Rabinovitch A, Suarez-Pinzon W L, Shi Y, Morgan A R, Bleackley R C
Department of Medicine, University of Alberta, Edmonton, Canada.
Diabetologia. 1994 Aug;37(8):733-8. doi: 10.1007/BF00404328.
The cytokines, interleukin 1, tumour necrosis factor, and interferon gamma are cytotoxic to islet beta cells, however, their mechanisms of beta-cell killing are not fully characterized. Since DNA damage is a mechanism of cytokine-induced cell death in some cell types, we sought evidence for cytotoxic effects of cytokines at a nuclear level in islet beta cells by measuring DNA fragmentation in rat islets and islet beta-cell lines. The individual cytokines, interleukin 1 (10 U/ml), tumour recrosis factor (10(3) U/ml) and interferon gamma (10(3) U/ml) inhibited insulin release from rat islets, but did not cause DNA fragmentation or destroy islet cells; by contrast, combination of the three cytokines induced DNA fragmentation and islet-cell death. Cytokine-induced DNA fragmentation preceded cell lysis in islet beta-cell lines (RINm5F, rat insulinoma cells; and NIT-1, NOD/Lt mouse transgenic beta cells), whereas in non-islet cell lines (GH-3, rat pituitary; and PC-12, rat adrenal) the cytokines induced cell lysis and no or late DNA fragmentation. Nicotinamide prevented both DNA fragmentation and destruction of RINm5F islet cells by the cytokines. These findings identify DNA as an early target of cytokine action in islet beta cells, and implicate DNA fragmentation as a mechanism of cytokine-induced beta-cell destruction.
细胞因子白细胞介素-1、肿瘤坏死因子和干扰素-γ对胰岛β细胞具有细胞毒性,然而,它们杀伤β细胞的机制尚未完全明确。由于DNA损伤是某些细胞类型中细胞因子诱导细胞死亡的一种机制,我们通过检测大鼠胰岛和胰岛β细胞系中的DNA片段化,来寻找细胞因子在胰岛β细胞核水平上的细胞毒性作用证据。单独的细胞因子,白细胞介素-1(10 U/ml)、肿瘤坏死因子(10³ U/ml)和干扰素-γ(10³ U/ml)可抑制大鼠胰岛释放胰岛素,但不会导致DNA片段化或破坏胰岛细胞;相比之下,这三种细胞因子联合使用则会诱导DNA片段化和胰岛细胞死亡。在胰岛β细胞系(RINm5F,大鼠胰岛素瘤细胞;和NIT-1,NOD/Lt小鼠转基因β细胞)中,细胞因子诱导的DNA片段化先于细胞裂解,而在非胰岛细胞系(GH-3,大鼠垂体;和PC-12,大鼠肾上腺)中,细胞因子诱导细胞裂解,且无DNA片段化或DNA片段化出现较晚。烟酰胺可防止细胞因子导致RINm5F胰岛细胞的DNA片段化和细胞破坏。这些发现确定DNA是细胞因子在胰岛β细胞中作用的早期靶点,并表明DNA片段化是细胞因子诱导β细胞破坏的一种机制。