Li, Hz., Lu, Yh., Huang, Gs. et al. Tanshinone II A inhibits dendritic cell-mediated adaptive immunity: Potential role in anti-atherosclerotic activity., Chin. J. Integr. Med. 20, 764–769 (2014). https://doi.org/10.1007/s11655-012-1213-9
Hong-zhan Li, Yong-heng Lu, Guang-sheng Huang, et al. Tanshinone II A inhibits dendritic cell-mediated adaptive immunity: Potential role in anti-atherosclerotic activity[J]. Chinese Journal of Integrative Medicine, 2014,20(10):764-769.
Li, Hz., Lu, Yh., Huang, Gs. et al. Tanshinone II A inhibits dendritic cell-mediated adaptive immunity: Potential role in anti-atherosclerotic activity., Chin. J. Integr. Med. 20, 764–769 (2014). https://doi.org/10.1007/s11655-012-1213-9DOI:
Hong-zhan Li, Yong-heng Lu, Guang-sheng Huang, et al. Tanshinone II A inhibits dendritic cell-mediated adaptive immunity: Potential role in anti-atherosclerotic activity[J]. Chinese Journal of Integrative Medicine, 2014,20(10):764-769. DOI: 10.1007/s11655-012-1213-9.
Tanshinone II A inhibits dendritic cell-mediated adaptive immunity: Potential role in anti-atherosclerotic activity
摘要
Antigen-presenting cells such as monocytes and dendritic cells (DCs) stimulate T-cell proliferation and activation during adaptive immunity. This cellular interaction plays a role in the growth of atherosclerotic plaques. Tanshinone II A (TSN) had been shown to decrease the growth of atherosclerotic lesions. We therefore investigated the ability of TSN to inhibit human monocyte-derived DCs and their T-cellstimulatory capacity. DCs derived from human monocytes cultured with recombinant human interleukin (IL)-4 and recombinant human granulocyte-macrophage colony-stimulating factor were co-cultured with TSN and lipopolysaccharide for 48 h. Phosphate-buffered saline was used as a negative control. Activation markers and the capacity of DCs for endocytosis were measured by flow cytometry
and proinflammatory cytokines were measured by enzyme-linked immunosorbent assays. DCs were co-cultured with lymphocytes to measure T-cell proliferation and IL-2 secretion by mixed lymphocyte reactions. TSN dose-dependently attenuated DC expression of costimulatory molecules (CD86)
and decreased expression of major histocompatibility complex class II (human loukocyte antigen-DR) and adhesion molecules (CD54). Moreover
TSN reduced secretion of the proinflammatory cytokines IL-12 and IL-1 by human DCs
and restored the capacity for endocytosis. Finally
TSN-preincubated DCs showed a reduced capacity to stimulate T-cell proliferation and cytokine secretion. TSN inhibits DC maturation and decreases the expression of proinflammatory cytokines
while impairing their capacity to stimulate T-cell proliferation and cytokine secretion. These effects may contribute to the influence of TSN on the progression of atherosclerotic lesions.
Abstract
Antigen-presenting cells such as monocytes and dendritic cells (DCs) stimulate T-cell proliferation and activation during adaptive immunity. This cellular interaction plays a role in the growth of atherosclerotic plaques. Tanshinone II A (TSN) had been shown to decrease the growth of atherosclerotic lesions. We therefore investigated the ability of TSN to inhibit human monocyte-derived DCs and their T-cellstimulatory capacity. DCs derived from human monocytes cultured with recombinant human interleukin (IL)-4 and recombinant human granulocyte-macrophage colony-stimulating factor were co-cultured with TSN and lipopolysaccharide for 48 h. Phosphate-buffered saline was used as a negative control. Activation markers and the capacity of DCs for endocytosis were measured by flow cytometry
and proinflammatory cytokines were measured by enzyme-linked immunosorbent assays. DCs were co-cultured with lymphocytes to measure T-cell proliferation and IL-2 secretion by mixed lymphocyte reactions. TSN dose-dependently attenuated DC expression of costimulatory molecules (CD86)
and decreased expression of major histocompatibility complex class II (human loukocyte antigen-DR) and adhesion molecules (CD54). Moreover
TSN reduced secretion of the proinflammatory cytokines IL-12 and IL-1 by human DCs
and restored the capacity for endocytosis. Finally
TSN-preincubated DCs showed a reduced capacity to stimulate T-cell proliferation and cytokine secretion. TSN inhibits DC maturation and decreases the expression of proinflammatory cytokines
while impairing their capacity to stimulate T-cell proliferation and cytokine secretion. These effects may contribute to the influence of TSN on the progression of atherosclerotic lesions.
关键词
dendritic cellsimmunityatherosclerosistanshinone II A
Keywords
dendritic cellsimmunityatherosclerosistanshinone II A
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相关作者
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相关机构
Institute of Basic Theories of Traditional Chinese Medicine, China Academy of Traditional Chinese Medicine
Department of Oncology, Clifford Hospital of Guangzhou University of Traditional Chinese Medicine
Department of Gynaecology and Obstetrics, Shenzhen Baoan Maternal and Child Health Hospital
Department of Obstetrics and Gynecology, First Affiliated Hospital of Jinan University
Shandong Provincial Corps Hospital of Chinese People’s Armed Police Forces