Cremaschi G A, Sterin-Borda L
Centro de Estudios Farmacológicos y Botánicos (CEFYBO), CONICET, Buenos Aires, Argentina.
Acta Physiol Pharmacol Ther Latinoam. 1994;44(3):55-64.
Besides the important role of the Major Histocompatibility Complex (MHC) class I molecules n physiologically restricting immune responses, they seem to play a non-immunological function by the molecular association with several hormone receptors (R). Among the hormone R and class I antigen (Ag) interactions, insulin R, epidermal growth factor (EGF) R, interleukin-2 (IL-2) R, luteinizing (LH) hormone R, beta adrenergic R and muscarinic cholinergic R were described in several human and animal models. Evidences from immunoprecipitation assays, binding assays and immunofluorescence techniques pointed to the molecular association of all of these R with class I molecules on cellular surfaces. Only for beta adrenergic R, muscarinic cholinergic R and LH-R, antibodies directed against class I products were described to exert the activation of these R leading to the production of intracellular second messengers and consequently modifying the physiology of the corresponding cell. This was also obtained on insulin R with peptides derived from class I molecules. The selectivity or R involved in all studied cellular types, should find its explanation in the physiological importance of the considered R for the indicated cell. The participation of cytoskeletal proteins on these interactions and the proximity on cell surfaces between both molecules, probably managed by ligand-mediated microaggregation, are also facts to be taken into account to better understand the biological consequences of these interactions.
主要组织相容性复合体(MHC)I类分子在生理上限制免疫反应方面具有重要作用,此外,它们似乎还通过与几种激素受体(R)的分子结合发挥非免疫功能。在几种人类和动物模型中描述了激素R与I类抗原(Ag)之间的相互作用,包括胰岛素R、表皮生长因子(EGF)R、白细胞介素-2(IL-2)R、促黄体生成素(LH)激素R、β肾上腺素能R和毒蕈碱型胆碱能R。免疫沉淀试验、结合试验和免疫荧光技术的证据表明,所有这些R与细胞表面的I类分子存在分子结合。仅对于β肾上腺素能R、毒蕈碱型胆碱能R和LH-R,针对I类产物的抗体被描述为可激活这些R,导致细胞内第二信使的产生,从而改变相应细胞的生理功能。在胰岛素R上使用源自I类分子的肽也得到了同样的结果。所有研究细胞类型中涉及的R的选择性,应从所考虑的R对指定细胞的生理重要性中找到解释。细胞骨架蛋白在这些相互作用中的参与以及两种分子在细胞表面的接近程度(可能由配体介导的微聚集控制),也是为了更好地理解这些相互作用的生物学后果而需要考虑的因素。