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大分子的肠道摄取。V. 抗体或抗原过量制备的抗原 - 抗体复合物在大鼠小肠中的体外摄取比较。

Intestinal uptake of macromolecules. V. Comparison of the in vitro uptake by rat small intestine of antigen-antibody complexes prepared in antibody or antigen excess.

作者信息

Walker W A, Abel S N, Wu M, Bloch K J

出版信息

J Immunol. 1976 Sep;117(3):1028-32.

PMID:956647
Abstract

The in vitro absorption by rat jejunal and ileal gut sacs of soluble antigen-antibody complexes and of antigen alone was compared. Complexes prepared in 2-fold antibody excess were absorbed in significantly smaller quantities than was antigen alone. Complexes prepared in 50-fold antigen excess were absorbed by jejunal gut sacs in quantities equivalent to that antigen alone, whereas the absorption of such complexes by ileal sacs was somewhat decreased compared to that of antigen. There was less radiolabeled antigen tightly bound to the intestinal mucosa of gut sacs exposed to complexes prepared in antigen or antibody excess compared to antigen alone. Complexes prepared in antibody excess appeared to stimulate secretion of mucus and complexes were associated with the mucus fraction. It was suggested that the large size of complexes prepared in antibody excess may result in their trapping in the mucus coat of the gut, thereby preventing contact with the surface of the enterocyte from whence uptake by pinocytosis is initiated. In addition, complexes appear to be shed from the surface with mucus by a mechanism still to be elucidated.

摘要

比较了大鼠空肠和回肠肠囊对可溶性抗原-抗体复合物及单独抗原的体外吸收情况。在抗体过量两倍的情况下制备的复合物吸收量明显少于单独的抗原。在抗原过量50倍的情况下制备的复合物,空肠肠囊对其吸收量与单独抗原相当,而回肠肠囊对这类复合物的吸收与抗原相比略有减少。与单独抗原相比,暴露于抗原或抗体过量情况下制备的复合物的肠囊肠黏膜紧密结合的放射性标记抗原较少。抗体过量情况下制备的复合物似乎刺激了黏液分泌,且复合物与黏液部分相关。有人提出,抗体过量情况下制备的复合物体积较大,可能会被困在肠道的黏液层中,从而阻止与肠细胞表面接触,而从肠细胞表面开始通过胞饮作用进行摄取。此外,复合物似乎通过一种尚待阐明的机制与黏液一起从表面脱落。

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