Pegoretti Valentina, Boerema Ate, Kats Kim, Dafauce Garcia Juan M, Fischer Roman, Kontermann Roland E, Pfizenmaier Klaus, Laman Jon D, Eisel Ulrich L M, Baron Wia
Department of Molecular Neurobiology, Groningen, Institute of Evolutionary Life Science (GELIFES), University of Groningen, Groningen, The Netherlands.
Department Biomedical Sciences, Section Molecular Cell Biology, University of Groningen, University Medical Center Groningen (UMCG), Groningen, The Netherlands.
J Mol Med (Berl). 2025 May 10. doi: 10.1007/s00109-025-02549-6.
The development of therapeutics that enhances the regeneration of myelin sheaths following demyelination is predicted to prevent neurodegeneration. A promising target to enhance remyelination is the immunomodulatory cytokine tumor necrosis factor alpha (TNFα) and its receptors TNFR1 and TNFR2. TNFR2 on oligodendrocyte lineage cells and microglia coordinates different protective functions, such as proliferation of oligodendrocyte progenitor cells, survival of mature oligodendrocytes, and release of anti-inflammatory cytokines, in animal models of inflammation and demyelination. Here, we find in the cuprizone model that following demyelination, fewer axons are unmyelinated in the corpus callosum at an early stage of remyelination after single TNFR2 agonist delivery in the lateral ventricle, while astrocyte and microglia number and coverage are unchanged. Towards later stages of remyelination, TNFR2 agonist treatment maintains the number of oligodendrocyte lineage cells, and large caliber axons have thinner myelin. Hence, even short-term stimulation of TNFR2 has a positive impact on the remyelination processes. This study informs further on the beneficial implications of TNFR2 signaling on oligodendrocyte lineage cells and remyelination, emphasizing its potential therapeutic value for demyelinating diseases, including multiple sclerosis. KEY MESSAGES: Single TNFR2 agonist treatment in the lateral ventricle following cuprizone-induced demyelination impacts remyelination by: Leading to a lower percentage of unmyelinated axons at early stages. Preserving the number of oligodendrocyte lineage cells in the corpus callosum at later stages. Covering large calibre axons with thinner myelin sheaths at later stages.
预计开发出能促进脱髓鞘后髓鞘再生的疗法可预防神经退行性变。免疫调节细胞因子肿瘤坏死因子α(TNFα)及其受体TNFR1和TNFR2是促进髓鞘再生的一个有前景的靶点。在炎症和脱髓鞘动物模型中,少突胶质细胞谱系细胞和小胶质细胞上的TNFR2可协调不同的保护功能,如少突胶质前体细胞的增殖、成熟少突胶质细胞的存活以及抗炎细胞因子的释放。在此,我们在铜螯合剂模型中发现,脱髓鞘后,在侧脑室单次递送TNFR2激动剂后,在髓鞘再生早期胼胝体中未髓鞘化的轴突较少,而星形胶质细胞和小胶质细胞的数量及覆盖范围未改变。在髓鞘再生后期,TNFR2激动剂治疗可维持少突胶质细胞谱系细胞的数量,且大口径轴突的髓鞘较薄。因此,即使是对TNFR2的短期刺激也对髓鞘再生过程有积极影响。本研究进一步说明了TNFR2信号传导对少突胶质细胞谱系细胞和髓鞘再生的有益影响,强调了其对包括多发性硬化症在内的脱髓鞘疾病的潜在治疗价值。关键信息:在铜螯合剂诱导的脱髓鞘后,侧脑室单次注射TNFR2激动剂对髓鞘再生的影响如下:在早期导致未髓鞘化轴突的比例降低。在后期保留胼胝体中少突胶质细胞谱系细胞的数量。在后期用较薄的髓鞘覆盖大口径轴突。