foxm1 Modulates Cell Non-Autonomous Response in Zebrafish Skeletal Muscle Homeostasis.
Fábio J FerreiraLeonor CarvalhoElsa LogarinhoJosé BessaPublished in: Cells (2021)
foxm1 is a master regulator of the cell cycle, contributing to cell proliferation. Recent data have shown that this transcription factor also modulates gene networks associated with other cellular mechanisms, suggesting non-proliferative functions that remain largely unexplored. In this study, we used CRISPR/Cas9 to disrupt foxm1 in the zebrafish terminally differentiated fast-twitching muscle cells. foxm1 genomic disruption increased myofiber death and clearance. Interestingly, this contributed to non-autonomous satellite cell activation and proliferation. Moreover, we observed that Cas9 expression alone was strongly deleterious to muscle cells. Our report shows that foxm1 modulates a muscle non-autonomous response to myofiber death and highlights underreported toxicity to high expression of Cas9 in vivo.
Keyphrases
- skeletal muscle
- crispr cas
- cell cycle
- cell proliferation
- genome editing
- induced apoptosis
- transcription factor
- poor prognosis
- cell cycle arrest
- single cell
- cell therapy
- signaling pathway
- oxidative stress
- copy number
- insulin resistance
- endoplasmic reticulum stress
- cell death
- metabolic syndrome
- pi k akt
- stem cells
- electronic health record
- long non coding rna
- binding protein
- type diabetes
- dna methylation
- machine learning
- big data
- artificial intelligence