希少疾患研究を前進させる「ミニ胃」培養モデルを開発 (Lab-grown mini-stomachs could boost understanding of rare diseases)

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2026-01-25 ユニバーシティ・カレッジ・ロンドン(UCL)

英ロンドン大学ユニバーシティ・カレッジ(UCL)の研究チームは、**培養した「ミニ胃(胃オルガノイド)」**を用いて、希少疾患の理解と治療研究を進展させる可能性を示した。ヒト幹細胞から作製されたミニ胃は、実際の胃組織に近い構造と機能を持ち、従来の動物実験では再現が困難だった遺伝性消化管疾患や発達異常を詳細に解析できる。研究では、特定の遺伝子変異を持つ患者由来細胞からミニ胃を作成し、疾患に特有の細胞異常や発生過程の乱れを可視化することに成功した。これにより、病態メカニズムの解明だけでなく、将来的には個別化医療や新規治療法・薬剤評価への応用が期待される。ミニ臓器技術は、希少疾患研究における重要な実験基盤となる可能性を示している。

<関連情報>

機能的胃壁成熟および前庭部小窩過形成の患者特異的モデリングのためのヒト胃多領域アセンブロイド Human gastric multi-regional assembloids for functional parietal maturation and patient-specific modelling of antral foveolar hyperplasia

Brendan C. Jones,Giada Benedetti,Giuseppe Calà,Ramin Amiri,Lucinda Tullie,Roberto Lutman,Jahangir Sufi,Lucy Holland,Daniyal J. Jafree,Monika Balys,Glenn Anderson,Ian C. Simcock,Owen J. Arthurs,Simon Eaton,Nicola Elvassore,Vivian SW Li,Christopher J. Tape,Kelsey DJ Jones,Camilla Luni,Giovanni Giuseppe Giobbe & Paolo De Coppi
Nature Biomedical Engineering  Published:23 January 2026
DOI:https://doi.org/10.1038/s41551-025-01553-y

希少疾患研究を前進させる「ミニ胃」培養モデルを開発 (Lab-grown mini-stomachs could boost understanding of rare diseases)

Abstract

Patient-derived human organoids have the capacity to self-organize into more complex structures. However, to what extent gastric organoids can recapitulate differentiated cell types and mucosal functions remains unexplored. Here we report on how region-specific gastric organoids can self-assemble into complex multi-regional assembloids. These assembloids show increased complexity and cross-communication between different gastric regions, allowing for the emergence of the elusive parietal cell type that is responsible for the production of gastric acid and shows a functional response to drugs targeting the H+/K+ ATPase pump. We generate assembloids from paediatric patients with a genetic condition found to be associated with unusual antral foveolar hyperplasia and hyperplastic polyposis. Our multi-regional assembloid efficiently recapitulates hyperplastic-like antral regions, with decreased mucin secretion and glycosylated H+/K+ ATPase subunit beta, which results in impaired gastric acid secretion. Multi-regional gastric assembloids, generated using paediatric-stem-cell-derived organoids, successfully recapitulate the structural and functional characteristics of the human stomach, offering a promising tool for studying gastric epithelial interactions and disease mechanisms that were previously challenging to investigate in primary models.

細胞遺伝子工学
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