Tazaki Akira, Tanaka Elly M, Fei Ji-Feng
Research Institute for Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus-Vienna Biocenter, 1030 Vienna, Austria.
Research Institute for Molecular Pathology (IMP), Vienna Biocenter (VBC), Campus-Vienna Biocenter, 1030 Vienna, Austria.
Dev Biol. 2017 Dec 1;432(1):63-71. doi: 10.1016/j.ydbio.2017.09.034. Epub 2017 Oct 10.
Repairing injured tissues / organs is one of the major challenges for the maintenance of proper organ function in adulthood. In mammals, the central nervous system including the spinal cord, once established during embryonic development, has very limited capacity to regenerate. In contrast, salamanders such as axolotls can fully regenerate the injured spinal cord, making this a very powerful vertebrate model system for studying this process. Here we discuss the cellular and molecular requirements for spinal cord regeneration in the axolotl. The recent development of tools to test molecular function, including CRISPR-mediated gene editing, has lead to the identification of key players involved in the cell response to injury that ultimately leads to outgrowth of neural stem cells that are competent to replay the process of spinal cord development to replace the damaged/missing tissue.
修复受损组织/器官是成年期维持器官正常功能面临的主要挑战之一。在哺乳动物中,包括脊髓在内的中枢神经系统在胚胎发育过程中一旦形成,其再生能力就非常有限。相比之下,蝾螈等蝾螈类动物能够完全再生受损的脊髓,使其成为研究这一过程的非常强大的脊椎动物模型系统。在这里,我们讨论了蝾螈脊髓再生的细胞和分子条件。包括CRISPR介导的基因编辑在内的测试分子功能工具的最新发展,已导致鉴定出参与细胞对损伤反应的关键因子,这些反应最终导致神经干细胞生长,从而能够重演脊髓发育过程以替代受损/缺失的组织。