In vivo partial reprogramming of myofibers promotes muscle regeneration by remodeling the stem cell niche.
Chao WangRuben Rabadan RosPaloma Martinez-RedondoZaijun MaLei ShiYuan XueIsabel Guillen-GuillenLing HuangTomoaki HishidaHsin-Kai LiaoNúñez-Delicado EstrellaConcepcion Rodriguez EstebanPedro Guillen-GarciaPradeep ReddyJuan Carlos Izpisua BelmontePublished in: Nature communications (2021)
Short-term, systemic expression of the Yamanaka reprogramming factors (Oct-3/4, Sox2, Klf4 and c-Myc [OSKM]) has been shown to rejuvenate aging cells and promote tissue regeneration in vivo. However, the mechanisms by which OSKM promotes tissue regeneration are unknown. In this work, we focus on a specific tissue and demonstrate that local expression of OSKM, specifically in myofibers, induces the activation of muscle stem cells or satellite cells (SCs), which accelerates muscle regeneration in young mice. In contrast, expressing OSKM directly in SCs does not improve muscle regeneration. Mechanistically, expressing OSKM in myofibers regulates the expression of genes important for the SC microenvironment, including upregulation of p21, which in turn downregulates Wnt4. This is critical because Wnt4 is secreted by myofibers to maintain SC quiescence. Thus, short-term induction of the Yamanaka factors in myofibers may promote tissue regeneration by modifying the stem cell niche.
Keyphrases
- stem cells
- poor prognosis
- skeletal muscle
- induced apoptosis
- cell therapy
- cell cycle arrest
- binding protein
- cell proliferation
- long non coding rna
- gene expression
- transcription factor
- optical coherence tomography
- mesenchymal stem cells
- bone marrow
- diabetic retinopathy
- magnetic resonance imaging
- endoplasmic reticulum stress
- sensitive detection
- contrast enhanced
- drug induced