Lehrberg Jeffrey, Gardiner David M
Department of Developmental and Cell Biology, University of California Irvine, Irvine, California, United States of America.
PLoS One. 2015 Apr 29;10(4):e0123186. doi: 10.1371/journal.pone.0123186. eCollection 2015.
We have modified and optimized the technique of organotypic slice culture in order to study the mechanisms regulating growth and pattern formation in regenerating axolotl limb blastemas. Blastema cells maintain many of the behaviors that are characteristic of blastemas in vivo when cultured as slices in vitro, including rates of proliferation that are comparable to what has been reported in vivo. Because the blastema slices can be cultured in basal medium without fetal bovine serum, it was possible to test the response of blastema cells to signaling molecules present in serum, as well as those produced by nerves. We also were able to investigate the response of blastema cells to experimentally regulated changes in BMP signaling. Blastema cells responded to all of these signals by increasing the rate of proliferation and the level of expression of the blastema marker gene, Prrx-1. The organotypic slice culture model provides the opportunity to identify and characterize the spatial and temporal co-regulation of pathways in order to induce and enhance a regenerative response.
我们对器官型切片培养技术进行了改进和优化,以便研究调控再生蝾螈肢体芽基生长和模式形成的机制。当作为切片在体外培养时,芽基细胞保持了许多在体内芽基所特有的行为,包括与体内报道相当的增殖速率。由于芽基切片可以在不含胎牛血清的基础培养基中培养,因此有可能测试芽基细胞对血清中存在的信号分子以及神经产生的信号分子的反应。我们还能够研究芽基细胞对BMP信号通路实验性调控变化的反应。芽基细胞通过增加增殖速率和芽基标记基因Prrx-1的表达水平来响应所有这些信号。器官型切片培养模型为识别和表征通路的时空协同调控提供了机会,以诱导和增强再生反应。