Literature DB >> 9716456

L-selectin stimulates the neutral sphingomyelinase and induces release of ceramide.

B Brenner1, H U Grassmé, C Müller, F Lang, C P Speer, E Gulbins.   

Abstract

Selectins have been shown to be crucial in the rolling process of leukocytes during lymphocyte homing and in the early phase of inflammatory processes. Recently, we and others have shown that binding of L-selectin to its ligands correlates with a rapid induction of several intracellular signaling molecules, in particular, Src-like tyrosine kinases, MAP-kinases, Jun NH2-terminal kinase, the small G-proteins Ras and Rac, and a release of Ca2+ in leukocytes. Here, we demonstrate the activation of a novel signaling pathway by L-selectin. Stimulation of Jurkat T-lymphocytes via L-selectin results in an increase of neutral sphingomyelinase activity. This activity correlates with a consumption of cellular sphingomyelin and a release of ceramide. The activation of the neutral sphingomyelinase by L-selectin does not depend on tyrosine kinase activity and, therefore, represents an alternative and novel pathway to stimulate lymphocytes via L-selectin. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9716456     DOI: 10.1006/excr.1998.4146

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   3.905


  2 in total

1.  Costimulation of T-cell proliferation by anti-L-selectin antibody is associated with the reduction of a cdk inhibitor p27.

Authors:  Ken-Ichi Nishijima; Munetoshi Ando; Shusuke Sano; Aiko Hayashi-Ozawa; Yoshinori Kinoshita; Shinji Iijima
Journal:  Immunology       Date:  2005-11       Impact factor: 7.397

Review 2.  A head-to-tail view of L-selectin and its impact on neutrophil behaviour.

Authors:  Aleksandar Ivetic
Journal:  Cell Tissue Res       Date:  2018-01-20       Impact factor: 5.249

  2 in total

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