Ouabain Decreases Regulatory T Cell Number in Mice by Reducing IL-2 Secretion

被引:6
|
作者
Carvalho da Silva, Joyle Moreira [1 ,2 ]
Azevedo, Augusto das Neves [1 ]
dos Santos Barbosa, Rebeca Pinheiro [1 ]
Teixeira, Mariana Pires [1 ,2 ]
Goncalves Vianna, Thais Andressa [1 ]
Fittipaldi, Juliana [1 ]
Cabral, Vinicius Ribeiro [3 ]
de Paiva, Luciana Souza [1 ,2 ]
机构
[1] Univ Fed Fluminense, Inst Biol, Dept Imunobiol, Niteroi, RJ, Brazil
[2] Univ Fed Fluminense, Programa Posgrad Patol, Niteroi, RJ, Brazil
[3] Univ Fed Fluminense, Fac Educ, Dept Fundamentos Pedag, Niteroi, RJ, Brazil
关键词
T lymphocytes; Spleen; Immune regulation; B-CELLS; TGF-BETA; FOXP3; EXPRESSION; ACTIVATION; INDUCTION; COMPOUND; DIFFERENTIATION; AUTOIMMUNITY; LYMPHOCYTES;
D O I
10.1159/000501720
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Ouabain (OUA) is a cardiotonic glycoside originally extracted from African plants. It has also been described as an endogenous component in mammals, being released in stress situations mainly by the adrenal gland. OUA has been reported to be capable of inhibiting mitogen-induced lymphocyte proliferation and also affects B and T lymphocytes. Objectives: The aim of this work is to show the effects of OUA in peripheral T lymphocytes. Methods: In the in vivo experiments, mice were injected intraperitoneally for 3 consecutive days with RPMI medium (control group) or 0.56 mg/kg of OUA diluted in RPMI medium (OUA group). On the fourth day, spleen or mesenteric lymph nodes were removed. Results: OUA significantly reduced the number of CD4+ T lymphocytes in the spleen, especially regulatory T cells (Tregs). In vitro OUA did not inhibit the proliferation of CD4(+)T lymphocytes stimulated with anti-CD3 neither was able to induce the apoptosis of CD4(+) nor Tregs. There was no increase in the number or percentage of T lymphocytes in the mesenteric lymph nodes, suggesting that there was no preferential accumulation of these cells in this organ. Secretion of IL-2 by activated T lymphocytes was decreased by the OUA, explaining at least in part the reduction of Tregs, since this cytokine is involved in the peripheral conversion and maintenance of Tregs. Conclusion: The impact of this reduction in autoimmune diseases, allergy and cancer as well as the potential use of OUA as a therapeutic approach in tumor treatment still needs more investigation.
引用
收藏
页码:188 / 197
页数:10
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