新しい方法で脳と内耳の形成過程を解明(New method reveals how the brain and inner ear are formed)

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2025-04-03 カロリンスカ研究所(KI)

新しい方法で脳と内耳の形成過程を解明(New method reveals how the brain and inner ear are formed)
Image of the inner ear. At the top, a dense mass of cells (blue) adjacent to the organ of hearing: a row of inner hair cells (blue, round) surrounded by supporting cells (purple and green diffuse squares). Then three rows of hair cells (large, blue, round), and then another row of supporting cells (smaller blue, round, inside squares). At the bottom, a dense mass of cells associated with the organ of hearing (circled in green). Photo: Sandra de Haan

スウェーデンのカロリンスカ研究所の研究チームは、マウス胚における神経系と内耳の形成過程を追跡する新手法を開発しました。幹細胞に遺伝的バーコードを導入することで、細胞がどのように分化し、脳や内耳の構造を形成するかを詳細に解析。この研究により、聴覚に重要な内耳の細胞が2種類の幹細胞由来であることが判明しました。成果は2025年『Science』に掲載され、将来の難聴治療や細胞再生医療への応用が期待されています。

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外胚葉バーコーディングによる神経と蝸牛のコンパートメント化の解明 Ectoderm barcoding reveals neural and cochlear compartmentalization

Sandra de Haan, Jingyan He, Agustin A. Corbat, Lenka Belicova, […], and Emma R. Andersson
Science  Published:3 Apr 2025

Editor’s summary

Sensory organs play a major role in how animals interact with the environment. de Haan et al. used in utero injection and lineage tracing to resolve cellular differentiation trajectories of the developing inner ear in mice. Lentiviral injection into the mouse amniotic cavity at embryonic day 7.5 allowed the authors to determine the various cell types within the cochlear epithelium, neural crest–derived glia, and intermediate cells in the cochlea. Their results led to the identification of cell types that were previously misclassified, and represent a comprehensive single-cell atlas of clonal relationships within the mouse cochlea. —Mattia Maroso

Abstract

Placodes and the neural crest are defining features of vertebrates. In this study, we investigate their lineages in mice using in utero approaches. We demonstrated that nanoinjection at embryonic day 7.5 targeted the ectoderm, including the future nervous system, placodes, and neural crest, allowing highly efficient manipulation of the future nervous system and inner ear. By using heritable DNA barcodes and high-throughput next-generation single-cell lineage tracing, we elucidated convergent differentiation pathways and identified distinct nervous system–, neural crest–, and otic placode–derived lineages. Clonal analyses identified early neural and cochlear compartmentalization, linking differentiated cell types to their progenitors or cellular siblings. This provides foundational insights for neuroscience and developmental biology.

医療・健康
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