St-Pierre J A, Nouel D, Dumont Y, Beaudet A, Quirion R
Douglas Hospital Research Center, Verdun, Québec, Canada.
Glia. 2000 Mar;30(1):82-91.
The expression and pharmacological characterization of neuropeptide Y (NPY) receptors of the Y(1) subtype on cultured hippocampal neurons was reported using radioreceptor assays and immunohistochemical approaches (St-Pierre et al., 1998). The present study aimed to establish the presence of NPY Y(1) receptors on cultured hippocampal astrocytes using similar strategies. Immunocytochemical experiments were carried out using three antisera directed against distinct domains (amino acids sequence 185-203, 198-213 and 355-382) of the Y(1) receptor. Double-labeling experiments and confocal microscopy with these Y(1) receptor antisera demonstrated their recognition of the same sub-population (20%) of GFAP-positive astrocytes in culture. The immunostaining seen with all three Y(1) receptor antisera took the form of large irregular clusters distributed throughout cell bodies and processes. Further experiments using radioactive ligands confirmed the presence of NPY receptors on cultured hippocampal astrocytes. Emulsion receptor autoradiography using a newly developed ligand, [(125)I]GR231118 in the presence of PYY, hPP or BIBP3226 (1 microM), pharmacologically established the Y(1) nature of these receptors. Specific [(125)I]GR231118 binding was competed by PYY and the selective Y(1) antagonist BIBP3226 but not by hPP (a Y(4)/Y(5) agonist). Similar autoradiographic labeling patterns were obtained using [(125)I][Leu(31).Pro(34)]PYY (a Y(1)/Y(4)/Y(5) agonist) whereas [(125)I]PYY(3-36) (a Y(2)/Y(5) agonist) failed to generate any specific signal. Hence, rat cultured hippocampal astrocytes express a typical Y(1) receptor without evidence for the presence of Y(2), Y(4) or Y(5) subtypes. These data suggest a preferential regulation by NPY, acting via the Y(1) receptors, of astrocytic function.
利用放射受体分析和免疫组织化学方法,曾有研究报道培养的海马神经元上Y(1)亚型神经肽Y(NPY)受体的表达及药理学特性(St-Pierre等人,1998年)。本研究旨在采用类似策略确定培养的海马星形胶质细胞上是否存在NPY Y(1)受体。使用三种针对Y(1)受体不同结构域(氨基酸序列185 - 203、198 - 213和355 - 382)的抗血清进行免疫细胞化学实验。用这些Y(1)受体抗血清进行的双重标记实验和共聚焦显微镜检查表明,它们识别培养物中相同亚群(20%)的GFAP阳性星形胶质细胞。所有三种Y(1)受体抗血清所见的免疫染色呈大的不规则簇状,分布于整个细胞体和突起。使用放射性配体的进一步实验证实了培养的海马星形胶质细胞上存在NPY受体。在存在PYY、hPP或BIBP3226(1 microM)的情况下,使用新开发的配体[(125)I]GR231118进行乳剂受体放射自显影,从药理学上确定了这些受体的Y(1)性质。特异性[(125)I]GR231118结合可被PYY和选择性Y(1)拮抗剂BIBP3226竞争,但不能被hPP(一种Y(4)/Y(5)激动剂)竞争。使用[(125)I][Leu(31).Pro(34)]PYY(一种Y(1)/Y(4)/Y(5)激动剂)获得了类似的放射自显影标记模式,而[(125)I]PYY(3 - 36)(一种Y(2)/Y(5)激动剂)未能产生任何特异性信号。因此,大鼠培养的海马星形胶质细胞表达典型的Y(1)受体,没有证据表明存在Y(2)、Y(4)或Y(5)亚型。这些数据表明,NPY通过Y(1)受体对星形胶质细胞功能具有优先调节作用。