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Denervation Drives YAP/TAZ Activation in Muscular Fibro/Adipogenic Progenitors.


ABSTRACT: Loss of motoneuron innervation (denervation) is a hallmark of neurodegeneration and aging of the skeletal muscle. Denervation induces fibrosis, a response attributed to the activation and expansion of resident fibro/adipogenic progenitors (FAPs), i.e., multipotent stromal cells with myofibroblast potential. Using in vivo and in silico approaches, we revealed FAPs as a novel cell population that activates the transcriptional coregulators YAP/TAZ in response to skeletal muscle denervation. Here, we found that denervation induces the expression and transcriptional activity of YAP/TAZ in whole muscle lysates. Using the PdgfraH2B:EGFP/+ transgenic reporter mice to trace FAPs, we demonstrated that denervation leads to increased YAP expression that accumulates within FAPs nuclei. Consistently, re-analysis of published single-nucleus RNA sequencing (snRNA-seq) data indicates that FAPs from denervated muscles have a higher YAP/TAZ signature level than control FAPs. Thus, our work provides the foundations to address the functional role of YAP/TAZ in FAPs in a neurogenic pathological context, which could be applied to develop novel therapeutic approaches for the treatment of muscle disorders triggered by motoneuron degeneration.

SUBMITTER: Gallardo FS 

PROVIDER: S-EPMC10059792 | biostudies-literature | 2023 Mar

REPOSITORIES: biostudies-literature

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Denervation Drives YAP/TAZ Activation in Muscular Fibro/Adipogenic Progenitors.

Gallardo Felipe S FS   Córdova-Casanova Adriana A   Bock-Pereda Alexia A   Rebolledo Daniela L DL   Ravasio Andrea A   Casar Juan Carlos JC   Brandan Enrique E  

International journal of molecular sciences 20230315 6


Loss of motoneuron innervation (denervation) is a hallmark of neurodegeneration and aging of the skeletal muscle. Denervation induces fibrosis, a response attributed to the activation and expansion of resident fibro/adipogenic progenitors (FAPs), i.e., multipotent stromal cells with myofibroblast potential. Using in vivo and in silico approaches, we revealed FAPs as a novel cell population that activates the transcriptional coregulators YAP/TAZ in response to skeletal muscle denervation. Here, w  ...[more]

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