Stanton P K, Sarvey J M, Moskal J R
Proc Natl Acad Sci U S A. 1987 Mar;84(6):1684-8. doi: 10.1073/pnas.84.6.1684.
Monoclonal antibodies generated to 5-day-old postnatal rat dentate gyri were tested for their effects on long-term potentiation (LTP) in rat hippocampal slices. One antibody, B6E11, was found to block the production of LTP and to suppress established LTP in both area CA1 of the hippocampus and the dentate gyrus. In CA1, B6E11 was effective only when applied to the apical dendrites synapsing with the potentiating input. The production of LTP could not be blocked if B6E11 was applied to the cell bodies or to the basal dendrites of CA1. In field CA1, B6E11 had no effect on the production of short-term potentiation. Another monoclonal antibody from the same panel as B6E11, of the same immunoglobulin class, which also binds to hippocampal neurons similarly to B6E11, had no effect on LTP production. These results supply evidence that B6E11 modulates LTP by an interaction with a specific cell-surface protein associated with the dendrites of neurons in both dentate gyrus and CA1 regions.
对出生后5天的大鼠齿状回产生的单克隆抗体进行了测试,以观察它们对大鼠海马切片中长时程增强(LTP)的影响。发现一种抗体B6E11可阻断LTP的产生,并抑制海马体CA1区和齿状回中已建立的LTP。在CA1区,B6E11仅在应用于与增强输入突触连接的顶端树突时才有效。如果将B6E11应用于CA1区的细胞体或基底树突,则无法阻断LTP的产生。在CA1区,B6E11对短期增强的产生没有影响。与B6E11来自同一组、免疫球蛋白类别相同、与海马神经元结合方式也与B6E11相似的另一种单克隆抗体,对LTP的产生没有影响。这些结果提供了证据,表明B6E11通过与齿状回和CA1区神经元树突相关的特定细胞表面蛋白相互作用来调节LTP。