Interaction with Autologous Platelets Multiplies Interleukin-l and Tumor Necrosis Factor Production in Mononuclear Cells
Author(s) -
Koichi Aiura,
Burton D. Clark,
Charles A. Dinarello,
Nathan Margolis,
G. Kaplanski,
John F. Burke,
Ronald G. Tompkins,
Jeffrey A. Gelfand
Publication year - 1997
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1093/infdis/175.1.123
Subject(s) - platelet , peripheral blood mononuclear cell , tumor necrosis factor alpha , immunology , lipopolysaccharide , cytokine , interleukin , medicine , chemistry , in vitro , biochemistry
The effect of activated platelets on cytokine production by human peripheral blood mononuclear cells (PBMC) was investigated. When PBMC were coincubated with activated autologous platelets amid lipopolysaccharide (LPS, 50-100 pg/mL) for 8 h, the production of interleukin (IL)-1alpha increased 11- to 18-fold and tumor necrosis factor (TNF)-alpha 3- to 5-fold compared with PBMC without platelets. Activated platelets in a dual-chamber well that prevented platelet-PBMC contact but permitted passage of soluble factors enhanced IL-1alpha production (P < .01). Platelet-PBMC contact in the chamber resulted in a further enhancement of IL-1alpha production. These data suggest that platelet-PBMC interaction, both directly and with platelet-derived factors, enhances production of shock-producing IL-1alpha and TNF-alpha, albeit differently. The interaction of platelets with monocytes may play an important role in the pathophysiology of sepsis and disseminated intravascular coagulation.
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