Melcangi R C, Galbiati M, Messi E, Piva F, Martini L, Motta M
Department of Endocrinology, University of Milan, Italy.
Endocrinology. 1995 Feb;136(2):679-86. doi: 10.1210/endo.136.2.7835301.
The possible existence of a humoral communication between glial cells and LHRH-secreting neurons has been studied using the LHRH-secreting GT1-1 cell line and type 1 astrocytes. Two different designs have been adopted: 1) GT1-1 cells were coincubated with purified cultures of type 1 rat astrocytes, and 2) GT1-1 cells were exposed to the conditioned medium (CM) in which type 1 rat astrocytes had been grown for 24 h. LHRH was measured by RIA in the medium of the GT1-1 cell cultures at different time intervals. The data show that short periods (1, 3, and 6 h) of either coculture or exposure to previously frozen CM significantly increase the release of LHRH from the GT1-1 cells. However, more prolonged times of coculture (e.g. 2 and 5 days) or exposure to CM (e.g. 48 h) induce a significant decrease in the amount of LHRH in the medium. The stimulatory effect on LHRH release appears to be specific for type 1 astrocytes (either cortical or hypothalamic), because neither the CM of oligodendrocytes nor the CM of LNCaP cells (a cell line derived from a human prostatic cancer) possess stimulating activities. Heating the type 1 astrocyte-CM to 100 C for 10 min does not eliminate the ability of the CM to significantly increase the release of LHRH from GT1-1 cells at 1, 3, and 6 h. Because of the opposite effects encountered in the short and long term experiments, it was hypothesized that the CM might contain, in addition to LHRH-releasing principle(s), LHRH-degrading properties. Known amounts of standard LHRH were then added to type 1 astrocyte-CM, either untreated or submitted to heating at 100 C for 10 min. The amount of LHRH added to untreated CM decreases progressively; on the contrary, the amount of LHRH added to heated CM remains unchanged. These results confirm that one or more heat-sensitive enzymes able to degrade LHRH may be present in the type 1 astrocyte-CM. As previously mentioned, the experiments reported so far were performed using type 1 astrocyte-CM that had been kept frozen for various periods of time, before being tested for its LHRH-releasing activity. Surprisingly, fresh CM proves to be inactive, whereas heated CM is effective; this suggests that the factor involved might be activated by the two opposite experimental procedures.(ABSTRACT TRUNCATED AT 400 WORDS)
利用分泌促性腺激素释放激素(LHRH)的GT1-1细胞系和1型星形胶质细胞,对神经胶质细胞与分泌LHRH的神经元之间可能存在的体液通讯进行了研究。采用了两种不同的设计:1)将GT1-1细胞与纯化培养的1型大鼠星形胶质细胞共同培养,2)将GT1-1细胞暴露于1型大鼠星形胶质细胞已在其中生长24小时的条件培养基(CM)中。在不同时间间隔,通过放射免疫分析(RIA)测定GT1-1细胞培养基中的LHRH。数据表明,短期(1、3和6小时)的共培养或暴露于先前冷冻的CM中,可显著增加GT1-1细胞中LHRH的释放。然而,更长时间的共培养(如2天和5天)或暴露于CM(如48小时)会导致培养基中LHRH量显著减少。对LHRH释放的刺激作用似乎对1型星形胶质细胞(皮质或下丘脑的)具有特异性,因为少突胶质细胞的CM和LNCaP细胞(源自人类前列腺癌的细胞系)的CM均不具有刺激活性。将1型星形胶质细胞-CM加热至100℃ 10分钟,并不会消除CM在1、3和6小时显著增加GT1-1细胞释放LHRH的能力。由于在短期和长期实验中遇到相反的效应,推测CM除了含有LHRH释放因子外,可能还具有LHRH降解特性。然后将已知量的标准LHRH添加到未处理或在100℃加热10分钟的1型星形胶质细胞-CM中。添加到未处理CM中的LHRH量逐渐减少;相反,添加到加热CM中的LHRH量保持不变。这些结果证实,1型星形胶质细胞-CM中可能存在一种或多种能够降解LHRH的热敏感酶。如前所述,到目前为止报道的实验是使用在测试其LHRH释放活性之前已冷冻不同时间段的1型星形胶质细胞-CM进行的。令人惊讶的是,新鲜CM被证明无活性,而加热的CM是有效的;这表明所涉及的因子可能被这两种相反的实验程序激活。(摘要截短至400字)