Muchmore A V, Decker J M, Blaese R M
J Immunol. 1980 Sep;125(3):1306-11.
We have previously shown that monosaccharides and disaccharides will block the expression of spontneous monocyte-mediated cytotoxicity. Our data were consistent with the hypothesis that human mononuclear cells express lectin-like receptors that are capable of binding to a variety sugar moieties found on target cell membranes. In this communication, we will present evidence that monosaccharides and disaccharides are also capable of blocking the expression of T cell reactivity as measured by an in vitro antigen-specific proliferative assay. The majority of sugars that blocked monocyte-mediated cytotoxicity had no effect on antigen-specific proliferation. Those sugars that did suppress antigen-induced proliferation had no effect on PHA-induced proliferation. Furthermore, some of these sugars only inhibited if they were added at the initiation of the assay; they failed to inhibit if added 24 hr after the initiation of the assay. Antigen-pulsing experiments suggested that these sugars did not block antigen uptake by human monocytes. These data suggest that a variety of cellular interactions may be mediated by receptors with specificity for simple sugars. The ability to block these naturally occurring lectins specifically both in vitro and in vivo may prove to be a powerful tool for dissecting out various forms of cellular recognition and collaboration.
我们之前已经表明,单糖和双糖会阻断自发单核细胞介导的细胞毒性的表达。我们的数据与以下假设一致:人类单核细胞表达凝集素样受体,这些受体能够结合靶细胞膜上发现的多种糖部分。在本通讯中,我们将提供证据表明,通过体外抗原特异性增殖试验测定,单糖和双糖也能够阻断T细胞反应性的表达。大多数阻断单核细胞介导的细胞毒性的糖对抗原特异性增殖没有影响。那些确实抑制抗原诱导增殖的糖对PHA诱导的增殖没有影响。此外,其中一些糖只有在试验开始时添加才会抑制;如果在试验开始24小时后添加则不会抑制。抗原脉冲实验表明,这些糖不会阻断人类单核细胞对抗原的摄取。这些数据表明,多种细胞相互作用可能由对单糖具有特异性的受体介导。在体外和体内特异性阻断这些天然存在的凝集素的能力可能被证明是剖析各种形式的细胞识别和协作的有力工具。