Tesoriere Annachiara, Ghirardo Rachele, Terrin Francesca, Sernesi Francesco, Meneghetti Giacomo, Dalla Valle Luisa, Dinarello Alberto, Argenton Francesco
Department of Biology, University of Padova, Padua, Italy.
Present address: Novo Nordisk Foundation Center for Stem Cell Medicine (reNEW), University of Copenhagen, Copenhagen DK-2200, Denmark.
Int J Biol Sci. 2025 Jan 1;21(1):271-284. doi: 10.7150/ijbs.96400. eCollection 2025.
Stat3 is a transcription factor with a key role in cell proliferation and migration. Using the zebrafish line we showed that the genetic ablation results in a marked decrease of tail fin regrowth, demonstrating that this transcription factor is fundamental in the regeneration process. Stat3 activity is finely modulated by post-translational modifications that occur in several residues of the protein (i.e., Y705 and S727 phosphorylation), with tissue-specific effects. Using the newly generated zebrafish line, we demonstrated that the Stat3 phosphorylation in the non-canonical S751 site (homologous of mammalian serine 727) is required for the regeneration of tail fin in both larval and adult stage, even if this phosphorylation has largely been reported to have marginal roles in Stat3 activity. Our analysis showed that both and mutant zebrafish lines have alterations in the expression of genes involved in epithelial and bone tissue regeneration, including genes coding for the vitamin D signaling pathway. Interestingly, the reduced regeneration activity in zebrafish and larvae is partially rescued by vitamin D treatment. Together, these results reveal a Stat3-vitamin D co-regulatory mechanism during zebrafish tail fin regeneration.
信号转导和转录激活因子3(Stat3)是一种在细胞增殖和迁移中起关键作用的转录因子。利用斑马鱼品系,我们发现基因敲除会导致尾鳍再生显著减少,这表明该转录因子在再生过程中至关重要。Stat3的活性受到蛋白质几个残基(即Y705和S727磷酸化)发生的翻译后修饰的精细调节,具有组织特异性效应。利用新构建的斑马鱼品系,我们证明了非经典S751位点(与哺乳动物丝氨酸727同源)的Stat3磷酸化在幼体和成体阶段的尾鳍再生中都是必需的,尽管据报道这种磷酸化在Stat3活性中作用不大。我们的分析表明,两种突变斑马鱼品系中参与上皮和骨组织再生的基因表达都有改变,包括编码维生素D信号通路的基因。有趣的是,维生素D处理可部分挽救斑马鱼幼体中再生活性的降低。这些结果共同揭示了斑马鱼尾鳍再生过程中的Stat3-维生素D共同调节机制。