Checler F, Mazella J, Kitabgi P, Vincent J P
J Neurochem. 1986 Dec;47(6):1742-8. doi: 10.1111/j.1471-4159.1986.tb13083.x.
The present article describes the interaction of neurotensin with specific receptors in pure primary cultured neurons and the mechanisms by which this peptide is inactivated by these cells. Neurotensin binding sites are not detectable in nondifferentiated neurons and appear during maturation. The binding at 37 degrees C of [monoiodo-Tyr3]neurotensin to monolayers of neurons 96 h after plating is saturable and characterized by a dissociation constant of 300 pM and a maximal binding capacity of 178 fmol/mg of protein. The binding parameters as well as the specificity of these receptors toward neurotensin analogues reveal close similarities between the binding sites present in primary cultured neurons and those described in other membrane preparations or cells. Neurotensin is rapidly degraded by primary cultured neurons. The sites of primary inactivating cleavages are the Pro7-Arg8, Arg8-Arg9, and Pro10-Tyr11 bonds. Proline endopeptidase is totally responsible for the cleavage at the Pro7-Arg8 bond and contributes to the hydrolysis mainly at the Pro10-Tyr11 site. However, the latter breakdown is also generated by a neurotensin-degrading neutral metallopeptidase. The cleavage at the Arg8-Arg9 bond is due to a peptidase that can be specifically inhibited by N-[1(R,S)-carboxy-2-phenylethyl]-alanyl-alanyl-phenylalanyl-p- aminobenzoate. The secondary processing occurring on neurotensin degradation products are: a bestatin-sensitive aminopeptidasic conversion of neurotensin11-13 to free Tyr11, and a rapid cleavage of neurotensin8-13 by proline endopeptidase. A model for the inactivation of neurotensin in primary cultured neurons is proposed and compared to that previously described for purified rat brain synaptic membranes.
本文描述了神经降压素与纯原代培养神经元中特定受体的相互作用,以及该肽被这些细胞灭活的机制。在未分化的神经元中检测不到神经降压素结合位点,其在成熟过程中出现。接种96小时后,[单碘酪氨酸3]神经降压素在37℃下与神经元单层的结合是可饱和的,解离常数为300 pM,最大结合容量为178 fmol/mg蛋白质。这些受体的结合参数以及对神经降压素类似物的特异性表明,原代培养神经元中的结合位点与其他膜制剂或细胞中描述的结合位点非常相似。神经降压素被原代培养神经元迅速降解。主要灭活切割位点是Pro7-Arg8、Arg8-Arg9和Pro10-Tyr11键。脯氨酸内肽酶完全负责Pro7-Arg8键的切割,主要在Pro10-Tyr11位点促进水解。然而,后者的分解也由一种神经降压素降解中性金属肽酶产生。Arg8-Arg9键的切割是由于一种肽酶,其可被N-[1(R,S)-羧基-2-苯乙基]-丙氨酰-丙氨酰-苯丙氨酰-对氨基苯甲酸特异性抑制。神经降压素降解产物上发生的二次加工包括:神经降压素11-13被一种对亮抑酶肽敏感的氨肽酶转化为游离的Tyr11,以及脯氨酸内肽酶对神经降压素8-13的快速切割。本文提出了原代培养神经元中神经降压素失活的模型,并与先前描述的纯化大鼠脑突触膜模型进行了比较。