Jadot M, Biélande V, Beauloye V, Wattiaux-De Coninck S, Wattiaux R
Laboratoire de Chimie Physiologique, Facultés Universitaires Notre-Dame de la Paix, Namur, Belgium.
Biochim Biophys Acta. 1990 Aug 24;1027(2):205-9. doi: 10.1016/0005-2736(90)90086-4.
Glycyl-D-phenylalanine-2-naphthylamide (Gly-D-Phe-2-NNap) is a cytotoxic agent as exemplified by its effect on Vero cells in culture. This effect is inhibited to some extent by nigericin. On the other hand, Gly-D-Phe-2-NNap induces an increase of free activity of N-acetylglucosaminidase when incubated with a mitochondrial fraction of rat liver at pH 7.5. The phenomenon is inhibited by chloroquine, NH4Cl and nigericin, substances that are known to increase the intralysosomal pH. The latency of enzymes located in other subcellular structures - mitochondria, peroxisomes and endoplasmic reticulum - is not affected by Gly-D-Phe-2-NNap. Moreover, that compound does not cause a release of FITC-Dextran present in endosomes. Apparently Gly-D-Phe-2-NNap is a specific lytic agent for lysosomes. It is proposed that the molecule behaves like a lysosomotropic substance that is able to attack the lysosomal membrane from the interior of the organelle. Its cytotoxic properties could be explained by its effect on lysosomes.
甘氨酰-D-苯丙氨酸-2-萘酰胺(Gly-D-Phe-2-NNap)是一种细胞毒性剂,其对培养的Vero细胞的作用即为例证。尼日利亚菌素在一定程度上抑制了这种作用。另一方面,当在pH 7.5条件下与大鼠肝脏线粒体部分一起孵育时,Gly-D-Phe-2-NNap会诱导N-乙酰葡糖胺酶的游离活性增加。该现象受到氯喹、NH4Cl和尼日利亚菌素的抑制,这些物质已知会提高溶酶体内的pH值。位于其他亚细胞结构(线粒体、过氧化物酶体和内质网)中的酶的潜伏性不受Gly-D-Phe-2-NNap的影响。此外,该化合物不会导致内体中存在的FITC-葡聚糖释放。显然,Gly-D-Phe-2-NNap是一种针对溶酶体的特异性裂解剂。有人提出该分子的行为类似于一种溶酶体亲和性物质,能够从细胞器内部攻击溶酶体膜。其细胞毒性特性可以通过其对溶酶体的作用来解释。