König Désirée, Page Lionel, Chassot Bérénice, Jaźwińska Anna
Department of Biology, University of Fribourg, Chemin du Musée 10, 1700 Fribourg, Switzerland.
Department of Biology, University of Fribourg, Chemin du Musée 10, 1700 Fribourg, Switzerland.
Dev Biol. 2018 Jan 15;433(2):416-432. doi: 10.1016/j.ydbio.2017.07.024. Epub 2017 Jul 29.
The skeleton of adult zebrafish fins comprises lepidotrichia, which are dermal bones of the rays, and actinotrichia, which are non-mineralized spicules at the distal margin of the appendage. Little is known about the regenerative dynamics of the actinotrichia-specific structural proteins called Actinodins. Here, we used immunofluorescence analysis to determine the contribution of two paralogous Actinodin proteins, And1/2, in regenerating fins. Both proteins were detected in the secretory organelles in the mesenchymal cells of the blastema, but only And1 was detected in the epithelial cells of the wound epithelium. The analysis of whole mount fins throughout the entire regenerative process and longitudinal sections revealed that And1-positive fibers are complementary to the lepidotrichia. The analysis of another longfin fish, a gain-of-function mutation in the potassium channel kcnk5b, revealed that the long-fin phenotype is associated with an extended size of actinotrichia during homeostasis and regeneration. Finally, we investigated the role of several signaling pathways in actinotrichia formation and maintenance. This revealed that the pulse-inhibition of either TGFβ/Activin-βA or FGF are sufficient to impair deposition of Actinodin during regeneration. Thus, the dynamic turnover of Actinodin during fin regeneration is regulated by multiple factors, including the osteoblasts, growth rate in a potassium channel mutant, and instructive signaling networks between the epithelium and the blastema of the regenerating fin.
成年斑马鱼鳍的骨骼由鳍条(即鳍射线的真皮骨)和鳍棘(即附肢远端边缘的非矿化针状体)组成。对于名为肌动蛋白原的鳍棘特异性结构蛋白的再生动力学,我们了解甚少。在这里,我们使用免疫荧光分析来确定两种同源肌动蛋白原蛋白And1/2在鳍再生中的作用。在芽基间充质细胞的分泌细胞器中检测到了这两种蛋白,但仅在伤口上皮的上皮细胞中检测到了And1。对整个再生过程中的整装鳍和纵向切片进行分析后发现,And1阳性纤维与鳍条互补。对另一种长鳍鱼(钾通道kcnk5b功能获得性突变体)的分析表明,长鳍表型与稳态和再生过程中鳍棘尺寸的增大有关。最后,我们研究了几种信号通路在鳍棘形成和维持中的作用。结果表明,对TGFβ/激活素-βA或FGF进行脉冲抑制足以损害再生过程中肌动蛋白原的沉积。因此,鳍再生过程中肌动蛋白原的动态更新受多种因素调控,包括成骨细胞、钾通道突变体中的生长速率以及再生鳍上皮与芽基之间的指导性信号网络。