Abstract

ObjectiveThis research aimed to investigate whether glutamate induced spiral ganglion neurons (SGNs) apoptosis through apoptosis inducing factor (AIF) pathway. And verify whether PD150606, a calpain inhibitor could prevent apoptosis by inhibiting cleaving and releasing AIF in mitochondrion.MethodsSGNs of postnatal days 0-3 were harvested and cultured in dishes. 20 mM Glu, the caspase inhibitor Z-VAD-FMK and calpain inhibitor PD150606 were added into cultured dishes separately. We used optical microscope and immunofluoresence staining to observe cell morphology and AIF distribution, RT-PCR and Westernblot to analyse AIF and calpain expression in SGNs. TUNEL assay was used to test cell apoptosis.ResultsCell morphology and nuclear translocation of AIF were altered in SGNs by 20 mM Glu treated in vitro. The axon of SGN shortened, more apoptosis SGN were observed and the expression of AIF and calpain were up-regulated in Glu-treated group than the normal one (P<0.05). The same experiments were conducted in 20 mM+PD150606 treated group and 20 mM+Z-VAD-FMK group. Obviously AIF were located from cytoplasm to the nuclear and the expressions of AIF and calpain were down-regulated by PD150606 (P<0.05). Positive cells in TUNEL staining decreased after PD150606 treating. However, Z-VAD-FMK had no influence on AIF, calpain expression or cell apoptosis.ConclusionThe AIF-related apoptosis pathway is involved in the process of Glu-induced SGN injury. Furthermore, the inhibition of calpain can prevent AIF from releasing the nuclear or inducing SGN apoptosis.

Highlights

  • Apoptosis inducing factor (AIF) plays a key role in the process of cell apoptosis, as an AIF-related apoptosis pathway[1]

  • Cell morphology and nuclear translocation of AIF were altered in SGNs by 20 mM Glu treated in vitro

  • AIF were located from cytoplasm to the nuclear and the expressions of AIF and calpain were down-regulated by PD150606 (P

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Summary

Introduction

Apoptosis inducing factor (AIF) plays a key role in the process of cell apoptosis, as an AIF-related apoptosis pathway[1]. AIF is a mitochondrial inter-membrane flavo-protein that can be released from mitochondrion to nucleus to induce chromatin condensation and large-scale DNA fragmentation[3,4]. In addition to its binding to DNA, AIF is a redox enzyme, which plays a role in nicotinamide adenine dinucleotide (NADH) oxidase[5]. The NADH oxidase activity of AIF is separable from its DNA-binding activity to induce apoptosis. It could cleave AIF to mature in mitochondrion and release mature AIF through permeability transition pore (PTP) to nucleus inducing cell apoptosis[7]. Calpain could be repressed to cleave AIF by PD150606 binding to the calcium site[3]

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