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Grillot, D.A., Merino, R., Pena, J.C., Fanslow, W.C., Finkelman, F.D., Thompson, C.B. and Nunez, G. (1996) Bcl-X Exhibits Regulated Expression during B Cell Development and Activation and Modulates Lymphocyte Survival in Transgenic Mice. Journal of Experimental Medicine, 183, 381-391.
http://dx.doi.org/10.1084/jem.183.2.381

has been cited by the following article:

• TITLE: Inhibition of T Cell and Stimulation of B Cell Proliferation by Restraint Stress Mediated by Voltage-Gated Potassium Channel 1.3 Expression

  AUTHORS: Juan Feng, Shiqiang Wang, Demao Song

  KEYWORDS: Restraint Stress, Kv1.3, Proliferation, T/B Cell

  JOURNAL NAME: American Journal of Molecular Biology, Vol.5 No.3, July 22, 2015

  ABSTRACT: Our previous study has showed that restraint stress inhibits T cell proliferation. Kv1.3 plays a key role in the lymphocyte activation process. Here, we investigate the effects of restraint stress on murine splenic T and B cell proliferation and the role of Kv1.3 in the process. 3H-TdR incorporation is used to determine changes in splenocyte proliferation stimulated by Con A or LPS between control and restraint stress groups. The data shows that restraint stress inhibits T cell and enhanced B cell proliferation. Data from RT-PCR and Western blotting shows that Kv1.3 gene and protein levels are downregulated in T cells and upregulated in B cells in stressed mice. To examine a possible cause-and-effect relationship between Kv1.3 and stress-affected lymphocyte proliferation, we employ various Kv1.3 specific blockers (quinine, 4-AP and TEA) to determine K+ channel function under restraint stress. The data shows that Kv1.3 blockers reverse the decreased T cell proliferation and increase B cell proliferation induced by restraint stress. These results indicate that Kv1.3 mediates restraint stress-induced modulation of T/B lymphocyte proliferation.