Adherence of human monocytes to haemodialysis membranes: LFA 1 (CDlla/CD18) CR1 (CD35) and CR3 (CDllb/CD18) triggering promotes the biosynthesis of platelet-activating factor and adherence

C. Tetta, F. Tropea, G. Camussi, R. Neri, L. Wratten, L. Sereni, L. Silvestro, C. Franceschi, N. Haeffner-Cavaillon

Research output: Contribution to journalArticle

11 Citations (Scopus)

Abstract

Background Platelet-activating factor is a mediator of inflammation involved in the blood-membrane interaction.We report that selective stimulation of complement receptors (CR1 and CR3) triggers PAF synthesis and monocyte adherenceto complement-activating membranes. Methods The synthesis of PAF was studied after stimulation of normal human adherent monocytes with F(ab)2 and Fab fragments of monoclonal antibodies specific to CR1 and CR3. CD11a, CD11b, CD18, and CD35 was studied by flow cytometry on neutrophils and monocytes. The molecular species of PAF from stimulated monocytes were identified by reverse-phase high-performance liquid chromatography coupled with mass spectrometry. Results Anti-CR1 and anti-CR3 monoclonal antibodies induced a dose-dependent C-16 but not C-18 PAF production. The latter occurred also with mono-valent Fab fragments of both anti-CRl and anti-CR3 monoclonal antibodies, that were not internalized as seen by immunofluorescence. Adherence of monocytes to Cuprophan membranes was markedly higher (P>0.01) in membranes pretreated with fresh than with heat-inactivated normal plasma. However, the high adherence to fresh plasma-treated membranes wascompletely abrogated by coincubating the cells with Web 2170, a specific PAF receptor antagonist. This was not due to downregulation of adhesion molecules expression on leukocytes. Conclusions These studies implicate a crucial role of PAF in blood interaction with haemodialysis membranes that fix complement activated products.

Original languageEnglish
Pages (from-to)1679-1688
Number of pages10
JournalNephrology Dialysis Transplantation
Volume10
Issue number9
DOIs
Publication statusPublished - 1995

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Lymphocyte Function-Associated Antigen-1
Platelet Activating Factor
Renal Dialysis
Monocytes
Membranes
Immunoglobulin Fab Fragments
Monoclonal Antibodies
Complement Receptors
Inflammation Mediators
Reverse-Phase Chromatography
Fluorescent Antibody Technique
Mass Spectrometry
Flow Cytometry
Neutrophils
Leukocytes
Down-Regulation
Hot Temperature
High Pressure Liquid Chromatography
Cell Membrane

Keywords

  • Biocompatibility
  • Monocyte
  • Paf

ASJC Scopus subject areas

  • Nephrology
  • Transplantation

Cite this

Adherence of human monocytes to haemodialysis membranes : LFA 1 (CDlla/CD18) CR1 (CD35) and CR3 (CDllb/CD18) triggering promotes the biosynthesis of platelet-activating factor and adherence. / Tetta, C.; Tropea, F.; Camussi, G.; Neri, R.; Wratten, L.; Sereni, L.; Silvestro, L.; Franceschi, C.; Haeffner-Cavaillon, N.

In: Nephrology Dialysis Transplantation, Vol. 10, No. 9, 1995, p. 1679-1688.

