Institute of Molecular Biology, Hannover Medical School, Hannover, Germany.
Medical Biology, Amsterdam Reproduction & Development, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
Nat Commun. 2022 Dec 9;13(1):7628. doi: 10.1038/s41467-022-35214-4.
The auditory function of the mammalian cochlea relies on two types of mechanosensory hair cells and various non-sensory supporting cells. Recent studies identified the transcription factors INSM1 and IKZF2 as regulators of outer hair cell (OHC) fate. However, the transcriptional regulation of the differentiation of inner hair cells (IHCs) and their associated inner supporting cells (ISCs) has remained enigmatic. Here, we show that the expression of the transcription factor TBX2 is restricted to IHCs and ISCs from the onset of differentiation until adulthood and examine its function using conditional deletion and misexpression approaches in the mouse. We demonstrate that TBX2 acts in prosensory progenitors as a patterning factor by specifying the inner compartment of the sensory epithelium that subsequently gives rise to IHCs and ISCs. Hair cell-specific inactivation or misexpression causes transdifferentiation of hair cells indicating a cell-autonomous function of TBX2 in inducing and maintaining IHC fate.
哺乳动物耳蜗的听觉功能依赖于两种类型的机械感觉毛细胞和各种非感觉支持细胞。最近的研究确定了转录因子 INSM1 和 IKZF2 是外毛细胞 (OHC) 命运的调节因子。然而,内毛细胞 (IHC) 和其相关的内支持细胞 (ISC) 的分化的转录调控仍然是个谜。在这里,我们显示转录因子 TBX2 的表达局限于从分化开始到成年的 IHCs 和 ISCs,并使用条件缺失和在小鼠中的异位表达方法来研究其功能。我们证明 TBX2 在祖细胞中作为一个模式形成因子发挥作用,通过特化随后产生 IHCs 和 ISCs 的感觉上皮的内区室。毛细胞特异性失活或异位表达导致毛细胞的转分化,表明 TBX2 在诱导和维持 IHC 命运中具有细胞自主功能。