Department of Neurology, Northwestern Feinberg School of Medicine, Chicago, IL, USA.
Department of Neurology, Brigham and Women's Hospital and Harvard Medical School, 60 Fenwood Road, Boston, MA 02115, USA.
Cell Rep. 2022 Jul 19;40(3):111130. doi: 10.1016/j.celrep.2022.111130.
Peripheral nervous system (PNS) injuries initiate transcriptional changes in glial cells and sensory neurons that promote axonal regeneration. While the factors that initiate the transcriptional changes in glial cells are well characterized, the full range of stimuli that initiate the response of sensory neurons remain elusive. Here, using a genetic model of glial cell ablation, we find that glial cell loss results in transient PNS demyelination without overt axonal loss. By profiling sensory ganglia at single-cell resolution, we show that glial cell loss induces a transcriptional injury response preferentially in proprioceptive and Aβ RA-LTMR neurons. The transcriptional response of sensory neurons to mechanical injury has been assumed to be a cell-autonomous response. By identifying a similar response in non-injured, demyelinated neurons, our study suggests that this represents a non-cell-autonomous transcriptional response of sensory neurons to glial cell loss and demyelination.
周围神经系统(PNS)损伤会引发神经胶质细胞和感觉神经元的转录变化,从而促进轴突再生。虽然已经很好地描述了引发神经胶质细胞转录变化的因素,但引发感觉神经元反应的全部刺激仍然难以捉摸。在这里,我们使用胶质细胞消融的遗传模型,发现神经胶质细胞的丢失会导致短暂的周围神经脱髓鞘,而没有明显的轴突丢失。通过单细胞分辨率对感觉神经节进行分析,我们发现神经胶质细胞的丢失会优先诱导本体感受和 Aβ RA-LTMR 神经元的转录损伤反应。人们一直认为感觉神经元对机械损伤的转录反应是一种细胞自主反应。通过在未受伤的脱髓鞘神经元中鉴定出类似的反应,我们的研究表明,这代表了感觉神经元对神经胶质细胞丢失和脱髓鞘的非细胞自主转录反应。