Literature DB >> 9824771

Changes in neutrophil surface phenotype during hemodialysis.

K M Skubitz1, J Butterfield, K Ma, A P Skubitz.   

Abstract

The initiation of hemodialysis using cuprophane membranes is followed by a rapid fall in the circulating neutrophil count. This neutropenia is caused by a transient sequestration of neutrophils in the lung due to homotypic aggregation, largely in response to generation of C5a by contact of plasma with the dialyzer. The transient nature of hemodialysis neutropenia is due to desensitization of neutrophils to stimulation by C5a, thus demonstrating desensitization in vivo. To examine the in vivo effects on surface phenotype of continuous exposure of neutrophils to C5a over 3 h, the surface expression of 22 antigens was examined by flow cytometry in patients undergoing dialysis. Neutropenia was prominent at 15 min and absent at 60 and 180 min of dialysis. CD10, CD11b, CD11c, CD13, CD18, CD35, CD45, CD66acde, and CD66b were upregulated at 15 min and remained upregulated at 180 min. CD61 and CD63 increased slightly at 15 min and returned to baseline by 180 min. CD16 and CD62L were down regulated at 15 min and normalized by 180 min. CD15s, CDw17, CD32, and CD44 were slightly down regulated at 15 min and then returned to baseline by 180 min. CD11a, CD15, CD24, CD31, and CDw65 did not change during dialysis. This study demonstrates the changes in surface phenotype of neutrophils during prolonged in vivo exposure to C5a over 3 h, during which time neutrophils become desensitized to subsequent stimulation by similar concentrations of C5a but maintain responsiveness to other chemotactic stimuli.

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Year:  1998        PMID: 9824771     DOI: 10.1023/a:1022358313030

Source DB:  PubMed          Journal:  Inflammation        ISSN: 0360-3997            Impact factor:   4.092


  34 in total

1.  Modulation of granulocyte LAM-1 and MAC-1 during dialysis--a prospective, randomized controlled trial.

Authors:  J Himmelfarb; P Zaoui; R Hakim
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2.  Membrane surface antigen expression on neutrophils: a reappraisal of the use of surface markers for neutrophil activation.

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Journal:  Blood       Date:  1991-08-15       Impact factor: 22.113

3.  CD66a, CD66b, CD66c, and CD66d each independently stimulate neutrophils.

Authors:  K M Skubitz; K D Campbell; A P Skubitz
Journal:  J Leukoc Biol       Date:  1996-07       Impact factor: 4.962

4.  CD63 associates with tyrosine kinase activity and CD11/CD18, and transmits an activation signal in neutrophils.

Authors:  K M Skubitz; K D Campbell; J Iida; A P Skubitz
Journal:  J Immunol       Date:  1996-10-15       Impact factor: 5.422

5.  Up-regulation of the iC3b receptor (CR3) is neither necessary nor sufficient to promote neutrophil aggregation.

Authors:  M R Philips; J P Buyon; R Winchester; G Weissmann; S B Abramson
Journal:  J Clin Invest       Date:  1988-08       Impact factor: 14.808

6.  CDw17: a neutrophil glycolipid antigen regulated by activation.

Authors:  F W Symington
Journal:  J Immunol       Date:  1989-04-15       Impact factor: 5.422

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Journal:  Clin Nephrol       Date:  1993-03       Impact factor: 0.975

8.  Differentially regulated cell surface expression of leukocyte adhesion receptors on neutrophils.

Authors:  V Alvarez; R Pulido; M R Campanero; V Paraiso; M O de Landázuri; F Sánchez-Madrid
Journal:  Kidney Int       Date:  1991-11       Impact factor: 10.612

9.  Biochemical and functional characterization of the leucocyte tyrosine phosphatase CD45 (CD45RO, 180 kD) from human neutrophils. In vivo upregulation of CD45RO plasma membrane expression on patients undergoing haemodialysis.

Authors:  R Pulido; V Alvarez; F Mollinedo; F Sánchez-Madrid
Journal:  Clin Exp Immunol       Date:  1992-02       Impact factor: 4.330

10.  Mobilization of an intracellular glycoprotein (Mac-1) on monocytes and granulocytes during hemodialysis.

Authors:  P Thylén; J Lundahl; E Fernvik; J Hed; S B Svenson; S H Jacobson
Journal:  Am J Nephrol       Date:  1992       Impact factor: 3.754

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  1 in total

1.  A novel method for isolation of neutrophils from murine blood using negative immunomagnetic separation.

Authors:  M J Cotter; K E Norman; P G Hellewell; V C Ridger
Journal:  Am J Pathol       Date:  2001-08       Impact factor: 4.307

  1 in total

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