4.5 Article

CD5-low expression lymphocytes in canine peripheral blood show characteristics of natural killer cells

期刊

JOURNAL OF LEUKOCYTE BIOLOGY
卷 84, 期 6, 页码 1501-1510

出版社

WILEY
DOI: 10.1189/jlb.0408255

关键词

cytotoxicity; LDH-releasing test; T cell markers

资金

  1. National Science Council [NSC-96-2313-B-002-007]
  2. Council of Agriculture of Taipei, Taiwan [COA 96AS-1.2.1-AD-U1]

向作者/读者索取更多资源

NK cell markers and receptors have been discovered in many mammalian species, such as humans, mice, rats, pigs, and cows. However, there is still a lack of information concerning NK cell markers or receptors in canines. We have discovered that canine CD5-low density (CD5(lo)) cells in PBL are closely associated with NK cell characteristics. CD5(lo) cells comprised 14.9 +/- 6.68% of the total PBL. A high proportion of the CD5(lo) cell population expressed CD3 (96.6%), CD8 alpha (77.7%), CD8 beta (53%), alpha/beta TCR (83%), and CD11/18 (80%), but the expression of gamma/delta TCR (6.5%), CD4 (10.6%), and CD21 (2.4%) was low. CD5(lo) cells were larger than CD5-high density (CD5(hi)) cells. Light and electron microscopy revealed numerous large cytoplasmic granules in CD5(lo) cells, especially after IL-2 stimulation, which was in contrast to CD5hi, in which intracytoplasmic granules were not frequently seen. After IL-2 stimulation, CD5(lo) cells had significantly stronger NK cytotoxicity than CD5(hi) cells. CD5(lo) cells had much higher mRNA levels for NKG2D, CD16, CD94, CD160, perforin, and granzyme than CD5(hi). Following IL-2 stimulation, CD5(lo) cells had significantly higher mRNA levels of NKp30, NKp44, CD16, and CD94 than CD5(hi) cells. In addition, IL-2-stimulated, CD5(lo)-depleted PBL showed a loss of NK cytotoxicity. CD5(lo) cells also showed significantly lower antigen-specific cytotoxic T cell activity as compared with CD5(hi) cells. Taken together, the CD5(lo) subset in canine PBL is closely related to canine NK cells, and CD5(lo) can be used as a phenotypic marker for an IL-2-dependent canine NK cell enrichment. J. Leukoc. Biol. 84: 1501-1510; 2008.

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