z-logo
Premium
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.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom