Morphologic, flow cytometric, functional, and molecular analyses of S100B positive lymphocytes, unique cytotoxic

Yukari Miki1, Yuka Gion, Yuriko Mukae

  • 1Department of Medical Technology, Graduate School of Health Sciences, Okayama University, Okayama, Japan.

Insights

Unique S100B⁺ lymphocytes, found in human blood, were characterized. These cells, including T and NK cell subtypes, release S100B and may play a role in antitumor immunity.

Area of Science:

  • Immunology
  • Cell Biology
  • Human Physiology

Background:

  • S100B protein is released by various cells and exhibits cytokine-like activities.
  • S100B⁺ lymphocytes are unique peripheral blood lymphocytes (PBL) containing S100B protein, but their characteristics are largely unknown.
  • Understanding S100B⁺ lymphocytes is crucial for insights into immune responses and potential therapeutic targets.

Purpose of the Study:

  • To precisely characterize S100B⁺ lymphocytes in healthy adults.
  • To determine their proportion in PBL, immunophenotypes, function, and S100B mRNA expression.
  • To evaluate their S100B-releasing activity upon stimulation.

Main Methods:

  • Flow cytometry for immunophenotyping of S100B⁺ lymphocytes.
  • Analysis of S100B mRNA expression using molecular techniques.
  • Functional assays including proliferation and cytotoxic activity assessments upon stimulation.

Main Results:

  • S100B⁺ lymphocytes were detected in all individuals, ranging from 0.42% to 16.15% of PBL.
  • Two subtypes were identified: a CTL subtype (CD3⁺ CD8⁺ CD16⁻) and an NK subtype (CD3⁻ CD3⁻ CD16⁺).
  • Both subtypes expressed S100B mRNA, with higher levels in S100B⁺ lymphocytes compared to S100B⁻ lymphocytes. CTL subtypes proliferated and released S100B upon stimulation, while NK subtypes showed NK activity.

Conclusions:

  • S100B⁺ lymphocytes represent a distinct subtype of cytotoxic lymphocytes.
  • The CTL and NK subtypes exhibit characteristics of T cells and NK cells, respectively.
  • These findings suggest a unique role for S100B⁺ lymphocytes in antitumor immunity.