Stachura M E, Lapp C A, Tyler J M, Lee Y S
Department of Medicine, Veterans Administration Medical Center, Augusta, Georgia.
In Vitro Cell Dev Biol. 1990 May;26(5):482-92. doi: 10.1007/BF02624090.
We previously documented both the spontaneous acceleration of growth hormone (GH) and prolactin (PRL) production by GH3 cells during perifusion and the suppression of their production during plate culture. We here present the role played by medium flow itself in this differential behavior. Increasing rates of perifusion flow (pump rates of 1 to 5 ml/h, equivalent to chamber flow rates of 0.19 to 1.3 microliters.min-1.mm-2 of cross-sectional area) were associated with enhanced GH and PRL secretion. Flow rate-dependent basal hormone secretion rates were established quickly and were stable for the first 10 to 14 h of perifusion. The previously documented independent, spontaneous, and continuously accelerating production of both hormones that followed during the subsequent 40 (PRL) to 60 (GH) h of perifusion was also shown to be flow-rate related. Any time the rate of medium flow was changed within an experiment, the rate of hormone secretion was modulated. However, that modulation did not interrupt ongoing flow-associated acceleration of hormone production once the latter had begun. In addition, GH3 cell product(s) from one cell column reversibly inhibited secretion from cells in a downstream column. The inhibition did not occur when cells in the downstream column had been exposed to trypsin. Other work had suggested that neither GH, PRL, insulinlike growth factor-I, leucine, nor nutrient exhaustion were responsible for the effect. These data are consistent with autocrine-paracrine feedback regulation of GH3 cells by a secretory product(s). Feedback would thus provide a mechanism to effect flow-rate-dependent modulation of GH and PRL release, and to explain accelerating hormone production during perifusion.
我们之前记录了在灌流过程中GH3细胞生长激素(GH)和催乳素(PRL)分泌的自发加速以及平板培养过程中它们分泌的抑制。我们在此展示了培养基流动本身在这种差异行为中所起的作用。灌流流速增加(泵速为1至5毫升/小时,相当于腔室流速为0.19至1.3微升·分钟⁻¹·毫米⁻²横截面积)与GH和PRL分泌增强相关。流速依赖性基础激素分泌率迅速建立,并在灌流的最初10至14小时内保持稳定。在随后灌流的40(PRL)至60(GH)小时内之前记录的两种激素独立、自发且持续加速的分泌也显示与流速有关。在实验过程中,每当培养基流速发生变化时,激素分泌速率就会受到调节。然而,一旦激素分泌加速开始,这种调节不会中断正在进行的与流动相关的激素分泌加速。此外,来自一个细胞柱的GH3细胞产物可逆地抑制下游柱中细胞的分泌。当下游柱中的细胞暴露于胰蛋白酶时,这种抑制不会发生。其他研究表明,GH、PRL、胰岛素样生长因子-I、亮氨酸或营养物质耗尽均与这种效应无关。这些数据与GH3细胞通过一种分泌产物进行自分泌-旁分泌反馈调节一致。因此,反馈将提供一种机制来实现对GH和PRL释放的流速依赖性调节,并解释灌流过程中激素分泌加速的现象。