Research output: Contribution to journalArticle

Tetta, C. ; Tropea, F. ; Camussi, G. ; Neri, R. ; Wratten, L. ; Sereni, L. ; Silvestro, L. ; Franceschi, C. ; Haeffner-Cavaillon, N. / Adherence of human monocytes to haemodialysis membranes : LFA 1 (CDlla/CD18) CR1 (CD35) and CR3 (CDllb/CD18) triggering promotes the biosynthesis of platelet-activating factor and adherence. In: Nephrology Dialysis Transplantation. 1995 ; Vol. 10, No. 9. pp. 1679-1688.
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abstract = "Background Platelet-activating factor is a mediator of inflammation involved in the blood-membrane interaction.We report that selective stimulation of complement receptors (CR1 and CR3) triggers PAF synthesis and monocyte adherenceto complement-activating membranes. Methods The synthesis of PAF was studied after stimulation of normal human adherent monocytes with F(ab)2 and Fab fragments of monoclonal antibodies specific to CR1 and CR3. CD11a, CD11b, CD18, and CD35 was studied by flow cytometry on neutrophils and monocytes. The molecular species of PAF from stimulated monocytes were identified by reverse-phase high-performance liquid chromatography coupled with mass spectrometry. Results Anti-CR1 and anti-CR3 monoclonal antibodies induced a dose-dependent C-16 but not C-18 PAF production. The latter occurred also with mono-valent Fab fragments of both anti-CRl and anti-CR3 monoclonal antibodies, that were not internalized as seen by immunofluorescence. Adherence of monocytes to Cuprophan membranes was markedly higher (P>0.01) in membranes pretreated with fresh than with heat-inactivated normal plasma. However, the high adherence to fresh plasma-treated membranes wascompletely abrogated by coincubating the cells with Web 2170, a specific PAF receptor antagonist. This was not due to downregulation of adhesion molecules expression on leukocytes. Conclusions These studies implicate a crucial role of PAF in blood interaction with haemodialysis membranes that fix complement activated products.",
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AU - Tetta, C.

AU - Tropea, F.

AU - Camussi, G.

AU - Neri, R.

AU - Wratten, L.

AU - Sereni, L.

AU - Silvestro, L.

AU - Franceschi, C.

AU - Haeffner-Cavaillon, N.

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N2 - Background Platelet-activating factor is a mediator of inflammation involved in the blood-membrane interaction.We report that selective stimulation of complement receptors (CR1 and CR3) triggers PAF synthesis and monocyte adherenceto complement-activating membranes. Methods The synthesis of PAF was studied after stimulation of normal human adherent monocytes with F(ab)2 and Fab fragments of monoclonal antibodies specific to CR1 and CR3. CD11a, CD11b, CD18, and CD35 was studied by flow cytometry on neutrophils and monocytes. The molecular species of PAF from stimulated monocytes were identified by reverse-phase high-performance liquid chromatography coupled with mass spectrometry. Results Anti-CR1 and anti-CR3 monoclonal antibodies induced a dose-dependent C-16 but not C-18 PAF production. The latter occurred also with mono-valent Fab fragments of both anti-CRl and anti-CR3 monoclonal antibodies, that were not internalized as seen by immunofluorescence. Adherence of monocytes to Cuprophan membranes was markedly higher (P>0.01) in membranes pretreated with fresh than with heat-inactivated normal plasma. However, the high adherence to fresh plasma-treated membranes wascompletely abrogated by coincubating the cells with Web 2170, a specific PAF receptor antagonist. This was not due to downregulation of adhesion molecules expression on leukocytes. Conclusions These studies implicate a crucial role of PAF in blood interaction with haemodialysis membranes that fix complement activated products.

AB - Background Platelet-activating factor is a mediator of inflammation involved in the blood-membrane interaction.We report that selective stimulation of complement receptors (CR1 and CR3) triggers PAF synthesis and monocyte adherenceto complement-activating membranes. Methods The synthesis of PAF was studied after stimulation of normal human adherent monocytes with F(ab)2 and Fab fragments of monoclonal antibodies specific to CR1 and CR3. CD11a, CD11b, CD18, and CD35 was studied by flow cytometry on neutrophils and monocytes. The molecular species of PAF from stimulated monocytes were identified by reverse-phase high-performance liquid chromatography coupled with mass spectrometry. Results Anti-CR1 and anti-CR3 monoclonal antibodies induced a dose-dependent C-16 but not C-18 PAF production. The latter occurred also with mono-valent Fab fragments of both anti-CRl and anti-CR3 monoclonal antibodies, that were not internalized as seen by immunofluorescence. Adherence of monocytes to Cuprophan membranes was markedly higher (P>0.01) in membranes pretreated with fresh than with heat-inactivated normal plasma. However, the high adherence to fresh plasma-treated membranes wascompletely abrogated by coincubating the cells with Web 2170, a specific PAF receptor antagonist. This was not due to downregulation of adhesion molecules expression on leukocytes. Conclusions These studies implicate a crucial role of PAF in blood interaction with haemodialysis membranes that fix complement activated products.

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