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化学交联的(1→3)-β-D-葡聚糖在体外激活巨噬细胞

Macrophage activation in vitro by chemically cross-linked (1----3)-beta-D-glucans.

作者信息

Adachi Y, Ohno N, Ohsawa M, Oikawa S, Yadomae T

机构信息

Tokyo College of Pharmacy, Japan.

出版信息

Chem Pharm Bull (Tokyo). 1990 Apr;38(4):988-92. doi: 10.1248/cpb.38.988.

Abstract

The chemical cross-linking of soluble (1----3)-beta-D-glucans having molecular weights of 21000 (CL 3 h) and 6400 (CL 6 h), and laminarin (CL LAMI), which showed negligible biological activity, by epichlorohydrin provided rigid particles. These particles showed no gel-to-sol transition upon the addition of sodium hydroxide. We compared the effects of chemical cross-linking on the biological activities of glucans. The alternative complement pathway was not activated by any of the cross-linked glucans. Glucose consumption, lysosomal enzyme release, and interleukin-1 production by mouse resident peritoneal macrophages incubated in vitro were strongly induced by CL 3 h, CL 6 h and CL LAMI. However, cross-linked dextran, Sephadex, did not exhibit any of these biological activities. These results suggested that chemical cross-linking of (1----3)-beta-D-glucans enhances macrophage activities without opsonization by complement components.

摘要

通过环氧氯丙烷对分子量分别为21000(CL 3小时)和6400(CL 6小时)的可溶性(1→3)-β-D-葡聚糖以及生物活性可忽略不计的海带多糖(CL LAMI)进行化学交联,得到了刚性颗粒。这些颗粒在加入氢氧化钠后未表现出凝胶-溶胶转变。我们比较了化学交联对葡聚糖生物活性的影响。任何一种交联葡聚糖均未激活替代补体途径。体外培养的小鼠腹腔常驻巨噬细胞的葡萄糖消耗、溶酶体酶释放及白细胞介素-1产生受到CL 3小时、CL 6小时和CL LAMI的强烈诱导。然而,交联葡聚糖Sephadex未表现出任何这些生物活性。这些结果表明,(1→3)-β-D-葡聚糖的化学交联增强了巨噬细胞活性,而无需补体成分的调理作用。

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