Lysozyme as a regulator of interleukin-2-activated lymphocyte proliferation

N Yabe1, K Komiya, T Takezono

  • 1Department of Hygiene, Dokkyo University School of Medicine, Tochigi, Japan.

Insights

Lysozyme

Area of Science:

  • Immunology
  • Cell Biology

Background:

  • Lysozyme is an enzyme with known antimicrobial properties.
  • Its role in modulating lymphocyte proliferation is not fully understood.

Purpose of the Study:

  • To investigate the dual effect of lysozyme on interleukin-2 (IL-2)-stimulated human peripheral blood lymphocyte proliferation.
  • To identify factors influencing lysozyme's augmentation or inhibition of lymphocyte response.

Main Methods:

  • Human peripheral blood lymphocytes were stimulated with varying concentrations of IL-2.
  • Lysozyme was added at different time points and concentrations.
  • Lymphocyte proliferation was assessed under conditions with and without serum and with varying lymphocyte activation states.

Main Results:

  • Lysozyme augmented IL-2-mediated proliferation at suboptimal IL-2 concentrations.
  • Lymphocyte activation with anti-CD3 antibody shifted augmentation to inhibition.
  • Eliminating MHC class II+ cells enhanced lysozyme's augmenting effect.
  • Early lysozyme addition (within 1 hour) promoted proliferation, while later addition was inhibitory.
  • Serum presence modulated lysozyme's effect, often retarding its action.

Conclusions:

  • Lysozyme exhibits context-dependent regulation of lymphocyte proliferation.
  • Its effects are influenced by IL-2 levels, lymphocyte activation, timing of addition, and serum presence.
  • Lysozyme may play a role in fine-tuning immune responses based on stimulus magnitude and cellular events.

Related Concept Videos

The JAK-STAT Signaling Pathway01:20

The JAK-STAT Signaling Pathway

Several cytokine receptors have tightly bound Janus kinase or JAK proteins attached at their cytosolic tail. Small signaling molecules such as cytokines, growth hormones, or prolactins bind to the cytokine receptors and initiate their dimerization. The dimerization brings the cytosolic JAKs together that trans-phosphorylate and activates each other. The activated JAKs now phosphorylate cytosolic tails of the cytokine receptors, which serve as binding sites for adaptor proteins such as  SH2...
Inflammatory Response01:28

Inflammatory Response

An inflammatory response is a localized, nonspecific immune reaction that occurs when a tissue is injured. It is characterized by redness, swelling, heat, and pain, which are commonly called the cardinal signs and symptoms of inflammation. Inflammation can sometimes result in a loss of function.
Inflammation can be triggered by various stimuli, such as impact, abrasion, chemical irritation, infections, and extreme hot or cold temperatures. These can damage cells and connective tissue fibers,...
T Cell Types and Functions01:24

T Cell Types and Functions

When T cells with CD4 markers are activated, they give rise to two types of effector cells: helper T cells and regulatory T cells. Meanwhile, T cells with CD8 markers differentiate into effector cytotoxic T cells. The differentiation of CD4 T cells into helper T cell subsets, such as Th1, Th2, and Th17 cells, is dependent on the antigen type, antigen-presenting cell, and regulatory cytokines.
Th1 cells stimulate dendritic cells to express necessary co-stimulatory molecules on their surfaces for...
B Cell Activation and Differentiation01:24

B Cell Activation and Differentiation

The adaptive immune response, a sophisticated defense mechanism, relies on the activation and differentiation of B lymphocytes, or B cells. These processes enable our bodies to mount a tailored response against specific pathogens such as bacteria, free virus particles, toxins, and parasites.
When naive B cells encounter a specific antigen that can bind to the B cell receptor (BCR) on their surface, they undergo sensitization to respond to the antigen's presence. Sensitization begins with...