TY - JOUR
T1 - Characterization of murine CD160+ CD8+ T lymphocytes
AU - Tsujimura, Kunio
AU - Obata, Yuichi
AU - Matsudaira, Yasue
AU - Nishida, Keiko
AU - Akatsuka, Yoshiki
AU - Ito, Yoshinori
AU - Demachi-Okamura, Ayako
AU - Kuzushima, Kiyotaka
AU - Takahashi, Toshitada
N1 - Funding Information:
This work was supported by grants from the Japan Society for the Promotion of Science, the Ministry of Education, Culture, Sports, Science and Technology, and the Ministry of Health, Labour and Welfare, Japan. We thank Ms. H. Tamaki and Dr. M.A. Moore for their expert assistance.
PY - 2006/7/15
Y1 - 2006/7/15
N2 - CD160 is an Ig-like glycoprotein expressed on NK, NKT and TCRγδ T cells, as well as intestinal intraepithelial T lymphocytes. In addition, a minor subset of CD8+ but not CD4+ T cells in the periphery is also known to express CD160, but the subset has not been fully characterized. In this study, we prepared anti-murine CD160 mAbs and investigated the expression profile of CD160 on various subsets of CD8+ T cells. The amount of CD160 on almost all CD8+ T cells was increased upon CD3-mediated stimulation in vitro, and soluble CD160 was found to be released. Flow cytometric analysis revealed most CD8+ T cells expressing CD160 to show a CD44high phenotype in vivo. On further analysis, both CD44highCD62Llow effector memory T cells (TEM) and CD44highCD62Lhigh central memory T cells (TCM) expressed CD160 at an intermediate level. High levels were evident with recently activated CD8+ TEM. Naïve CD8+ T cells presumably immediately after stimulation (CD44lowCD62LlowCD69+) also expressed CD160, but only at a low level. Purified CD160+ CD8+ T cells from OT-1 transgenic mice expressing TCR against OVA residues 257-264 presented by H-2Kb produced IFN-γ more rapidly than CD160- CD8+ T cells upon antigen stimulation. These results together show that CD160 is expressed on the majority of CD8+ memory T cells as well as recently activated CD8+ T cells.
AB - CD160 is an Ig-like glycoprotein expressed on NK, NKT and TCRγδ T cells, as well as intestinal intraepithelial T lymphocytes. In addition, a minor subset of CD8+ but not CD4+ T cells in the periphery is also known to express CD160, but the subset has not been fully characterized. In this study, we prepared anti-murine CD160 mAbs and investigated the expression profile of CD160 on various subsets of CD8+ T cells. The amount of CD160 on almost all CD8+ T cells was increased upon CD3-mediated stimulation in vitro, and soluble CD160 was found to be released. Flow cytometric analysis revealed most CD8+ T cells expressing CD160 to show a CD44high phenotype in vivo. On further analysis, both CD44highCD62Llow effector memory T cells (TEM) and CD44highCD62Lhigh central memory T cells (TCM) expressed CD160 at an intermediate level. High levels were evident with recently activated CD8+ TEM. Naïve CD8+ T cells presumably immediately after stimulation (CD44lowCD62LlowCD69+) also expressed CD160, but only at a low level. Purified CD160+ CD8+ T cells from OT-1 transgenic mice expressing TCR against OVA residues 257-264 presented by H-2Kb produced IFN-γ more rapidly than CD160- CD8+ T cells upon antigen stimulation. These results together show that CD160 is expressed on the majority of CD8+ memory T cells as well as recently activated CD8+ T cells.
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U2 - 10.1016/j.imlet.2006.04.006
DO - 10.1016/j.imlet.2006.04.006
M3 - Article
C2 - 16764942
AN - SCOPUS:33746242383
SN - 0165-2478
VL - 106
SP - 48
EP - 56
JO - Immunology Letters
JF - Immunology Letters
IS - 1
ER -