Cellular and Molecular Mechanisms of Zebrafish Fin Regeneration

• Main Author: McMillan, Stephanie
• Other Authors: Akimenko, Marie-Andrée
• Language: en
• Published: Université d'Ottawa / University of Ottawa 2016
• Subjects: Zebrafish; Caudal Fin; Pectoral Fin; Regeneration
• Online Access: http://hdl.handle.net/10393/35241; http://dx.doi.org/10.20381/ruor-199

During fin regeneration, a blastema, a group of de-differentiated cells, forms underneath the wound epidermis. As regeneration proceeds, cells leave the proximal blastema and enter the differentiation zone. Adjacent to the differentiation zone, a subset of cells in the basal epidermal layer (BEL) express sonic hedgehog a (shha). Cells that come in contact with BEL differentiate into osteoblasts and joint cells, enabling the formation of bone segments at the end of each fin ray. Generally, fin regeneration occurs similarly in males and females. However, breeding tubercles (BT), keratinized epidermal structures on the male pectoral fin, result in regenerative differences when compared to females. In this thesis, three aspects of zebrafish fin regeneration were studied: 1) Cell lineage tracing of shha-expressing cells in the caudal fin regenerate; 2) The differentiation of joint cells and osteoblasts in the caudal fin regenerate; 3) Regeneration of pectoral fin BTs. Studies on caudal fin regenerates suggest osteoblasts and joint cells originate from a common cell lineage, but are committed to different cell fates. Joint cells follow a genetic pathway in which evx1 occurs downstream or parallel to hoxa13a and upstream of pthrp1. In the absence of Evx1, presumptive joint cells are committed to an osteoblast cell fate. Furthermore, joint cells do not regenerate following laser cell ablation, suggesting joint cell differentiation occurs only at specific intervals during osteoblast regeneration. Collectively, these results suggest a mechanism for joint cell differentiation during caudal fin regeneration. Studies on pectoral fins indicate androgens induce and estrogens inhibit BT formation. BT regeneration in males and androgen-treated females follows the initiation of revascularization, but occurs concomitantly with a novel second wave of angiogenesis. The inhibition of angiogenesis in androgen-treated females prevents BT formation. Altogether, these results suggest the growth and regeneration of BTs requires a v hormonal stimulus and the presence of an additional blood vessel network naturally found in males. In conclusion, these studies have increased the overall knowledge of key aspects of zebrafish fin regeneration. A gain in understanding zebrafish regeneration provides a basis in which treatments can be developed to induce regeneration in species with limited regenerative capabilities.