Literature DB >> 26963167

PARP-1-modulated AIF translocation is involved in streptomycin-induced cochlear hair cell death.

Yongdong Song1,2, Zhaomin Fan1, Xiaohui Bai2,3, Wenwen Liu2,3, Yuechen Han1, Lei Xu1, Mingming Wang1, Jianfeng Li2,3, Qingyin Zheng4, Daogong Zhang1, Haibo Wang1,2,3.   

Abstract

Conclusion SM-induced dose- and location-dependent cochlear hair cell death in vitro. AIF might be translocated from mitochondria to nucleus and cytoplasm within SM-treated hair cells. The translocation of AIF might be modulated by PARP-1. Objective Streptomycin (SM), one of the widely used aminoglycoside nowadays, is still causing significant permanent sensorineural hearing loss owing to sensory hair cell death. This study was designed to investigate the role of apoptosis-inducing factor (AIF), an important mitochondrial cell death regulator, in SM ototoxicity within neonatal rat cochleae and HEI-OC1 cells. Methods The viability of HEI-OC1 cells was quantified by MTT assay. AIF, PARP-1, and myosin VIIa distributions were achieved by immunofluorescence. mRNA and protein expression of AIF and PARP-1 were examined by q-PCR and Western-blot. Results The hair cell loss was concomitant with the SM concentration variation, and aggravated from apical to basal turn. AIF was detected in nuclear region and AIF mRNA was up-regulated after SM incubation. Besides, AIF protein expression in mitochondria was decreased, whereas in cytosol it was increased. PARP-1 mRNA and protein were also up-regulated. 3-AB could attenuate the cell death and reverse the changes of AIF distribution by blocking PARP-1.

Entities:  

Keywords:  HEI-OC1 cell; Streptomycin ototoxicity; cochleae organotypic culture; programmed cell death

Mesh:

Substances:

Year:  2016        PMID: 26963167      PMCID: PMC4861077          DOI: 10.3109/00016489.2016.1143968

Source DB:  PubMed          Journal:  Acta Otolaryngol        ISSN: 0001-6489            Impact factor:   1.494


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2.  Aminoglycosides rapidly inhibit NAD(P)H metabolism increasing reactive oxygen species and cochlear cell demise.

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