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Published on: April 16, 2015
Expression of IL-2 receptor p55 and p75 chains by human B lymphocytes: effects of activation and differentiation
H Zola1, H Weedon, G R Thompson
1Department of Clinical Immunology, Flinders Medical Centre, Bedford Park, South Australia.
Insights
Human B cells express interleukin-2 receptor (IL-2R) chains upon activation. While blood B cells show expression, tonsil B cells require culture and protein synthesis for low-level IL-2R p55 chain detection.
Area of Science:
- Immunology
- Cell Biology
Background:
- Interleukin-2 receptor (IL-2R) is crucial for T cell proliferation and function.
- Expression of IL-2R on B cells is less understood compared to T cells.
Purpose of the Study:
- To investigate the expression of IL-2R p55 and p75 chains on human B cells.
- To determine the modulation of IL-2R expression by B cell activation factors.
Main Methods:
- High-sensitivity immunofluorescence was used to detect IL-2R expression.
- Tonsil B cells were cultured with various B cell activators.
- Flow cytometry was employed to analyze cell surface marker expression.
Main Results:
- Fresh tonsil B cells showed no detectable IL-2R expression.
- Cultured tonsil B cells exhibited low-level p55 chain expression, dependent on protein synthesis.
- IL-4, IL-2, and TNF-beta modulated p55 levels, while IL-5 did not.
- IL-2R expression changes were minor compared to CD23 activation marker.
- T-cell blasts showed the most significant p55 expression upon polyclonal stimulation.
Conclusions:
- Human B cells can express IL-2R, particularly the p55 chain, upon activation in vitro.
- IL-2R expression on B cells is influenced by specific cytokines and activation signals.
- IL-2R expression on B cells is generally low and less pronounced than on activated T cells.
Abstract:
Whilst B cells in human blood can be shown to express interleukin-2 receptor (IL-2R) p55 and p75 chains, using a high-sensitivity immunofluorescence procedure, fresh tonsil B cells did not show detectable levels of expression. Culture of tonsil B cells led to low levels of expression of the p55 chain of the IL-2R, an effect which was dependent on protein synthesis. The level of expression of IL-2R chains could be modulated by culturing in the presence of a number of factors which activate B cells. p55 levels were more readily modulated than p75 levels. IL-4 and combinations of IL-4 with anti-IgM, IL-2 or tumour necrosis factor-beta (TNF-beta) modulated p55 levels, but IL-5 did not. Changes in IL-2R expression were small when compared with other B-cell activation markers such as CD23. When unfractionated tonsil cells were activated with a polyclonal stimulus, the major change was the expression of p55 by T-cell blasts--p75 expression remained low in T and B cells, and p55 expression by B cells remained low.
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