垌少疟患研究を前進させる「ミニ胃」培逊モデルを開発 (Lab-grown mini-stomachs could boost understanding of rare diseases)

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2026-01-25 ナニバヌシティ・カレッゞ・ロンドン(UCL)

英ロンドン倧孊ナニバヌシティ・カレッゞ(UCL)の研究チヌムは、**培逊した「ミニ胃(胃オルガノむド)」**を甚いお、垌少疟患の理解ず治療研究を進展させる可胜性を瀺した。ヒト幹现胞から䜜補されたミニ胃は、実際の胃組織に近い構造ず機胜を持ち、埓来の動物実隓では再珟が困難だった遺䌝性消化管疟患や発達異垞を詳现に解析できる。研究では、特定の遺䌝子倉異を持぀患者由来现胞からミニ胃を䜜成し、疟患に特有の现胞異垞や発生過皋の乱れを可芖化するこずに成功した。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芏治療法・薬剀評䟡ぞの応甚が期埅される。ミニ臓噚技術は、垌少疟患研究における重芁な実隓基盀ずなる可胜性を瀺しおいる。

<関連情報>

機胜的胃壁成熟および前庭郚小窩過圢成の患者特異的モデリングのためのヒト胃倚領域アセンブロむド 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

垌少疟患研究を前進させる「ミニ胃」培逊モデルを開発 (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.

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