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Morphologic, flow cytometric, functional, and molecular analyses of S100B positive lymphocytes, unique cytotoxic lymphocytes containing S100B protein
Author(s) -
Miki Yukari,
Gion Yuka,
Mukae Yuriko,
Hayashi Atsushi,
Sato Hiaki,
Yoshino Tadashi,
Takahashi Kiyoshi
Publication year - 2013
Publication title -
european journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.904
H-Index - 84
eISSN - 1600-0609
pISSN - 0902-4441
DOI - 10.1111/ejh.12036
Subject(s) - cytotoxic t cell , ctl* , cd8 , cd16 , cd3 , biology , immunology , lymphocyte , stimulation , microbiology and biotechnology , immune system , in vitro , endocrinology , biochemistry
Little is known about the S100B + lymphocytes, which are unique human peripheral blood lymphocytes (PBL) containing the S100B protein. It has recently been shown that S100B is released from various types of S100B + cells and exhibits varied cytokine‐like activities. In this study, we precisely characterized the S100B + lymphocytes of healthy adults with respect to the proportion in the whole PBL, immunophenotypes, function, and their S100B mRNA expression and also evaluated their S100B‐releasing activity upon stimulation. S100B + lymphocytes were detected in all individuals examined, and the proportion of S100B + lymphocytes in the whole PBL ranged from 0.42% to 16.15% (mean, 4.21%). In addition, two subtypes of S100B + lymphocytes, a CTL subtype (CD3 + CD8 + CD16 ‐ ) and a NK subtype (CD3 ‐ CD8 ‐ CD16 + ), were detected. The majority of the CTL subtype of S100B + lymphocytes expressed the αβ‐T‐cell receptor. Surprisingly, S100B mRNA was detected not only in S100B + lymphocytes, but also in every S100B ‐ lymphocytes, although the expression levels of S100B mRNA in S100B ‐ lymphocytes were much lower than those of S100B + lymphocytes. The CTL subtype of S100B + lymphocytes exhibited blastic morphological changes, proliferated and released S100B upon stimulation with phytohemagglutinin. The NK subtype of S100B + lymphocytes exhibited morphological NK activity when cocultivated with NK‐sensitive target, K‐562 cells. Thus, the CTL subtype of S100B + lymphocytes exhibit the biological characteristics of T cells, while the NK subtype of S100B + lymphocytes exhibit the characteristics of NK cells. These results suggest that S100B + lymphocytes are a particular subtype of cytotoxic lymphocytes that play a unique role in antitumor immunity.