State Key Laboratory of Stem Cell and Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China.
Department of Orthopaedic Surgery, Affiliated Hospital of Guilin Medical University, Guilin, Guangxi, 541001, China.
Cell Death Differ. 2018 Sep;25(9):1598-1611. doi: 10.1038/s41418-018-0064-0. Epub 2018 Feb 19.
Neurons in the central nervous system (CNS) lose their intrinsic ability and fail to regenerate, but the underlying mechanisms are largely unknown. Polycomb group (PcG) proteins, which include PRC1 and PRC2 complexes function as gene repressors and are involved in many biological processes. Here we report that PRC1 components (polycomb chromobox (CBX) 2, 7, and 8) are novel regulators of axon growth and regeneration. Especially, knockdown of CBX7 in either embryonic cortical neurons or adult dorsal root ganglion (DRG) neurons enhances their axon growth ability. Two important transcription factors GATA4 and SOX11 are functional downstream targets of CBX7 in controlling axon regeneration. Moreover, knockdown of GATA4 or SOX11 in cultured DRG neurons inhibits axon regeneration response from CBX7 downregulation in DRG neurons. These findings suggest that targeting CBX signaling pathway may be a novel approach for promoting the intrinsic regenerative capacity of damaged CNS neurons.
中枢神经系统(CNS)中的神经元丧失了内在能力,无法再生,但潜在的机制在很大程度上尚不清楚。多梳组(PcG)蛋白,包括 PRC1 和 PRC2 复合物,作为基因抑制剂发挥作用,参与许多生物过程。在这里,我们报告 PRC1 成分(多梳盒(CBX)2、7 和 8)是轴突生长和再生的新型调节剂。特别是,在胚胎皮质神经元或成年背根神经节(DRG)神经元中敲低 CBX7 可增强其轴突生长能力。两个重要的转录因子 GATA4 和 SOX11 是 CBX7 控制轴突再生的功能下游靶标。此外,在培养的 DRG 神经元中敲低 GATA4 或 SOX11 会抑制从 DRG 神经元中 CBX7 下调引起的轴突再生反应。这些发现表明,靶向 CBX 信号通路可能是促进受损 CNS 神经元内在再生能力的一种新方法。