An ERK-dependent molecular switch antagonizes fibrosis and promotes regeneration in spiny mice (Acomys)

Autor(en): Tomasso, Antonio
Koopmans, Tim
Lijnzaad, Philip
Bartscherer, Kerstin 
Seifert, Ashley W.
Stichwörter: ACTIVATION; CANCER; CELLS; DISCOVERY; INHIBITOR; Multidisciplinary Sciences; Science & Technology - Other Topics; SET ENRICHMENT ANALYSIS; STEM; THERAPIES; TRANSCRIPTION; TRANSITION
Erscheinungsdatum: 2023
Herausgeber: AMER ASSOC ADVANCEMENT SCIENCE
Enthalten in: SCIENCE ADVANCES
Band: 9
Ausgabe: 17
Zusammenfassung: 
Although most mammals heal injured tissues and organs with scarring, spiny mice (Acomys) naturally regenerate skin and complex musculoskeletal tissues. Now, the core signaling pathways driving mammalian tissue regeneration are poorly characterized. Here, we show that, while immediate extracellular signal-regulated kinase (ERK) activation is a shared feature of scarring (Mus) and regenerating (Acomys) injuries, ERK activity is only sustained at high levels during complex tissue regeneration. Following ERK inhibition, ear punch regeneration in Acomys shifted toward fibrotic repair. Using single-cell RNA sequencing, we identified ERK-responsive cell types. Loss-and gain-of-function experiments prompted us to uncover fibroblast growth factor and ErbB signaling as upstream ERK regulators of regeneration. The ectopic activation of ERK in scar-prone injuries induced a pro-regenerative response, including cell proliferation, extracellular matrix remodeling, and hair follicle neogenesis. Our data detail an important distinction in ERK activity between regenerating and poorly regenerating adult mammals and open avenues to redirect fibrotic repair toward regenerative healing.
ISSN: 2375-2548
DOI: 10.1126/sciadv.adf2331

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