2000
DOI: 10.1159/000026424
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Time-Dependent Effect of Cyclosporine on Mitogenic Responses and Lymphocyte Subset Populations in Rat Spleen and Submaxillary Lymph Nodes

Abstract: Lipopolysaccharide (LPS)- and concanavalin A (ConA)-induced proliferation and T lymphocyte subsets were measured in spleen and submaxillary lymph nodes of male rats injected with cyclosporine (5 mg/kg s.c. for 5 days, at 12.00 or 24.00 h; animals kept under light from 08.00 to 20.00 h daily). One hour before the third injection, Freund’s complete adjuvant or its vehicle was administered. A suppressive effect of cyclosporine on the mitogenic action of LPS was seen in the spleen of rats injected with cyclosporin… Show more

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Cited by 7 publications
(3 citation statements)
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“…The relative size distributions of lymph cells in submaxillary lymph nodes of rats were determined by fluorescence‐activated cell sorter analysis, as previously described ( 13, 14). For these studies, we used the following monoclonal antibodies: Anti‐rat LCA (OX‐33) for B lymphocytes (Serotec, Oxford, UK), anti‐rat TCR alpha/beta (R7.3) for T lymphocytes (Serotec, Oxford, UK), anti‐rat CD4 (OX‐35) which recognizes a rat T helper cell differentiation antigen (Pharmingen, San Diego, CA, USA), and anti‐rat CD8a (OX‐8) which recognize the reactive antigen expressed on rat T cytotoxic/suppressor cells (Pharmingen).…”
Section: Methodsmentioning
confidence: 99%
“…The relative size distributions of lymph cells in submaxillary lymph nodes of rats were determined by fluorescence‐activated cell sorter analysis, as previously described ( 13, 14). For these studies, we used the following monoclonal antibodies: Anti‐rat LCA (OX‐33) for B lymphocytes (Serotec, Oxford, UK), anti‐rat TCR alpha/beta (R7.3) for T lymphocytes (Serotec, Oxford, UK), anti‐rat CD4 (OX‐35) which recognizes a rat T helper cell differentiation antigen (Pharmingen, San Diego, CA, USA), and anti‐rat CD8a (OX‐8) which recognize the reactive antigen expressed on rat T cytotoxic/suppressor cells (Pharmingen).…”
Section: Methodsmentioning
confidence: 99%
“…The subsets (T lymphocyte, B lymphocyte and NK cell) of lymphocytes were determined by a direct immunofluorescent staining with a flow cytometric analysis ( 35 ). We used the Rat T/B/NK Cell Cocktail (Fluorescence-labeled antibody cocktail, Becton Dickinson, USA): APC-conjugated CD3 for T lymphocyte (clone 1F4); fluoresce in isothiocyanate (FITC)-conjugated anti-rat CD45RA for B lymphocyte (clone OX-33); and Phycoerythrin (PE)-conjugated anti-rat CD161a for NK cells (clone 10/78).…”
Section: Methodsmentioning
confidence: 99%
“…Splenocyte proliferation was evaluated after in vitro stimulation with Concanavalin A (ConA5μg/mL), Phytohaemagglutinin A (PHA) and Lypopolysaccharide (LPS 3 μg/mL). These three mitogens are commonly reported to display cell proliferation [31][32][33][34]. The CFSE fluorescence intensity is inversely correlated with cell proliferation.…”
Section: Cell Proliferation Evaluationmentioning
confidence: 98%