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工程化上皮曲率控制肠类器官中潘氏细胞的定位。

Engineered epithelial curvature controls Paneth cell localization in intestinal organoids.

作者信息

Yavitt F Max, Khang Alex, Bera Kaustav, McNally Delaney L, Blatchley Michael R, Gallagher Aaron P, Klein Ophir D, Castillo-Azofeifa David, Dempsey Peter J, Anseth Kristi S

机构信息

Department of Chemical and Biological Engineering, University of Colorado Boulder, Boulder, CO, 80303, USA.

BioFrontiers Institute, University of Colorado Boulder, Boulder, CO, 80303, USA.

出版信息

Cell Biomater. 2025 Apr 22;1(3). doi: 10.1016/j.celbio.2025.100046. Epub 2025 Apr 7.

Abstract

The cellular organization within organoid models is important to regulate tissue specific function, yet few engineering approaches can control or direct cellular organization. Here, a photodegradable hydrogel is used to create softened regions that direct crypt formation within intestinal organoids, where the dimensions of the photosoftened regions generate predictable and defined crypt architectures. Guided by metrics of crypt morphology, this photopatterning method is used to control the width and length of organoid crypts, which ultimately defines the curvature of the epithelium. By tracking expression of differentiated Paneth cell markers in real-time, we show that epithelial curvature directs the localization of Paneth cells within engineered crypts, providing user-directed control over organoid functionality. We anticipate that our improved control over organoid architecture and thus Paneth cell localization will lead to more consistent organoid models for both mechanistic studies and translational applications.

摘要

类器官模型中的细胞组织对于调节组织特定功能很重要,但很少有工程方法能够控制或引导细胞组织。在这里,一种可光降解的水凝胶被用于创建软化区域,这些区域可引导肠道类器官内隐窝的形成,其中光软化区域的尺寸可产生可预测且明确的隐窝结构。在隐窝形态指标的指导下,这种光图案化方法被用于控制类器官隐窝的宽度和长度,这最终决定了上皮细胞的曲率。通过实时追踪分化的潘氏细胞标志物的表达,我们发现上皮细胞曲率可引导潘氏细胞在工程化隐窝内的定位,从而为用户提供对类器官功能的定向控制。我们预计,我们对类器官结构以及潘氏细胞定位的更好控制,将为机制研究和转化应用带来更一致的类器官模型。

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