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Updated: Feb 25, 2026

Volumetric Imaging and Analysis of Primary Cilia in Musculoskeletal Tissue using the ARL13B-CENTRIN-2 Mouse Model
Published on: March 28, 2025
Cilia Control Fat Deposition during Tissue Repair
Eusebio Perdiguero1, Antonio L Serrano1, Pura Muñoz-Cánoves2
1Department of Experimental and Health Sciences, Pompeu Fabra University (UPF), CIBER on Neurodegenerative Diseases (CIBERNED), E-08003 Barcelona, Spain.
Primary cilia guide the fate of fibro/adipogenic progenitors (FAPs) in muscle regeneration. These cellular structures promote fat cell development by inhibiting Hedgehog signaling in injured muscle.
Area of Science:
- Muscle regeneration
- Cell biology
- Stem cell differentiation
Background:
- Fibro/adipogenic progenitors (FAPs) are key cells in skeletal muscle repair, influencing fibrous and fat tissue formation.
- The precise mechanisms controlling FAP differentiation into adipocytes or fibrocytes during regeneration are still being elucidated.
Purpose of the Study:
- To investigate the role of primary cilia in directing the differentiation of FAPs during skeletal muscle regeneration.
- To determine how primary cilia influence the balance between fat and fibrous tissue deposition in injured muscle.
Main Methods:
- Utilized mouse models of muscle injury and disease.
- Employed techniques to visualize and analyze primary cilia in FAPs.
- Investigated the impact of primary cilia on Hedgehog signaling pathways.
Main Results:
- Primary cilia were found to be present and functional in FAPs within injured and diseased muscle tissue.
- The presence of primary cilia was correlated with an increased propensity for FAPs to differentiate into adipocytes (fat cells).
- Primary cilia were shown to restrain Hedgehog signaling, a known inhibitor of adipogenesis.
Conclusions:
- Primary cilia act as critical regulators of FAP fate during skeletal muscle regeneration.
- By inhibiting Hedgehog signaling, primary cilia promote the adipogenic differentiation of FAPs, contributing to fat deposition.
- These findings offer new insights into the cellular mechanisms governing muscle repair and tissue remodeling.
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