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. Author manuscript; available in PMC: 2013 Sep 13.
Published in final edited form as: Nature. 2008 Nov 2;457(7230):722–725. doi: 10.1038/nature07537

Figure 2. A subset of tonsil NKp44+ NK cells express CCR6, respond to CCL20 in vitro and in vivo, produce CCL20, and adhere to epithelial cells.

Figure 2

a, Approximately 50% of NKp44+ NK cells express CCR6. b, Tonsil NK cells migrate in response to CCL20. Bars indicate the ratio between the percentage of input NKp44+ NK cells versus the percentage of migrated NKp44+ NK cells. c, PMA/ionomycin treated NKp44+ NK cells produce significantly more CCL20 than NKp44 NK cells. d, e, A case of dermatitis with pathological LC accumulation shows extensive skin infiltration of NKp44+ NK cells as compared to a normal skin. Arrows indicate pseudo-Pautrier abscesses indicative of LC accumulation6. f, Real time PCR shows that skin with LC accumulation produces more CCL20 than normal skin. g, NKp44+ NK cells express higher levels of CD96 than NKp44 NK cells. h, A discrete subset of NKp44+ NK cells expresses CD103. i, NKp44+ NK cells firmly adhere to epithelial cells. The ratio of NKp44+ to NKp44 cells within non-adherent and adherent CD3CD56+ cells was determined by flow cytometry. j, The adhesiveness of NKp44+ NK cells to epithelial cells is consistent in different donors. All error bars indicate s.d. with n=3