The inflammatory action of CD 40 ligand ( CD 154 ) expressed on activated human platelets is temporally limited by coexpressed CD 40

Recently, we have demonstrated that human platelets carry preformed CD40 ligand (CD154) molecules, which rapidly appear on the platelet surface following stimulation by thrombin. Once on the surface, platelet CD154 induces an inflammatory reaction of CD40-bearing endothelial cells. This study shows that strong platelet agonists other than thrombin also lead to the expression of CD154 on the platelet surface. At the same time, several lines of evidence are presented that together indicate that thrombotic events in the vasculature are generally accompanied by activation of the inflammatory potential of platelet CD154. This study also reports the constitutive expression of CD40, the receptor for CD154, on platelets. The binding of CD154 to coexpressed CD40 in the platelet aggregate leads within minutes to hours to the cleavage of membrane-bound surface CD154 and the release of an 18-kd soluble form of the molecule. Soluble CD154 (sCD154), in contrast to transmembrane CD154, can no longer induce an inflammatory reaction of endothelial cells. These findings indicate that the interaction of platelet CD154 with CD40 on neighboring cells is temporally limited to prevent an uncontrolled inflammation at the site of thrombus formation. Thus, similar to the very tight regulation of the CD154-CD40 interaction in the immune system, an effective mechanism controls the inflammatory potential of platelet CD154 in the vascular system. (Blood. 2001;98:1047-1054)

[1]  M. Daemen,et al.  Requirement for CD154 in the progression of atherosclerosis , 1999, Nature Medicine.

[2]  L. Rassenti,et al.  The soluble CD40 ligand sCD154 in systemic lupus erythematosus. , 1999, The Journal of clinical investigation.

[3]  W. Fanslow,et al.  Incorporation of an Isoleucine Zipper Motif Enhances the Biological Activity of Soluble CD40L (CD154)* , 1999, The Journal of Biological Chemistry.

[4]  P. Presek,et al.  Secreted ADP Plays a Central Role in Thrombin-induced Phospholipase D Activation in Human Platelets , 1998, Thrombosis and Haemostasis.

[5]  P. Doherty,et al.  Thymic lymphoproliferative disease after successful correction of CD40 ligand deficiency by gene transfer in mice , 1998, Nature Medicine.

[6]  Reinhold Förster,et al.  CD40 ligand on activated platelets triggers an inflammatory reaction of endothelial cells , 1998, Nature.

[7]  P. Morateck,et al.  A dinucleotide deletion results in defective membrane anchoring and circulating soluble glycoprotein Ib alpha in a novel form of Bernard-Soulier syndrome. , 1997, Blood.

[8]  H. Haugen,et al.  Thymus dysfunction and chronic inflammatory disease in gp39 transgenic mice. , 1997, International immunology.

[9]  R. Geha,et al.  Exogenous CD40 ligand induces a pulmonary inflammation response. , 1997, Journal of immunology.

[10]  H. Haugen,et al.  Thymic Overexpression of CD40 Ligand Disrupts Normal Thymic Epithelial Organization , 1997, The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society.

[11]  B. Ludewig,et al.  Induction, regulation, and function of soluble TRAP (CD40 ligand) during interaction of primary CD4+ CD45RA+ T cells with dendritic cells , 1996, European journal of immunology.

[12]  J. Suttles,et al.  The many roles of CD40 in cell-mediated inflammatory responses. , 1996, Immunology today.

[13]  P. Kiener,et al.  Activation of human monocytes through CD40 induces matrix metalloproteinases. , 1996, Journal of immunology.

[14]  A. Matsushima,et al.  Functional interactions of T cells with endothelial cells: the role of CD40L-CD40-mediated signals , 1995, The Journal of experimental medicine.

[15]  George Kollias,et al.  The transmembrane form of tumor necrosis factor is the prime activating ligand of the 80 kDa tumor necrosis factor receptor , 1995, Cell.

[16]  P. Kiener,et al.  Stimulation of CD40 with purified soluble gp39 induces proinflammatory responses in human monocytes. , 1995, Journal of immunology.

[17]  A. Greinacher,et al.  Platelet phospholipase D is activated by protein kinase C via an integrin alpha IIb beta 3-independent mechanism. , 1995, The Biochemical journal.

[18]  S. Fortune,et al.  Ligation of CD40 on fibroblasts induces CD54 (ICAM‐1) and CD106 (VCAM‐1) up‐regulation and IL‐6 production and proliferation , 1995, Journal of leukocyte biology.

[19]  P. Kiener,et al.  Expression of functional CD40 by vascular endothelial cells , 1995, The Journal of experimental medicine.

[20]  R. Kroczek,et al.  A soluble form of TRAP (CD40 ligand) is rapidly released after T cell activation , 1995, European journal of immunology.

[21]  K. Enssle,et al.  Monomeric and dimeric forms of soluble receptors can differ in their neutralization potential. , 1995, Behring Institute Mitteilungen.

[22]  J. Pober,et al.  CD40 on human endothelial cells: inducibility by cytokines and functional regulation of adhesion molecule expression. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[23]  L. Notarangelo,et al.  Defective Expression of CD40 Ligand on T Cells Causes “X‐Linked Immunodeficiency with Hyper‐IgM (HIGM1)” , 1994, Immunological reviews.

[24]  G. Inghirami,et al.  CD40 molecules induce down-modulation and endocytosis of T cell surface T cell-B cell activating molecule/CD40-L. Potential role in regulating helper effector function. , 1994, Journal of immunology.

[25]  L. Notarangelo,et al.  Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM , 1993, Nature.

[26]  H. Mages,et al.  Cloning of TRAP, a ligand for CD40 on human T cells , 1992, European journal of immunology.

[27]  E. Clark,et al.  Molecular and biological characterization of a murine ligand for CD40 , 1992, Nature.

[28]  S. Lederman,et al.  Identification of a novel surface protein on activated CD4+ T cells that induces contact-dependent B cell differentiation (help) , 1992, The Journal of experimental medicine.

[29]  G. Schieven,et al.  Stimulation of protein tyrosine phosphorylation, phosphoinositide turnover, and multiple previously unidentified serine/threonine-specific protein kinases by the Pan-B-cell receptor CD40/Bp50 at discrete developmental stages of human B-cell ontogeny. , 1991, The Journal of biological chemistry.

[30]  J. Banchereau,et al.  Activation of human B lymphocytes through CD40 and interleukin 4 , 1989, European journal of immunology.

[31]  E. Clark,et al.  Activation of human B cells mediated through two distinct cell surface differentiation antigens, Bp35 and Bp50. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[32]  E. Jaffe,et al.  Culture of human endothelial cells derived from umbilical veins. Identification by morphologic and immunologic criteria. , 1973, The Journal of clinical investigation.

[33]  J. Banchereau,et al.  CD40-CD40 ligand: a multifunctional receptor-ligand pair. , 1996, Advances in immunology.

[34]  J. Mustard,et al.  Isolation of human platelets from plasma by centrifugation and washing. , 1989, Methods in enzymology.