Cherdchu C, Hexum T D
Department of Pharmacology, University of Nebraska Medical Center, Omaha 68198-6260.
Neuropeptides. 1991 Aug;19(4):237-42. doi: 10.1016/0143-4179(91)90090-6.
Stimulation of chromaffin cells in culture with 1,1-dimethyl-4-phenylpiperazinium (DMPP) or depolarizing concentrations of K+ resulted in a significant secretion of high and low molecular weight enkephalin-like peptides (ELPs) into the culture medium. BioGel P-10 column chromatography was used to characterize the ELPs in chromaffin cell extracts and in culture media before and after stimulation with either DMPP or K+. DMPP (50 microM) stimulation produced a significant secretion of primarily low molecular weight (less than 3 kDa) ELPs whereas 56 mM K+ caused a secretion of both high and low molecular weights ELPs. The expected decrease in cellular content of low molecular weight peptides was not observed regardless of stimulation type. Our results support the hypothesis that the precursor/product ratio of secreted ELPs is dependent upon the nature of the chromaffin cell stimulus. Moreover the cellular content of low molecular weight ELPs is not depleted with either type of stimulation.
用1,1 - 二甲基 - 4 - 苯基哌嗪鎓(DMPP)或去极化浓度的K⁺刺激培养的嗜铬细胞,会导致高分子量和低分子量脑啡肽样肽(ELP)大量分泌到培养基中。采用BioGel P - 10柱色谱法对嗜铬细胞提取物以及用DMPP或K⁺刺激前后的培养基中的ELP进行表征。DMPP(50微摩尔)刺激主要导致低分子量(小于3千道尔顿)ELP的大量分泌,而56毫摩尔K⁺则引起高分子量和低分子量ELP的分泌。无论刺激类型如何,均未观察到低分子量肽细胞含量的预期下降。我们的结果支持这样的假设,即分泌的ELP的前体/产物比率取决于嗜铬细胞刺激的性质。此外,无论哪种类型的刺激,低分子量ELP的细胞含量都不会耗尽。