During embryogenesis, cells self-organize into precise patterns that enable tissues and organs to acquire specialized functions. Despite its importance, the molecular choreography driving these collective cellular behaviors remains poorly understood, posing a major challenge in developmental biology and limiting progress in regenerative medicine. Here, we use the developing mouse hair follicle as a model mini-organ to investigate the early events of epithelial bud formation. We identify the Rho GTPase regulator ARHGEF3 as a critical upstream factor that restricts cell fate acquisition and establishes a radial gradient of P-cadherin across the placode during early hair follicle development. In Arhgef3 knockout embryos, placodes are enlarged and exhibit elevated P-cadherin levels at cell-cell junctions, disrupting gradient formation without affecting E-cadherin distribution. This defect correlates with aberrant epithelial organization and increased incidence of straight hair follicle downgrowth. Our findings position ARHGEF3 as a novel regulator of cadherin patterning and placode polarization, and suggest broader roles in the morphogenesis of other epithelial appendages governed by similar developmental programs.
The Rho GTPase regulator ARHGEF3 orchestrates hair placode budding by coordinating cell fate and P-cadherin patterning in mice.
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作者:Kalyanakrishnan Krithika, Beaudin Amy, Jetté Alexandra, Ghezelbash Sarah, Ioana Hotea Diana, Chen Jie, Lefrançois Philippe, Laurin Mélanie
| 期刊: | PLoS Biology | 影响因子: | 7.200 |
| 时间: | 2026 | 起止号: | 2026 Jan 5; 24(1):e3003572 |
| doi: | 10.1371/journal.pbio.3003572 | ||
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