 (2007) 15-31
4. Born W.K., Lahn M., Takeda K., Kanehiro A., O'Brien R.L., and Gelfand E.W. Role of γδ T cells in protecting normal airway function. Respir. Res. 1 (2000) 151-158
5. Arden B., Clark P.S., Kabelitz D., and Mak T.W. Mouse T-cell receptor variable gene segment families 42 (1995) 501-530
6. Ito K., Bonneville M., Takagaki Y., Nakanishi N., Kanagawa O., Krecko E.G., and Tonegawa S. Different γδ T-cell receptors are expressed on thymocytes at different stages of development. Proc. Natl. Acad. Sci. USA 86 (1989) 631-635
7. Itohara S., Farr A.G., Lafaille J.J., Bonneville M., Takagaki Y., Haas W., and Tonegawa S. Homing of a γδ thymocyte subset with homogeneous T-cell receptors to mucosal epithelia. Nature 343 (1990) 754-757
8. Augustin A., Kubo R.T., and Sim G.K. Resident pulmonary lymphocytes expressing the γδ T-cell receptor. Nature 340 (1989) 239-241
9. Sim G.K., Rajaserkar R., Dessing M., and Augustin A. Homing and in situ differentiation of resident pulmonary lymphocytes. Int. Immunol. 6 (1994) 1287-1295
10. Hara H., Kishihara K., Matsuzaki G., Takimoto H., Tsukiyama T., Tigelaar R.E., and Nomoto K. Development of dendritic epidermal T cells with a skewed diversity of γδ TCRs in Vδ1-deficient mice. J. Immunol. 165 (2000) 3695-3705
11. Pereira P., Gerber D., Huang S.Y., and Tonegawa S. Ontogenic development and tissue distribution of Vγ1-expressing γδ T lymphocytes in normal mice. J. Exp. Med. 182 (1995) 1921-1930
12. Fujise S., Kishihara K., Lee K.Y., Matsuzaki G., and Nomoto K. Normal macrophage functions, but impaired induction of γδ T cells, at the site of bacterial infection in CD45 exon6-deficient mice. Eur. J. Immunol. 27 (1997) 2549-2556
13. + γδ T cells elicited by inflammation. J. Leuc. Biol. 75 (2004) 68-75
14. Weber-Arden J., Wilbert O.M., Kabelitz D., and Arden B. Vδ repertoire during thymic ontogeny suggests three novel waves of γδ TCR expression. J. Immunol. 164 (2000) 1002-1012
15. Mallick-Wood C.A., Lewis J.M., Richie L.I., Owen M.J., Tigelaar R.E., and Hayday A.C. Conservation of T cell receptor conformation in epidermal γδ cells with disrupted primary Vγ gene usage. Science 279 (1998) 1729-1733
16. + γδ T cells producing CC chemokines may bridge a gap between neutrophils and macrophages in innate immunity during Escherichia coli infection in mice. J. Immunol. 173 (2004) 5156-5164
17. + γδ T cells control early infiltration of neutrophils after Escherichia coli infection via IL-17 production. J. Immunol. 178 (2007) 4466-4472
18. Wands J.M., Roark C.L., Aydintug M.K., Jin N., Hahn Y.S., Cook L., Yin X., Dal Porto J., Lahn M., Hyde D.M., Gelfand E.W., Mason R.J., O'BrieL R.L., and Born W.K. Distribution and leukocyte contacts of γδ T cells in the lung. J. Leuk. Biol. 78 (2005) 1086-1096