Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-Innovation Center of Neuroregeneration, NMPA Key Laboratory for Research and Evaluation of Tissue Engineering Technology Products, Nantong University, Nantong, Jiangsu, China.
Mol Neurobiol. 2023 Jan;60(1):329-341. doi: 10.1007/s12035-022-03090-0. Epub 2022 Oct 20.
Transcription factors are master regulators of various cellular processes under diverse physiological and pathological conditions. Many transcription factors that are differentially expressed after injury to peripheral nerves play important roles in nerve regeneration. Considering that rapid and timely regrowth of injured axons is a prerequisite for successful target reinnervation, here, we compile transcription factors that mediates axon elongation, including axon growth suppressor Klf4 and axon growth promoters c-Myc, Sox11, STAT3, Atf3, c-Jun, Smad1, C/EBPδ, and p53. Besides neuronal changes, Schwann cell phenotype modulation is also critical for nerve regeneration. The activation of Schwann cells at early time points post injury provides a permissive microenvironment whereas the re-differentiation of Schwann cells at later time points supports myelin sheath formation. Hence, c-Jun and Sox2, two critical drivers for Schwann cell reprogramming, as well as Krox-20 and Sox10, two essential regulators of Schwann cell myelination, are reviewed. These transcription factors may serve as promising targets for promoting the functional recovery of injured peripheral nerves.
转录因子是各种生理和病理条件下细胞过程的主要调节因子。在外周神经损伤后差异表达的许多转录因子在神经再生中发挥重要作用。考虑到受伤轴突的快速和及时再生是成功靶神经再支配的前提,在这里,我们编译了介导轴突伸长的转录因子,包括轴突生长抑制因子 Klf4 和轴突生长促进因子 c-Myc、Sox11、STAT3、Atf3、c-Jun、Smad1、C/EBPδ 和 p53。除了神经元变化,施万细胞表型的调节对于神经再生也是至关重要的。损伤后早期施万细胞的激活提供了一个允许的微环境,而晚期施万细胞的再分化则支持髓鞘形成。因此,c-Jun 和 Sox2,这两个施万细胞重编程的关键驱动因子,以及 Krox-20 和 Sox10,这两个施万细胞髓鞘形成的必需调节因子,都进行了综述。这些转录因子可能成为促进损伤外周神经功能恢复的有希望的靶点。