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在一个综合征小鼠模型中揭示的中耳鼓泡大小、空洞缺陷与慢性中耳炎之间的相互关系。

The interconnected relationships between middle ear bulla size, cavitation defects, and chronic otitis media revealed in a syndromic mouse model.

作者信息

Fons Juan M, Milmoe Natalie J, Dack Michael R G, Joshi Leena, Thompson Hannah, Tucker Abigail S

机构信息

Centre for Craniofacial and Regenerative Biology, Fl27 Guy's Hospital, King's College London, London, United Kingdom.

出版信息

Front Genet. 2022 Oct 10;13:933416. doi: 10.3389/fgene.2022.933416. eCollection 2022.

Abstract

High incidence of chronic otitis media is associated with human craniofacial syndromes, suggesting that defects in the formation of the middle ear and associated structures can have a knock-on effect on the susceptibility to middle ear inflammation. Patients with branchio-oto-renal (BOR) syndrome have several defects in the ear leading to both sensorineural and conductive hearing loss, including otitis media. 40% of BOR syndrome cases are due to haploinsufficiency, with mouse models affecting , mimicking many of the defects found in patients. Here, we characterize the onset, consequences, and underlying causes of chronic otitis media in heterozygous mice. Cavitation defects were evident in these mice from postnatal day (P)11 onwards, with mesenchyme around the promontory and attic regions of the middle ear space. This mesenchyme was still prominent in adult heterozygous mice, while the wild-type littermates had fully aerated ears from P14 onwards. MicroCT analysis highlighted a significantly smaller bulla, confirming the link between bulla size defects and the ability of the mesenchyme to retract successfully. Otitis media was observed from P14, often presenting unilaterally, resulting in hyperplasia of the middle ear mucosa, expansion of secretory cells, defects in the motile cilia, and changes in basal epithelial cell markers. A high incidence of otitis media was identified in older mice but only associated with ears with retained mesenchyme. To understand the impact of the environment, the mouse line was rederived onto a super-clean environment. Cavitation defects were still evident at early stages, but these generally resolved over time, and importantly, no signs of otitis media were observed at 6 weeks. In conclusion, we show that a small bulla size is closely linked to defects in cavitation and the presence of retained mesenchyme. A delay in retraction of the mesenchyme predates the onset of otitis media, making the ears susceptible to its development. Early exposure to OM appears to exacerbate the cavitation defect, with mesenchyme evident in the middle ear throughout the animal's life. This highlights that permanent damage to the middle ear can arise as a consequence of the early onset of OM.

摘要

慢性中耳炎的高发病率与人类颅面综合征相关,这表明中耳及相关结构形成过程中的缺陷可能会对中耳炎症易感性产生连锁反应。鳃耳肾(BOR)综合征患者的耳部存在多种缺陷,导致感音神经性和传导性听力损失,包括中耳炎。40%的BOR综合征病例是由于单倍剂量不足引起的,小鼠模型也有类似情况,模拟了患者中发现的许多缺陷。在这里,我们描述了杂合小鼠慢性中耳炎的发病、后果及潜在原因。从出生后第(P)11天起,这些小鼠的中耳腔出现明显的空化缺陷,中耳腔岬部和上鼓室区域周围有间充质。这种间充质在成年杂合小鼠中仍然很明显,而野生型同窝小鼠从P14开始耳朵就完全充气了。显微CT分析突出显示鼓室显著变小,证实了鼓室大小缺陷与间充质成功退缩能力之间的联系。从P14开始观察到中耳炎,通常单侧出现,导致中耳黏膜增生、分泌细胞扩张、活动纤毛缺陷以及基底上皮细胞标志物的变化。在老年小鼠中发现中耳炎的高发病率,但仅与间充质残留的耳朵有关。为了解环境的影响,将小鼠品系重新培育到超清洁环境中。早期仍明显有空化缺陷,但这些缺陷通常会随着时间的推移而解决,重要的是,在6周时未观察到中耳炎迹象。总之,我们表明鼓室小与空化缺陷和间充质残留有关。间充质退缩延迟早于中耳炎的发病,使耳朵易患中耳炎。早期接触中耳炎似乎会加剧空化缺陷,在动物的整个生命过程中,中耳都有明显的间充质。这突出表明中耳炎的早期发病可能导致中耳的永久性损伤。

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