Fiory Francesca, Parrillo Luca, Raciti Gregory Alexander, Zatterale Federica, Nigro Cecilia, Mirra Paola, Falco Roberta, Ulianich Luca, Di Jeso Bruno, Formisano Pietro, Miele Claudia, Beguinot Francesco
Dipartimento di Scienze Mediche e Traslazionali dell'Università di Napoli "Federico II", Naples, Italy; URT dell'Istituto di Endocrinologia e Oncologia Sperimentale Gaetano Salvatore, Consiglio Nazionale delle Ricerche, Naples, Italy.
Dipartimento di Scienze e Tecnologie Biologiche e Ambientali, Università del Salento, Lecce, Italy.
PLoS One. 2014 Dec 9;9(12):e113655. doi: 10.1371/journal.pone.0113655. eCollection 2014.
The small scaffold protein PED/PEA-15 is involved in several different physiologic and pathologic processes, such as cell proliferation and survival, diabetes and cancer. PED/PEA-15 exerts an anti-apoptotic function due to its ability to interfere with both extrinsic and intrinsic apoptotic pathways in different cell types. Recent evidence shows that mice overexpressing PED/PEA-15 present larger pancreatic islets and increased beta-cells mass. In the present work we investigated PED/PEA-15 role in hydrogen peroxide-induced apoptosis in Ins-1E beta-cells. In pancreatic islets isolated from Tg(PED/PEA-15) mice hydrogen peroxide-induced DNA fragmentation was lower compared to WT islets. TUNEL analysis showed that PED/PEA-15 overexpression increases the viability of Ins-1E beta-cells and enhances their resistance to apoptosis induced by hydrogen peroxide exposure. The activity of caspase-3 and the cleavage of PARP-1 were markedly reduced in Ins-1E cells overexpressing PED/PEA-15 (Ins-1E(PED/PEA-15)). In parallel, we observed a decrease of the mRNA levels of pro-apoptotic genes Bcl-xS and Bad. In contrast, the expression of the anti-apoptotic gene Bcl-xL was enhanced. Accordingly, DNA fragmentation was higher in control cells compared to Ins-1E(PED/PEA-15) cells. Interestingly, the preincubation with propranolol, an inhibitor of the pathway of PLD-1, a known interactor of PED/PEA-15, responsible for its deleterious effects on glucose tolerance, abolishes the antiapoptotic effects of PED/PEA-15 overexpression in Ins-1E beta-cells. The same results have been obtained by inhibiting PED/PEA-15 interaction with PLD-1 in Ins-1E(PED/PEA-15). These results show that PED/PEA-15 overexpression is sufficient to block hydrogen peroxide-induced apoptosis in Ins-1E cells through a PLD-1 mediated mechanism.
小支架蛋白PED/PEA-15参与多种不同的生理和病理过程,如细胞增殖与存活、糖尿病和癌症。PED/PEA-15具有抗凋亡功能,因为它能够在不同细胞类型中干扰外源性和内源性凋亡途径。最近的证据表明,过表达PED/PEA-15的小鼠胰岛更大,β细胞质量增加。在本研究中,我们调查了PED/PEA-15在过氧化氢诱导的Ins-1Eβ细胞凋亡中的作用。在从Tg(PED/PEA-15)小鼠分离的胰岛中,过氧化氢诱导的DNA片段化低于野生型胰岛。TUNEL分析表明,PED/PEA-15过表达增加了Ins-1Eβ细胞的活力,并增强了它们对过氧化氢暴露诱导的凋亡的抗性。在过表达PED/PEA-15的Ins-1E细胞(Ins-1E(PED/PEA-15))中,caspase-3的活性和PARP-1的切割明显降低。同时,我们观察到促凋亡基因Bcl-xS和Bad的mRNA水平下降。相反,抗凋亡基因Bcl-xL的表达增强。因此,与Ins-1E(PED/PEA-15)细胞相比,对照细胞中的DNA片段化更高。有趣的是,用普萘洛尔(一种PLD-1途径的抑制剂,PLD-1是PED/PEA-15的已知相互作用因子,对葡萄糖耐量有有害影响)预孵育,消除了PED/PEA-15过表达在Ins-1Eβ细胞中的抗凋亡作用。通过抑制Ins-1E(PED/PEA-15)中PED/PEA-15与PLD-1的相互作用也得到了相同的结果。这些结果表明,PED/PEA-15过表达足以通过PLD-1介导的机制阻断过氧化氢诱导的Ins-1E细胞凋亡。