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首页> 外文期刊>PLoS One >Gene Expression Analysis of Forskolin Treated Basilar Papillae Identifies MicroRNA181a as a Mediator of Proliferation
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Gene Expression Analysis of Forskolin Treated Basilar Papillae Identifies MicroRNA181a as a Mediator of Proliferation

机译:Forskolin处理的基底乳头的基因表达分析确定MicroRNA181a作为增殖的介质。

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Background Auditory hair cells spontaneously regenerate following injury in birds but not mammals. A better understanding of the molecular events underlying hair cell regeneration in birds may allow for identification and eventually manipulation of relevant pathways in mammals to stimulate regeneration and restore hearing in deaf patients. Methodology/Principal Findings Gene expression was profiled in forskolin treated (i.e., proliferating) and quiescent control auditory epithelia of post-hatch chicks using an Affymetrix whole-genome chicken array after 24 (n = 6), 48 (n = 6), and 72 (n = 12) hours in culture. In the forskolin-treated epithelia there was significant (p0.05; two-fold change) upregulation of many genes thought to be relevant to cell cycle control and inner ear development. Gene set enrichment analysis was performed on the data and identified myriad microRNAs that are likely to be upregulated in the regenerating tissue, including microRNA181a (miR181a), which is known to mediate proliferation in other systems. Functional experiments showed that miR181a overexpression is sufficient to stimulate proliferation within the basilar papilla, as assayed by BrdU incorporation. Further, some of the newly produced cells express the early hair cell marker myosin VI, suggesting that miR181a transfection can result in the production of new hair cells. Conclusions/Significance These studies have identified a single microRNA, miR181a, that can cause proliferation in the chicken auditory epithelium with production of new hair cells.
机译:背景鸟类受伤后,听觉毛发细胞会自发再生,而哺乳动物则不会。更好地了解鸟类毛细胞再生背后的分子事件可能有助于鉴定并最终操纵哺乳动物中的相关途径,以刺激聋患者的再生并恢复听力。方法/主要发现在24(n = 6),48(n = 6)和(24)(n = 6)的条件下,使用Affymetrix全基因组鸡阵列分析了经福斯科林处理(即增殖)和静止控制后听觉上皮的雏鸡的基因表达。培养72(n = 12)小时。在用福司高林处理的上皮细胞中,许多与细胞周期控制和内耳发育有关的基因均显着上调(p <0.05;变化两倍)。对数据进行了基因集富集分析,并鉴定了可能在再生组织中上调的无数microRNA,包括已知在其他系统中介导增殖的microRNA181a(miR181a)。功能实验表明,通过BrdU掺入,miR181a过表达足以刺激基底乳头内的增殖。此外,一些新产生的细胞表达早期毛细胞标记物肌球蛋白VI,表明miR181a转染可导致新毛细胞的产生。结论/意义这些研究已经鉴定出单个microRNA miR181a,它可以在鸡的听觉上皮细胞中增殖并产生新的毛细胞。

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