Department of Neuroscience, Washington University School of Medicine, St Louis, MO, 63110, USA.
Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO, 63110, USA.
Nat Commun. 2020 Sep 29;11(1):4891. doi: 10.1038/s41467-020-18642-y.
Peripheral sensory neurons regenerate their axon after nerve injury to enable functional recovery. Intrinsic mechanisms operating in sensory neurons are known to regulate nerve repair, but whether satellite glial cells (SGC), which completely envelop the neuronal soma, contribute to nerve regeneration remains unexplored. Using a single cell RNAseq approach, we reveal that SGC are distinct from Schwann cells and share similarities with astrocytes. Nerve injury elicits changes in the expression of genes related to fatty acid synthesis and peroxisome proliferator-activated receptor (PPARα) signaling. Conditional deletion of fatty acid synthase (Fasn) in SGC impairs axon regeneration. The PPARα agonist fenofibrate rescues the impaired axon regeneration in mice lacking Fasn in SGC. These results indicate that PPARα activity downstream of FASN in SGC contributes to promote axon regeneration in adult peripheral nerves and highlight that the sensory neuron and its surrounding glial coat form a functional unit that orchestrates nerve repair.
外周感觉神经元在神经损伤后会再生其轴突,从而实现功能恢复。已知感觉神经元中的内在机制可调节神经修复,但完全包裹神经元胞体的卫星胶质细胞 (SGC) 是否有助于神经再生仍未被探索。我们使用单细胞 RNAseq 方法揭示了 SGC 与施万细胞不同,但与星形胶质细胞具有相似之处。神经损伤会引起与脂肪酸合成和过氧化物酶体增殖物激活受体 (PPARα) 信号相关的基因表达发生变化。SGC 中脂肪酸合酶 (Fasn) 的条件性缺失会损害轴突再生。PPARα 激动剂非诺贝特可挽救 SGC 中 Fasn 缺失小鼠的受损轴突再生。这些结果表明,SGC 中 FASN 下游的 PPARα 活性有助于促进成年周围神经中的轴突再生,并强调感觉神经元及其周围的神经胶质鞘形成了一个协调神经修复的功能单元。