Department of Ecological Developmental Adaptability Life Sciences, Graduate School of Life Sciences, Tohoku University, Aobayama Aoba-ku, Sendai, 980-8578, Japan.
Laboratory of Molecular and Developmental Biology, National Institute of Genetics, Mishima, Shizuoka, 411-8540, Japan; Department of Genetics, The Graduate University for Advanced Studies, SOKENDAI, Mishima, Shizuoka, 411-8540, Japan.
Dev Biol. 2020 Jul 15;463(2):110-123. doi: 10.1016/j.ydbio.2020.04.010. Epub 2020 May 16.
We show for the first time endoskeletal regeneration in the developing pectoral fin of zebrafish. The developing pectoral fin contains an aggregation plate of differentiated chondrocytes (endochondral disc; primordium for endoskeletal components, proximal radials). The endochondral disc can be regenerated after amputation in the middle of the disc. The regenerated disc sufficiently forms endoskeletal patterns. Early in the process of regenerating the endochondral disc, epithelium with apical ectodermal ridge (AER) marker expression rapidly covers the amputation plane, and mesenchymal cells start to actively proliferate. Taken together with re-expression of a blastema marker gene, msxb, and other developmental genes, it is likely that regeneration of the endochondral disc recaptures fin development as epimorphic limb regeneration does. The ability of endoskeletal regeneration declines during larval growth, and adult zebrafish eventually lose the ability to regenerate endoskeletal components such that amputated endoskeletons become enlarged. Endoskeletal regeneration in the zebrafish pectoral fin will serve as a new model system for successful appendage regeneration in mammals.
我们首次展示了斑马鱼发育中的胸鳍内骨骼的再生。发育中的胸鳍包含一个分化的软骨细胞聚集盘(软骨内盘;内骨骼成分的原基,近端辐射)。软骨内盘在盘中部截断后可以再生。再生的软骨内盘充分形成内骨骼模式。在软骨内盘再生的早期过程中,具有顶端外胚层嵴(AER)标记物表达的上皮迅速覆盖截断平面,间质细胞开始积极增殖。与再生的软骨内盘重新表达芽基标记基因 msxb 和其他发育基因一起,很可能软骨内盘的再生重新捕获了鳍的发育,就像变态肢体再生一样。内骨骼再生的能力在幼虫生长过程中下降,成年斑马鱼最终失去了再生内骨骼成分的能力,以至于截断的内骨骼变得增大。斑马鱼胸鳍的内骨骼再生将成为哺乳动物成功的附肢再生的新模型系统。
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