Haller T, Dietl P, Deetjen P, Völkl H
Department of Physiology, University of Innsbruck, Austria.
Cell Calcium. 1996 Feb;19(2):157-65. doi: 10.1016/s0143-4160(96)90084-6.
To test for a possible role of lysosomes in intracellular Ca2+ homeostasis, the effects of glycyl-L-phenylalanine-beta-naphthylamide (GPN), known to permeabilize these organelles by osmotic swelling, were studied in single MDCK cells. Fluorescence of acridine orange, rhodol green dextran, lysotracker green and FITC-dextran indicated that GPN (0.2 mmol/l) elicited a reversible permeabilization of lysosomes. Cytosolic Ca2+ ([Ca2+]i) as determined by Fura-2 fluorescence increased from 60 +/- 11 to 534 +/- 66 nmol/l (n = 41) in the presence of GPN. Whereas only a single intracellular Ca2+ release could be induced by GPN in a Ca(2+)-free perfusate, repetitive release could be evoked in Ca2+ containing solutions suggesting reuptake of Ca2+ into lysosomal stores. GPN-induced Ca2+ release was blunted after pretreatment with thapsigargin (TG), an inhibitor of Ca(2+)-ATPase, or repeated applications of ATP inducing Ca2+ release from inositol trisphosphate (InsP3) sensitive Ca2+ stores. The effect of ATP on Ca2+ release was, however, not abolished by preceding GPN treatment. GPN-induced Ca2+ release from lysosomes was independent of InsP3 formation or Ca(2+)-induced Ca2+ release, since it was unaffected by the phospholipase C inhibitor U-73, 122 or by caffeine and ruthenium red. These results suggest that Ca2+ largely accumulates in lysosomal vesicles. Moreover, these organelles seem to be part or functionally coupled with InsP3-sensitive Ca2+ stores.
为了检测溶酶体在细胞内钙离子稳态中可能发挥的作用,我们在单个MDCK细胞中研究了甘氨酰-L-苯丙氨酸-β-萘酰胺(GPN)的作用,已知该物质可通过渗透肿胀使这些细胞器通透。吖啶橙、罗丹明绿葡聚糖、溶酶体示踪剂绿色荧光染料和异硫氰酸荧光素葡聚糖的荧光表明,GPN(0.2 mmol/l)可引起溶酶体的可逆通透。用Fura-2荧光测定的胞质钙离子浓度([Ca2+]i)在GPN存在下从60±11增加到534±66 nmol/l(n = 41)。在无钙灌注液中,GPN仅能诱导单次细胞内钙离子释放,而在含钙溶液中可诱发重复释放,提示钙离子可重新摄取到溶酶体储存中。在用毒胡萝卜素(TG,一种钙离子-ATP酶抑制剂)预处理或重复应用ATP诱导从三磷酸肌醇(InsP3)敏感的钙离子储存中释放钙离子后,GPN诱导的钙离子释放减弱。然而,先前的GPN处理并未消除ATP对钙离子释放的作用。GPN诱导的溶酶体钙离子释放与InsP3形成或钙离子诱导的钙离子释放无关,因为它不受磷脂酶C抑制剂U-73122或咖啡因及钌红的影响。这些结果表明,钙离子主要积聚在溶酶体囊泡中。此外,这些细胞器似乎是InsP3敏感的钙离子储存的一部分或在功能上与之耦合。