From sebocytes to skin engineering human sebaceous organoids within a reconstructed dermal matrix.

IF 5.1 Q2 TOXICOLOGY
Frontiers in toxicology Pub Date : 2026-07-31 eCollection Date: 2026-01-01 DOI:10.3389/ftox.2026.1874806
Tommaso Pusceddu, Luna Ardondi, Maria Pia Cavaleri, Lucia Sileo, Ilaria Vitali, Camila Quezada Meza, Michele Massironi, Marco Massironi, Barbara Zavan
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引用次数: 0

Abstract

Introduction: Sebaceous gland biology depends on the integration of lipid metabolism, tissue architecture, and stromal interactions, yet most available in vitro systems fail to capture these features simultaneously. This work reports the generation of a functional three-dimensional (3D) sebaceous gland organoid embedded within a matrix and designed to reproduce the structural and functional properties of native sebaceous tissue.

Methods: Using SZ95 sebocytes, we first established baseline responses in monolayer conditions using linoleic acid (LA) stimulation and pharmacological inhibition with retinol (RTN) and capsaicin (CPS). We then reconstructed a 3D organoid model in which a sebocyte-rich lipidogenic compartment was spatially organized within a matrix-supported microenvironment and associated with an outer stromal-like component. The model was evaluated using morphological, ultrastructural, and immunofluorescence analyses. To further define the mode of action of sebogenic activation in 3D, we analyzed genes related to extracellular matrix remodeling and tissue adaptation.

Results: In both monolayer and 3D models, LA successfully induced a sebogenic program, characterized by increased lipid accumulation and upregulation of PPARγ and FABP4, which was effectively attenuated by RTN and CPS. The 3D model successfully maintained essential compartmentalization, epithelial identity, and stromal organization. Furthermore, transcriptional analysis revealed that LA stimulation in 3D induced coordinated changes in extracellular matrix and basement membrane genes (including MMP13, MMP16, and THBS2), indicating that sebogenesis is directly coupled with structural remodeling and microenvironmental adaptation.

Conclusion: Altogether, these results demonstrate that we successfully reconstructed a functional in vitro model of a sebaceous gland organoid and established this platform as a relevant tool for mechanistic studies and for cosmetic screening of compounds targeting sebum regulation and sebaceous gland dysfunction.

从皮脂细胞到皮肤工程,重建真皮基质内的人类皮脂类器官。
皮脂腺生物学取决于脂质代谢、组织结构和基质相互作用的整合,然而大多数可用的体外系统无法同时捕获这些特征。本研究报告了嵌入在基质中的功能性三维(3D)皮脂腺类器官的生成,并设计用于再现天然皮脂腺组织的结构和功能特性。方法:利用SZ95皮脂细胞,我们首先通过亚油酸(LA)刺激和视黄醇(RTN)和辣椒素(CPS)的药理抑制,在单层条件下建立基线反应。然后,我们重建了一个三维类器官模型,其中富含脂细胞的脂质室在空间上组织在基质支持的微环境中,并与外部基质样成分相关。采用形态学、超微结构和免疫荧光分析对模型进行评价。为了进一步确定增脂激活的3D作用模式,我们分析了与细胞外基质重塑和组织适应相关的基因。结果:在单层和3D模型中,LA成功诱导了一个增脂程序,其特征是脂质积累增加,PPARγ和FABP4上调,RTN和CPS有效减弱。3D模型成功地维持了基本的区隔化、上皮身份和基质组织。此外,转录分析显示,3D LA刺激诱导细胞外基质和基底膜基因(包括MMP13、MMP16和THBS2)的协同变化,表明油脂生成与结构重塑和微环境适应直接相关。结论:我们成功构建了皮脂腺类器官的体外功能模型,并为皮脂调节和皮脂腺功能障碍靶向化合物的机制研究和化妆品筛选建立了平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.80
自引率
0.00%
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审稿时长
13 weeks
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