Mammalian Genetics Unit, MRC Harwell Institute, Oxfordshire, UK.
Department of Otorhinolaryngology Head and Neck Surgery, University of Maryland School of Medicine, Baltimore, MD, USA.
Nature. 2018 Nov;563(7733):696-700. doi: 10.1038/s41586-018-0728-4. Epub 2018 Nov 21.
The sensory cells that are responsible for hearing include the cochlear inner hair cells (IHCs) and outer hair cells (OHCs), with the OHCs being necessary for sound sensitivity and tuning. Both cell types are thought to arise from common progenitors; however, our understanding of the factors that control the fate of IHCs and OHCs remains limited. Here we identify Ikzf2 (which encodes Helios) as an essential transcription factor in mice that is required for OHC functional maturation and hearing. Helios is expressed in postnatal mouse OHCs, and in the cello mouse model a point mutation in Ikzf2 causes early-onset sensorineural hearing loss. Ikzf2 OHCs have greatly reduced prestin-dependent electromotile activity, a hallmark of OHC functional maturation, and show reduced levels of crucial OHC-expressed genes such as Slc26a5 (which encodes prestin) and Ocm. Moreover, we show that ectopic expression of Ikzf2 in IHCs: induces the expression of OHC-specific genes; reduces the expression of canonical IHC genes; and confers electromotility to IHCs, demonstrating that Ikzf2 can partially shift the IHC transcriptome towards an OHC-like identity.
负责听觉的感觉细胞包括耳蜗内毛细胞 (IHCs) 和外毛细胞 (OHCs),OHCs 对于声音敏感性和调谐是必需的。两种细胞类型都被认为来自共同的祖细胞;然而,我们对控制 IHC 和 OHC 命运的因素的理解仍然有限。在这里,我们确定 Ikzf2(编码 Helios)是小鼠中一种必需的转录因子,它是 OHC 功能成熟和听力所必需的。Helios 在出生后小鼠的 OHCs 中表达,在 cello 小鼠模型中,Ikzf2 的点突变导致早发性感觉神经性听力损失。Ikzf2 OHCs 的 prestin 依赖性电活动大大减少,这是 OHC 功能成熟的标志,并且表现出关键的 OHC 表达基因如 Slc26a5(编码 prestin)和 Ocm 的水平降低。此外,我们还表明,在 IHC 中异位表达 Ikzf2:诱导 OHC 特异性基因的表达;降低经典 IHC 基因的表达;并赋予 IHC 电活动,表明 Ikzf2 可以部分将 IHC 转录组向 OHC 样特征转移。