The lectin jacalin induces phosphorylation of ERK and JNK in CD4 + T cells

Seetha M. Lakshmi Tamma, V. S. Kalyanaraman, Savita Pahwa, Paul Dominguez, Ron R. Modesto

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25 Scopus citations

Abstract

The CD4 molecule plays an essential role in mediating the transduction of intracellular signals by functioning as a coreceptor for the complex T cell receptor/CD3 and also acts as the primary receptor for human immunodeficiency virus (HIV). Several authors have shown evidence that jacalin, a plant lectin, binds to CD4 and inhibits in vitro HIV infection. We analyzed jacalin-induced intracellular signaling events in CD4+ T cells and have shown that cell activation resulted in tyrosine phosphorylation of intracellular substrates p56lck, p59fyn, ZAP-70, p95vav, phospholipase C-γ1, and ras activation, as assessed by conversion of ras guanosine 5′-diphosphate to ras guanosine 5′-triphosphate. We further examined extracellular regulated kinase (ERK) and c-jun NH2-terminal kinase (JNK) phosphorylation following stimulation with jacalin. The data indicate that the kinetics of JNK phosphorylation is delayed. Optimum phosphorylation of ERK2 was observed by 10 min, and that of JNK was observed by 30 min. Pretreatment with gp120 followed by stimulation with jacalin resulted in marked inhibition of all of the aforementioned intracellular events. The data presented here provide insight into the intracellular signaling events associated with the CD4 molecule-jacalin-gp120 interactions and HIV-induced CD4+ T cell anergy. Jacalin may be used as a possible tool for the study of CD4-mediated signal transduction and HIV-impaired CD4+ T cell activation.

Original languageEnglish (US)
Pages (from-to)682-688
Number of pages7
JournalJournal of Leukocyte Biology
Volume73
Issue number5
DOIs
StatePublished - May 1 2003

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Keywords

  • PLC-γ1
  • RAS
  • Vav

ASJC Scopus subject areas

  • Cell Biology

Cite this

Lakshmi Tamma, S. M., Kalyanaraman, V. S., Pahwa, S., Dominguez, P., & Modesto, R. R. (2003). The lectin jacalin induces phosphorylation of ERK and JNK in CD4 + T cells. Journal of Leukocyte Biology, 73(5), 682-688. https://doi.org/10.1189/jlb.1102534