Literature DB >> 8419075

Modulation of CD4 by suramin.

P D Allen1, D H Johnston, M G Macey, N S Williams, A C Newland.   

Abstract

Suramin is a polysulphonated compound which can selectively bind to, and inhibit the activity of, a wide range of growth factors. There has been renewed interest recently in suramin as an anti-cancer agent and therefore we have studied its effects on lymphocyte subset populations and recombinant human IL-2 (rhIL-2) activation on lymphocytes in vitro. In the presence of rhIL-2 (1000 U/ml), suramin (200 micrograms/ml) caused a decrease in percentage of cells expressing the predominantly T cell antigen CD3; no change in percentage of cells expressing the T suppressor/cytotoxic subset antigen, CD8; a small rise in those expressing the natural killer cell antigen, CD56; and a large significant fall in those expressing the T helper subset antigen CD4 (48.51% versus 27.97%; P < 0.001). CD4 modulation by suramin was also found on the CD4+ cell lines CEM and MOLT-4. The effect of suramin on rhIL-2-induced activation antigen expression remains equivocal, since a small rise in CD25 expression and small falls in CD71 and HLA-Dr expression were recorded. The modulatory effect of suramin on CD4 expression was not reversible over a 96-h culture period in its continued presence. However, on removal of suramin by extensive washing, recovery of CD4 expression was detected within 24 h. Suramin-induced modulation, but not PMA-induced modulation, could be partially inhibited by preincubation with tyrphostin (12 microM), a tyrosine kinase inhibitor.

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Year:  1993        PMID: 8419075      PMCID: PMC1554663          DOI: 10.1111/j.1365-2249.1993.tb03369.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN: 0009-9104            Impact factor:   4.330


  34 in total

1.  Circulating glycosaminoglycan anticoagulants associated with suramin treatment.

Authors:  M K Horne; C A Stein; R V LaRocca; C E Myers
Journal:  Blood       Date:  1988-02       Impact factor: 22.113

Review 2.  CD4+ T cells: specificity and function.

Authors:  C A Janeway; S Carding; B Jones; J Murray; P Portoles; R Rasmussen; J Rojo; K Saizawa; J West; K Bottomly
Journal:  Immunol Rev       Date:  1988-01       Impact factor: 12.988

3.  Phosphorylation of CD4 and CD8 molecules following T cell triggering.

Authors:  M L Blue; D A Hafler; K A Craig; H Levine; S F Schlossman
Journal:  J Immunol       Date:  1987-12-15       Impact factor: 5.422

4.  Cell-cell adhesion mediated by CD8 and MHC class I molecules.

Authors:  A M Norment; R D Salter; P Parham; V H Engelhard; D R Littman
Journal:  Nature       Date:  1988-11-03       Impact factor: 49.962

5.  Suramin: a potent inhibitor of the reverse transcriptase of RNA tumor viruses.

Authors:  E De Clercq
Journal:  Cancer Lett       Date:  1979-11       Impact factor: 8.679

6.  The CD4 and CD8 antigens are coupled to a protein-tyrosine kinase (p56lck) that phosphorylates the CD3 complex.

Authors:  E K Barber; J D Dasgupta; S F Schlossman; J M Trevillyan; C E Rudd
Journal:  Proc Natl Acad Sci U S A       Date:  1989-05       Impact factor: 11.205

7.  Specific interaction of aurintricarboxylic acid with the human immunodeficiency virus/CD4 cell receptor.

Authors:  D Schols; M Baba; R Pauwels; J Desmyter; E De Clercq
Journal:  Proc Natl Acad Sci U S A       Date:  1989-05       Impact factor: 11.205

8.  Effects of suramin on complement, blood clotting, fibrinolysis and kinin formation.

Authors:  V Eisen; C Loveday
Journal:  Br J Pharmacol       Date:  1973-12       Impact factor: 8.739

9.  The CD4 receptor is complexed in detergent lysates to a protein-tyrosine kinase (pp58) from human T lymphocytes.

Authors:  C E Rudd; J M Trevillyan; J D Dasgupta; L L Wong; S F Schlossman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-07       Impact factor: 11.205

10.  Suramin inhibits cell growth and glycolytic activity and triggers differentiation of human colic adenocarcinoma cell clone HT29-D4.

Authors:  J Fantini; J B Rognoni; M Roccabianca; G Pommier; J Marvaldi
Journal:  J Biol Chem       Date:  1989-06-15       Impact factor: 5.157

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