Metz S A, Dunlop M
Research Service, Denver VA Medical Center, CO 80220.
Biochem J. 1990 Sep 1;270(2):427-35. doi: 10.1042/bj2700427.
Although exogenous phosphatidic acid (PA) has been shown to promote insulin release, the effects of endogenous PA on endocrine function are largely unexplored. In order to generate PA in situ, intact adult-rat islets were treated with exogenous phospholipases of the D type (PLD), and their effects on phospholipid metabolism and on insulin release were studied in parallel. Chromatographically purified PLD from Streptomyces chromofuscus stimulated the accumulation of PA in [14C]arachidonate- or [14C]myristate-prelabelled islets, and also promoted insulin secretion over an identical concentration range. During 30 min incubations, insulin release correlated closely with the accumulation of [14C]arachidonate-labelled PA (r2 = 0.98; P less than 0.01) or [14C]myristate-labelled PA (r2 = 0.97; P less than 0.01). Similar effects were seen both in freshly isolated and in overnight-cultured intact islets. In contrast, PLDs (from cabbage or peanut) which do not support phospholipid hydrolysis at the pH of the extracellular medium also did not promote insulin release. The effects on secretion of the active PLD preparation were inhibited by modest cooling (to 30 degrees C); dantrolene or Co2+ also inhibited PLD-induced secretion without decreasing PLD-induced PA formation. Additionally, the removal of PLD left the subsequent islet responsiveness to glucose intact, further supporting an exocytotic non-toxic mechanism. PLD-induced insulin release did not appear to require influx of extracellular Ca2+, nor could the activation of protein kinase C clearly be implicated. During incubations of 30 min, PLD selectively generated PA; however, more prolonged incubations (60 min) also led to production of some diacyglycerol and free arachidonic acid concomitant with progressive insulin release. These data suggest that PLD activation has both rapid and direct effects (via PA) and more delayed, secondary, effects (via other effects of PA or the generation of other lipid signals). Taken in conjunction with our demonstration that pancreatic islets contain an endogenous PLD which generates PA [Dunlop & Metz (1989) Biochem. Biophys. Res. Commun. 163, 922-928], these studies provide evidence suggesting that PLD activation (and possibly other pathways leading to PA formation) could play a role in stimulus-secretion coupling in pancreatic islets.
尽管外源性磷脂酸(PA)已被证明可促进胰岛素释放,但内源性PA对内分泌功能的影响在很大程度上尚未得到探索。为了原位生成PA,用D型外源性磷脂酶(PLD)处理完整的成年大鼠胰岛,并同时研究其对磷脂代谢和胰岛素释放的影响。从暗褐链霉菌经色谱纯化的PLD刺激了[14C]花生四烯酸或[14C]肉豆蔻酸预标记胰岛中PA的积累,并且在相同浓度范围内也促进了胰岛素分泌。在30分钟的孵育过程中,胰岛素释放与[14C]花生四烯酸标记的PA的积累密切相关(r2 = 0.98;P小于0.01)或与[14C]肉豆蔻酸标记的PA的积累密切相关(r2 = 0.97;P小于0.01)。在新鲜分离的和过夜培养的完整胰岛中均观察到类似的效果。相反,在细胞外培养基的pH值下不支持磷脂水解的PLD(来自卷心菜或花生)也不促进胰岛素释放。适度冷却(至30摄氏度)可抑制活性PLD制剂对分泌的影响;丹曲林或Co2 +也抑制PLD诱导的分泌,而不降低PLD诱导的PA形成。此外,去除PLD后,胰岛随后对葡萄糖的反应性保持完整,进一步支持了一种胞吐无毒机制。PLD诱导的胰岛素释放似乎不需要细胞外Ca2 +的流入,蛋白激酶C的激活也不明显。在30分钟的孵育过程中,PLD选择性地生成PA;然而,更长时间的孵育(60分钟)也导致一些二酰基甘油和游离花生四烯酸的产生,同时胰岛素逐渐释放。这些数据表明,PLD激活具有快速和直接的作用(通过PA)以及更延迟的、次要的作用(通过PA的其他作用或其他脂质信号的产生)。结合我们的证明,即胰岛含有一种可生成PA的内源性PLD [邓洛普和梅茨(1989年)生物化学与生物物理研究通讯163,922 - 928],这些研究提供了证据表明PLD激活(以及可能导致PA形成的其他途径)可能在胰岛的刺激 - 分泌偶联中起作用。