Scimone M Lucila, Canales Bryanna Isela-Inez, Aoude Patrick, Atabay Kutay D, Reddien Peter W
Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts, United States of America.
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts, United States of America.
PLoS Genet. 2025 Jan 27;21(1):e1011577. doi: 10.1371/journal.pgen.1011577. eCollection 2025 Jan.
Some animals can regenerate large missing regions of their nervous system, requiring mechanisms to restore the pattern, numbers, and wiring of diverse neuron classes. Because injuries are unpredictable, regeneration must be accomplished from an unlimited number of starting points. Coordinated regeneration of neuron-glia architecture is thus a major challenge and remains poorly understood. In planarians, neurons and glia are regenerated from distinct progenitors. We found that planarians first regenerate neurons expressing a Delta-encoding gene, delta-2, at key positions in the central and peripheral nervous systems. Planarian glia are specified later from dispersed Notch-1-expressing mesoderm-like phagocytic progenitors. Inhibition of delta-2 or notch-1 severely reduced glia in planarians, but did not affect the specification of other phagocytic cell types. Loss of several delta-2-expressing neuron classes prevented differentiation of the glia associated with them, whereas transplantation of delta-2-expressing photoreceptor neurons was sufficient for glia formation at an ectopic location. Our results suggest a model in which patterned delta-2-expressing neurons instruct phagocytic progenitors to locally differentiate into glia, presenting a mechanism for coordinated regeneration of numbers and pattern of cell types.
一些动物能够再生其神经系统中大片缺失的区域,这需要多种机制来恢复不同神经元类别的模式、数量和连接方式。由于损伤是不可预测的,再生必须从无数个起始点开始。因此,神经胶质细胞结构的协调再生是一项重大挑战,目前仍知之甚少。在涡虫中,神经元和神经胶质细胞由不同的祖细胞再生而来。我们发现,涡虫首先在中枢神经系统和外周神经系统的关键位置再生出表达编码Delta的基因delta-2的神经元。涡虫的神经胶质细胞稍后由分散的表达Notch-1的中胚层样吞噬祖细胞分化而来。抑制delta-2或Notch-1会严重减少涡虫中的神经胶质细胞,但不影响其他吞噬细胞类型的分化。几种表达delta-2的神经元类别的缺失会阻止与之相关的神经胶质细胞的分化,而移植表达delta-2的感光神经元足以在异位位置形成神经胶质细胞。我们的研究结果提出了一个模型,即表达delta-2的模式化神经元指导吞噬祖细胞在局部分化为神经胶质细胞,这为细胞类型数量和模式的协调再生提供了一种机制。