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时空控制的 cyclin D1 过表达可触发出生后小鼠内耳中超数细胞的产生。

Spatiotemporally controlled overexpression of cyclin D1 triggers generation of supernumerary cells in the postnatal mouse inner ear.

机构信息

Creighton University School of Dentistry, Dept. of Oral Biology, Omaha, NE, 68178, USA.

University of Nebraska-Lincoln, Dept. of Special Education and Communication Disorders, Lincoln, NE, 68583-0738, USA.

出版信息

Hear Res. 2020 May;390:107951. doi: 10.1016/j.heares.2020.107951. Epub 2020 Mar 19.

Abstract

The retinoblastoma family of pocket proteins (pRBs), composed of Rb1, p107, and p130 are negative regulators of cell-cycle progression. The deletion of any individual pRB in the auditory system triggers hair cells' (HCs) and supporting cells' (SCs) proliferation to different extents. Nevertheless, accessing their combined role in the inner ear through conditional or complete knockout methods is limited by the early mortality of the triple knockout. In quiescent cells, hyperphosphorylation and inactivation of the pRBs are maintained through the activity of the Cyclin-D1-cdk4/6 complex. Cyclin D1 (CycD1) is expressed in the embryonic and neonatal inner ear. In the mature organ of Corti (OC), CycD1 expression is significantly downregulated, paralleling the OC mitotic quiescence. Earlier studies showed that CycD1 overexpression leads to cell-cycle reactivation in cultures of inner ear explants. Here, we characterize a Cre-activated, Doxycycline (Dox)-controlled, conditional CycD1 overexpression model, which when bred to a tetracycline-controlled transcriptional activator and the Atoh1-cre mouse lines, allow for transient CycD1 overexpression and pRBs' downregulation in the inner ear in a reversible fashion. Analyses of postnatal mice's inner ears at various time points revealed the presence of supernumerary cells throughout the length of the cochlea and in the vestibular end-organs. Notably, most supernumerary cells were observed in the inner hair cells' (IHCs) region, expressed myosin VIIa (M7a), and showed no signs of apoptosis at any of the time points analyzed. Auditory and vestibular phenotypes were similar between the different genotypes and treatment groups. The fact that no significant differences were observed in auditory and vestibular function supports the notion that the supernumerary cells detected in the adult mice cochlea and macular end-organs may not impair auditory functions.

摘要

视网膜母细胞瘤家族的口袋蛋白(pRBs),由 Rb1、p107 和 p130 组成,是细胞周期进程的负调控因子。听觉系统中任何单个 pRB 的缺失都会在不同程度上触发毛细胞(HCs)和支持细胞(SCs)的增殖。然而,通过条件性或完全敲除方法来研究它们在内耳中的共同作用,受到三重敲除的早期死亡率的限制。在静止细胞中,pRBs 的高磷酸化和失活通过 Cyclin-D1-cdk4/6 复合物的活性来维持。Cyclin D1(CycD1)在胚胎和新生内耳中表达。在成熟的 Corti 器官(OC)中,CycD1 的表达显著下调,与 OC 的有丝分裂静止相一致。早期的研究表明,CycD1 的过表达会导致内耳外植体培养物中的细胞周期重新激活。在这里,我们描述了一种 Cre 激活、强力霉素(Dox)控制的条件性 CycD1 过表达模型,当与 tetracycline 控制的转录激活剂和 Atoh1-cre 小鼠系杂交时,该模型允许在内耳中以可逆的方式瞬时过表达 CycD1 和下调 pRBs。对不同时间点出生后小鼠内耳的分析显示,整个耳蜗和前庭终器中都存在多余的细胞。值得注意的是,大多数多余的细胞存在于内毛细胞(IHCs)区域,表达肌球蛋白 VIIa(M7a),并且在分析的任何时间点都没有凋亡的迹象。不同基因型和治疗组之间的听觉和前庭表型相似。在听觉和前庭功能方面没有观察到显著差异的事实支持这样一种观点,即在成年小鼠耳蜗和黄斑终器中检测到的多余细胞可能不会损害听觉功能。

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