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首页> 外文期刊>International immunopharmacology >Toll-like receptor-mediated activation of B cells and macrophages by polysaccharide isolated from cell culture of Acanthopanax senticosus.
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Toll-like receptor-mediated activation of B cells and macrophages by polysaccharide isolated from cell culture of Acanthopanax senticosus.

机译:从刺五加的细胞培养物中分离出的多糖由Toll样受体介导的B细胞和巨噬细胞的激活。

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摘要

We investigated the mechanism of the immunomodulatory action of polysaccharide (ASP) isolated from a cell culture of Acanthopanax senticosus. ASP was found to directly increase the proliferation and differentiation of B cells, and the cytokine production of macrophage, but not the proliferation and cytokine production of T cells. Since ASP cannot penetrate the cell membrane due to its large molecular mass, such cellular activation may be caused by the surface binding of ASP to receptors expressed on B cells and macrophages. The possibility that TLRs, which are known to be involved in immune-related responses, may be the receptor(s) of ASP was investigated. The immunomodulating activities of ASP on the B cells and macrophages of C3H/HeJ mice, expressing a defective toll-like receptor (TLR)-4, were decreased versus the corresponding cells from C3H/HeN mice. In addition, the activities of ASP on B cells and macrophages were significantly reduced by treating the cells with antibodies to TLR4 and TLR2 priorto ASP, suggesting that both of them are the possible receptors of ASP. The ligation of TLRs induced by ASP was able to activate mitogen-activated protein kinases (MAPKs), such as Erk1/2, p38 and JNK, and the transcription factor NF-kappaB. Although ASP was shown to activate the TLR signaling cascades in the same manner as lipopolysaccharide (LPS), these two could be differentiated by the finding that polymyxin B (PMB), a specific inhibitor of LPS, did not significantly affect the activities of ASP on B cells and macrophages. Taken together, our results demonstrate that ASP, isolated from a cell culture of A. senticosus, activates B cells and macrophages by interacting with TLRs and leading to the subsequent activation of mitogen-activated protein kinases and NF-kappaB.
机译:我们调查了从刺五加的细胞培养物中分离的多糖(ASP)的免疫调节作用的机制。发现ASP直接增加B细胞的增殖和分化以及巨噬细胞的细胞因子产生,但不增加T细胞的增殖和细胞因子产生。由于ASP由于分子量大而无法穿透细胞膜,因此这种细胞活化可能是由于ASP与B细胞和巨噬细胞上表达的受体的表面结合引起的。研究了已知与免疫相关反应有关的TLR可能是ASP受体的可能性。与来自C3H / HeN小鼠的相应细胞相比,ASP对表达缺陷型toll样受体(TLR)-4的B细胞和C3H / HeJ小鼠巨噬细胞的免疫调节活性降低。此外,在ASP之前用TLR4和TLR2抗体处理细胞后,ASP对B细胞和巨噬细胞的活性大大降低,这表明它们都是ASP的可能受体。由ASP诱导的TLR的连接能够激活有丝分裂原激活的蛋白激酶(MAPK),例如Erk1 / 2,p38和JNK,以及转录因子NF-kappaB。尽管显示ASP以与脂多糖(LPS)相同的方式激活TLR信号级联,但可以通过发现LPS的特异性抑制剂多粘菌素B(PMB)不会显着影响ASP对TPS的活性来区分这两者。 B细胞和巨噬细胞。两者合计,我们的结果表明,从A. senticosus的细胞培养物中分离得到的ASP通过与TLR相互作用激活B细胞和巨噬细胞,并导致随后的丝裂原激活的蛋白激酶和NF-κB的激活。

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