An eGFP-Col4a2 mouse model reveals basement membrane dynamics underlying hair follicle morphogenesis.

IF 7.4 1区 生物学 Q1 CELL BIOLOGY Journal of Cell Biology Pub Date : 2025-02-03 Epub Date: 2024-12-10 DOI:10.1083/jcb.202404003
Duligengaowa Wuergezhen, Eleonore Gindroz, Ritsuko Morita, Kei Hashimoto, Takaya Abe, Hiroshi Kiyonari, Hironobu Fujiwara
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Abstract

Precisely controlled remodeling of the basement membrane (BM) is crucial for morphogenesis, but its molecular and tissue-level dynamics, underlying mechanisms, and functional significance in mammals remain largely unknown due to limited visualization tools. We developed mouse lines in which the endogenous collagen IV gene (Col4a2) was fused with a fluorescent tag. Through live imaging of developing hair follicles, we reveal a spatial gradient in the turnover rate of COL4A2 that is closely coupled with both the BM expansion rate and the proliferation rate of epithelial progenitors. Epithelial progenitors are displaced with directionally expanding BMs but do not actively migrate on stationary BM. The addition of a matrix metalloproteinase inhibitor delays COL4A2 turnover, restrains BM expansion, and increases perpendicular divisions of epithelial progenitors, altering hair follicle morphology. Our findings highlight the spatially distinct dynamics of BM and their key roles in orchestrating progenitor cell behavior and organ shape during development.

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精确控制基底膜(BM)的重塑对形态发生至关重要,但由于可视化工具有限,哺乳动物基底膜的分子和组织水平动态、潜在机制和功能意义在很大程度上仍不为人所知。我们开发了内源性胶原蛋白 IV 基因(Col4a2)与荧光标签融合的小鼠品系。通过对发育中的毛囊进行实时成像,我们发现 COL4A2 的周转率存在空间梯度,这种梯度与 BM 的扩张率和上皮祖细胞的增殖率密切相关。上皮祖细胞会随着定向扩张的基质移动,但不会在静止的基质上主动迁移。添加基质金属蛋白酶抑制剂可延缓 COL4A2 的周转,抑制 BM 的扩张,增加上皮祖细胞的垂直分裂,从而改变毛囊形态。我们的研究结果突显了基质金属酶在空间上的不同动态及其在发育过程中协调祖细胞行为和器官形态的关键作用。
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来源期刊
Journal of Cell Biology
Journal of Cell Biology 生物-细胞生物学
CiteScore
12.60
自引率
2.60%
发文量
213
审稿时长
1 months
期刊介绍: The Journal of Cell Biology (JCB) is a comprehensive journal dedicated to publishing original discoveries across all realms of cell biology. We invite papers presenting novel cellular or molecular advancements in various domains of basic cell biology, along with applied cell biology research in diverse systems such as immunology, neurobiology, metabolism, virology, developmental biology, and plant biology. We enthusiastically welcome submissions showcasing significant findings of interest to cell biologists, irrespective of the experimental approach.
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