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药用植物柴胡根中果胶多糖的B细胞增殖活性及其结构要求

B-cell proliferation activity of pectic polysaccharide from a medicinal herb, the roots of Bupleurum falcatum L. and its structural requirement.

作者信息

Sakurai M H, Matsumoto T, Kiyohara H, Yamada H

机构信息

Oriental Medicine Research Center, The Kitasato Institute, Tokyo, Japan.

出版信息

Immunology. 1999 Jul;97(3):540-7. doi: 10.1046/j.1365-2567.1999.00774.x.

Abstract

Pectic polysaccharide fraction (BR-2) containing pharmacologically active pectic polysaccharide, bupleuran 2IIc, which was prepared from a medicinal herb, the roots of Bupleurum falcatum L., was administered orally to C3H/HeJ mice for 7 consecutive days. Proliferative responses of spleen cells were enhanced in the presence of the purified pectic polysaccharide, bupleuran 2IIc, but another B-cell mitogen, lipopolysaccharide (LPS) did not give a similar effect. In vitro studies using spleen cells showed that bupleuran 2IIc also stimulated lymphocytes, depleted of adherent cells or T cells. Bupleuran 2IIc treatment increased subpopulation of CD25+ and surface immunoglobulin M-positive (sIgM+) lymphocytes. Non-specific immunoglobulin secretion of spleen cells treated with bupleuran 2IIc was increased according to the culture time, and coexistence of interleukin-6 (IL-6) enhanced the secretion more than that of bupleuran 2IIc alone. These results suggest that bupleuran 2IIc proliferates B cells in the absence of macrophages, and the resulting activated B cells are then induced into antibody-forming cells in the presence of IL-6. Among the structural region of bupleuran 2IIc, ramified region (PG-1), which consists of rhamnogalacturonan core rich in neutral sugar chain, showed the potent mitogenic activity suggesting it to be an active site. Mitogenic activity of bupleuran 2IIc was reduced in the presence of antipolysaccharide antibody (antibupleuran 2IIc/PG-1-IgG), which recognizes the ramified region of bupleuran 2IIc as the antigenic epitope. Mitogenic activity of bupleuran 2IIc was also reduced by the addition of beta-d-GlcpA-(1-->6)-beta-d-Galp-(1-->6)-d-Galp or beta-d-GlcpA-(1-->6)-d-Galp, which are a part of the epitopes of antibupleuran 2IIc/PG-1-IgG. These results suggest that the epitopes in bupleuran 2IIc act as active sites of the polysaccharide during mitogenic activity.

摘要

从药用植物柴胡(Bupleurum falcatum L.)的根中制备得到含有具有药理活性的果胶多糖柴胡皂苷2IIc的果胶多糖级分(BR-2),将其连续7天口服给予C3H/HeJ小鼠。在纯化的果胶多糖柴胡皂苷2IIc存在的情况下,脾细胞的增殖反应增强,但另一种B细胞有丝分裂原脂多糖(LPS)没有产生类似的效果。使用脾细胞进行的体外研究表明,柴胡皂苷2IIc也能刺激去除贴壁细胞或T细胞后的淋巴细胞。柴胡皂苷2IIc处理增加了CD25 +和表面免疫球蛋白M阳性(sIgM +)淋巴细胞的亚群。用柴胡皂苷2IIc处理的脾细胞的非特异性免疫球蛋白分泌随培养时间增加,并且白细胞介素-6(IL-6)的共存比单独使用柴胡皂苷2IIc更能增强分泌。这些结果表明,柴胡皂苷2IIc在没有巨噬细胞的情况下使B细胞增殖,并且在IL-6存在的情况下,由此产生的活化B细胞随后被诱导成为抗体形成细胞。在柴胡皂苷2IIc的结构区域中,由富含中性糖链的鼠李半乳糖醛酸聚糖核心组成的分支区域(PG-1)显示出强大的促有丝分裂活性,表明它是一个活性位点。在识别柴胡皂苷2IIc的分支区域作为抗原表位的抗多糖抗体(抗柴胡皂苷2IIc / PG-1-IgG)存在的情况下,柴胡皂苷2IIc的促有丝分裂活性降低。添加β-d-GlcpA-(1→6)-β-d-Galp-(1→6)-d-Galp或β-d-GlcpA-(1→6)-d-Galp(它们是抗柴胡皂苷2IIc / PG-1-IgG表位的一部分)也会降低柴胡皂苷2IIc的促有丝分裂活性。这些结果表明,柴胡皂苷2IIc中的表位在促有丝分裂活性期间作为多糖的活性位点。

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