z-logo
Premium
Sinomenine inhibits primary CD4 + T‐cell proliferation via apoptosis
Author(s) -
Shu Luan,
Yin Wu,
Zhang Jing,
Tang Bo,
Kang YuanXi,
Ding Fan,
Hua ZiChun
Publication year - 2007
Publication title -
cell biology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.932
H-Index - 77
eISSN - 1095-8355
pISSN - 1065-6995
DOI - 10.1016/j.cellbi.2007.01.035
Subject(s) - sinomenine , apoptosis , chemistry , microbiology and biotechnology , t cell , immune system , population , biology , immunology , pharmacology , biochemistry , medicine , environmental health
Sinomenine is an active component isolated from Sinomenium acutum and is widely used as an immunosuppressive drug for treating autoimmune diseases. CD4 + T‐cell population plays a key role in adaptive immune response and is related to some autoimmune diseases. In this study, we investigated the possible immunosuppressive effect of sinomenine on CD4 + T cells and its underlying mechanism. Our data demonstrated that sinomenine remarkably suppressed the proliferation of CD4 + T cells, blocked the cell cycle progression from G0/G1 phase to S plusG2/M phases. Finally, the immunosuppressive activity elicited by sinomenine in CD4 + primary lymphocytes was found to be largely accounted for by caspase 3‐dependent cells apoptosis. Sinomenine did not significantly alter the expression of bcl‐2 in activated CD4 + primary T cells, suggesting that bcl‐2 might not be involved in sinomenine‐induced T cells apoptosis. In sum, this study proposes a novel mechanism for the immunosuppressive function of sinomenine on primary mouse CD4 + T cells.

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