The expression of NLRX1 in C57BL/6 mice cochlear hair cells: Possible relation to aging- and neomycin-induced deafness

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• 作者：Qianqian Yang^a ; ^b ; ¹ ; Gaoying Sun^a ; ^c ; ¹ ; Zhixin Cao^a ; ^b ; Haiyan Yin^a ; ^c ; Qi Qi^a ; ^c ; Jinghan Wang^a ; ^b ; Wenwen Liu^a ; ^c ; Xiaohui Bai^a ; ^c ; Haibo Wang^a ; ^c ; ^{wang.hb7585@hotmail.com" class="auth_mail" title="E-mail the corresponding author} ; Jianfeng Li^a ; ^b ; ^c ; ^{lijianfeng@hotmail.com" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Nucleotide-binding domain and leucine-rich-repeat-containing family member X1 ; NLRX1 ; C57BL/6 mice ; Hair cells ; Apoptosis
• 刊名：Neuroscience Letters
• 出版年：2016
• 出版时间：11 March 2016
• 年：2016
• 卷：616
• 期：Complete
• 页码：138-146
• 全文大小：3582 K

文摘

Nucleotide-binding domain and leucine-rich-repeat-containing family member X1 (NLRX1) is a cytoplasmic pattern recognition receptor that is predominantly located in mitochondria, which is tightly related to mitochondrial damage, reactive oxygen species (ROS) production, inflammation and apoptosis. The present study was designed to explore whether NLRX1 expresses in C57BL/6 mice cochlear hair cells and, if so, to investigate the possible correlations between NLRX1 and hearing. The location and dynamic expression of NLRX1 were investigated by immunofluorescence, real-time PCR and Western blotting. Hearing thresholds of C57BL/6 mice were measured by auditory brainstem response (ABR). Moreover, the downstream inflammatory and apoptotic pathways regulated by NLRX1 were examined in age-related and neomycin-induced hair cell damage. Data showed that NLRX1 expressed in cytoplasm of C57BL/6 cochlear hair cells, especially in the cilia, which were essential for sound sensation. The expression of NLRX1 in hair cells increased as the mice grew up, and, decreased as they aged. Additionally, the activated apoptotic JNK pathway was detected in 9-month old mice with worse-hearing and 3-month old mice treated with neomycin. Overall, results indicate that NLRX1 may relate to hair cell maturity, hearing formation and maintenance, and promote hair cell apoptosis through JNK pathway induced by aging and neomycin.