Poste G, Papahadjopoulos D, Nicolson G L
Proc Natl Acad Sci U S A. 1975 Nov;72(11):4430-4. doi: 10.1073/pnas.72.11.4430.
Tertiary amine local anesthetics facilitated concanavalin A-induced redistribution of lectin receptors on murine BALB/3T3 cells and enhanced the susceptibility of these cells to agglutination by concanavalin A. In contrast, these drugs at similar concentrations inhibited ligand-induced capping of immunoglobulin receptors on mouse lymphocytes. We propose that these differing effects of local anesthetics on membrane receptor mobility in fibroblasts and lymphocytes result from the action of anesthetics on membrane-associated microtubules and microfilaments involved in the transmembrane control of receptor mobility. We present electron microscopic evidence of structural alterations in microtubule and microfilament organization in anesthetic-treated cells, together with data on changes in the responsiveness of anesthetic-treated cells to drugs that act on microtubules and/or microfilaments. This evidence supports the proposal that anesthetics affect the organization of cytoskeletal components or their plasma membrane attachment points. The effects of local anesthetics on ligand-induced redistribution of membrane receptors in both 3T3 cells and lymphocytes can be duplicated by treating cells with colchicine (or Vinca alkaloids) together with cytochalasin B. We propose that the participation of membrane-associated microtubules and microfilaments in the transmembrane control of receptor mobility is such that microtubules and microfilaments play opposing roles in regulating the mobility and topography of cell surface receptors.
叔胺类局部麻醉药可促进伴刀豆球蛋白A诱导的凝集素受体在小鼠BALB/3T3细胞上的重新分布,并增强这些细胞对伴刀豆球蛋白A凝集作用的敏感性。相反,这些药物在相似浓度下可抑制配体诱导的小鼠淋巴细胞免疫球蛋白受体的帽化。我们认为局部麻醉药对成纤维细胞和淋巴细胞膜受体流动性的这些不同作用,是由于麻醉药作用于参与受体流动性跨膜调控的膜相关微管和微丝所致。我们提供了经麻醉药处理的细胞中微管和微丝组织结构改变的电子显微镜证据,以及经麻醉药处理的细胞对作用于微管和/或微丝的药物反应性变化的数据。这些证据支持了麻醉药影响细胞骨架成分的组织或其质膜附着点的观点。局部麻醉药对3T3细胞和淋巴细胞中配体诱导的膜受体重新分布的作用,可用秋水仙碱(或长春花生物碱)与细胞松弛素B共同处理细胞来复制。我们认为,膜相关微管和微丝参与受体流动性的跨膜调控作用,使得微管和微丝在调节细胞表面受体的流动性和拓扑结构中发挥相反的作用。