Islam M S, Kindmark H, Larsson O, Berggren P O
Rolf Luft Center for Diabetes Research, Department of Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
Biochem J. 1997 Jan 15;321 ( Pt 2)(Pt 2):347-54. doi: 10.1042/bj3210347.
2,2'-Dithiodipyridine (2,2'-DTDP), a reactive disulphide that mobilizes Ca2+ from ryanodine-sensitive Ca2+ stores in muscle, induced a biphasic increase in cytoplasmic free Ca2+ concentration ([Ca2+]i) in pancreatic beta-cells loaded with fura 2. This increase consisted of an early transient followed by a second, slower, rise. The [Ca2+]i transient was dependent on extracellular Ca2+ and disappeared on treatment with nimodipine. The reactive disulphide caused plasma membrane depolarization, as studied by the perforated-patch configuration of the patch-clamp technique. Hence membrane depolarization and opening of the L-type voltage-gated Ca2+ channels were responsible for the first transient in [Ca2+]i. The second slower increase in [Ca2+]i was prolonged but readily reversed by the disulphide-reducing agent 1,4-dithiothreitol. This increase in [Ca2+]i was not decreased by nimodipine or by omission of extracellular Ca2+, but was eliminated when the Ins(1,4,5)P3-sensitive Ca2+ pool was first depleted by carbachol. Ryanodine or its beta-alanyl analogue did not release Ca2+ from intracellular stores, and a high concentration of ryanodine did not inhibit Ca2+ release by 2,2'-DTDP. The disulphide compound suppressed glucose metabolism and decreased the mitochondrial inner-membrane potential. We conclude that thiol oxidation by 2,2'-DTDP affects Ca2+ homeostasis in beta-cells by multiple mechanisms. However, unlike the situation in muscle, in beta-cells 2,2'-DTDP releases Ca2+ from intracellular pools by mechanisms that do not involve activation of ryanodine receptors. Instead, in these cells the Ins(1,4,5)P3-sensitive intracellular Ca2+ store comprises an alternative target for the Ca(2+)-mobilizing action of the reactive disulphide compound.
2,2'-二硫代二吡啶(2,2'-DTDP)是一种活性二硫化物,可从肌肉中对兰尼碱敏感的钙储存库中动员钙离子,它使装载了fura 2的胰腺β细胞中的细胞质游离钙离子浓度([Ca2+]i)出现双相增加。这种增加包括一个早期的短暂升高,随后是第二个较慢的升高。[Ca2+]i的短暂升高依赖于细胞外钙离子,并且在用尼莫地平处理后消失。如通过膜片钳技术的穿孔膜片配置所研究的,这种活性二硫化物导致质膜去极化。因此,膜去极化和L型电压门控钙离子通道的开放是[Ca2+]i的第一个短暂升高的原因。[Ca2+]i的第二个较慢的升高持续时间较长,但可被二硫化物还原剂1,4-二硫苏糖醇迅速逆转。[Ca2+]i的这种升高不受尼莫地平或细胞外钙离子缺失的影响,但当用卡巴胆碱首先耗尽Ins(1,4,5)P3敏感的钙池时,这种升高就会消除。兰尼碱或其β-丙氨酰类似物不会从细胞内储存库中释放钙离子,并且高浓度的兰尼碱不会抑制2,2'-DTDP引起的钙离子释放。这种二硫化物化合物抑制葡萄糖代谢并降低线粒体内膜电位。我们得出结论,2,2'-DTDP引起的硫醇氧化通过多种机制影响β细胞中的钙离子稳态。然而,与肌肉中的情况不同,在β细胞中,2,2'-DTDP通过不涉及兰尼碱受体激活的机制从细胞内储存库中释放钙离子。相反,在这些细胞中,Ins(1,4,5)P3敏感的细胞内钙储存库是这种活性二硫化物化合物动员钙离子作用的另一个靶点。