| Literature DB >> 31812242 |
Makoto Nakamura1, Hitoshi Yoshida2, Eri Takahashi1, Marcin Wlizla2, Kimiko Takebayashi-Suzuki1, Marko E Horb2, Atsushi Suzuki3.
Abstract
Xenopus tropicalis tadpoles can regenerate an amputated tail, including spinal cord, muscle and notochord, through cell proliferation and differentiation. However, the molecular mechanisms that regulate cell proliferation during tail regeneration are largely unknown. Here we show that JunB plays an important role in tail regeneration by regulating cell proliferation. The expression of junb is rapidly activated and sustained during tail regeneration. Knockout (KO) of junb causes a delay in tail regeneration and tissue differentiation. In junb KO tadpoles, cell proliferation is prevented before tissue differentiation. Furthermore, TGF-β signaling, which is activated just after tail amputation, regulates the induction and maintenance of junb expression. These findings demonstrate that JunB, a downstream component of TGF-β signaling, works as a positive regulator of cell proliferation during Xenopus tail regeneration.Entities:
Keywords: Cell proliferation; JunB; TGF-β signaling; Tissue differentiation; Xenopus tail regeneration
Mesh:
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Year: 2019 PMID: 31812242 PMCID: PMC6989358 DOI: 10.1016/j.bbrc.2019.11.060
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575