Walker S E, Yu K, Burgess S, Echeverri K
Marine Biological Laboratory, Eugene Bell Center for Regenerative Biology, Woods Hole, MA, USA.
Translational and Functional Genomics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.
NPJ Regen Med. 2025 May 8;10(1):22. doi: 10.1038/s41536-025-00413-2.
The axolotl retains a remarkable capacity for regenerative repair and is one of the few vertebrate species capable of regenerating its brain and spinal cord after injury. To date, studies investigating axolotl spinal cord regeneration have placed particular emphasis on understanding how cells immediately adjacent to the injury site respond to damage to promote regenerative repair. How neurons outside of this immediate injury site respond to an injury remains unknown. Here, we identify a population of dpErk/etv1 glutamatergic neurons in the axolotl telencephalon that are activated in response to injury and are essential for tail regeneration. Furthermore, these neurons project to the hypothalamus where they upregulate the neuropeptide neurotensin in response to injury. Together, these findings identify a unique population of neurons in the axolotl brain whose activation is necessary for successful tail regeneration, and sheds light on how neurons outside of the immediate injury site respond to an injury.
美西螈保留了显著的再生修复能力,是少数能够在受伤后再生其大脑和脊髓的脊椎动物物种之一。迄今为止,研究美西螈脊髓再生的研究特别强调了解损伤部位紧邻的细胞如何对损伤做出反应以促进再生修复。该直接损伤部位之外的神经元如何对损伤做出反应仍然未知。在这里,我们在美西螈端脑中鉴定出一群dpErk/etv1谷氨酸能神经元,它们在受到损伤时被激活,并且对尾巴再生至关重要。此外,这些神经元投射到下丘脑,在那里它们在受到损伤时会上调神经肽神经降压素。总之,这些发现确定了美西螈脑中一群独特的神经元,其激活对于成功的尾巴再生是必要的,并揭示了直接损伤部位之外的神经元如何对损伤做出反应。