Girgenrath Mahasweta, Weng Shawn, Kostek Christine A, Browning Beth, Wang Monica, Brown Sharron A N, Winkles Jeffrey A, Michaelson Jennifer S, Allaire Norm, Schneider Pascal, Scott Martin L, Hsu Yen-ming, Yagita Hideo, Flavell Richard A, Miller Jeffrey Boone, Burkly Linda C, Zheng Timothy S
Boston Biomedical Research Institute, Watertown, MA, USA.
EMBO J. 2006 Dec 13;25(24):5826-39. doi: 10.1038/sj.emboj.7601441. Epub 2006 Nov 23.
Inflammation participates in tissue repair through multiple mechanisms including directly regulating the cell fate of resident progenitor cells critical for successful regeneration. Upon surveying target cell types of the TNF ligand TWEAK, we observed that TWEAK binds to all progenitor cells of the mesenchymal lineage and induces NF-kappaB activation and the expression of pro-survival, pro-proliferative and homing receptor genes in the mesenchymal stem cells, suggesting that this pro-inflammatory cytokine may play an important role in controlling progenitor cell biology. We explored this potential using both the established C2C12 cell line and primary mouse muscle myoblasts, and demonstrated that TWEAK promoted their proliferation and inhibited their terminal differentiation. By generating mice deficient in the TWEAK receptor Fn14, we further showed that Fn14-deficient primary myoblasts displayed significantly reduced proliferative capacity and altered myotube formation. Following cardiotoxin injection, a known trigger for satellite cell-driven skeletal muscle regeneration, Fn14-deficient mice exhibited reduced inflammatory response and delayed muscle fiber regeneration compared with wild-type mice. These results indicate that the TWEAK/Fn14 pathway is a novel regulator of skeletal muscle precursor cells and illustrate an important mechanism by which inflammatory cytokines influence tissue regeneration and repair. Coupled with our recent demonstration that TWEAK potentiates liver progenitor cell proliferation, the expression of Fn14 on all mesenchymal lineage progenitor cells supports a broad involvement of this pathway in other tissue injury and disease settings.
炎症通过多种机制参与组织修复,包括直接调节对成功再生至关重要的驻留祖细胞的细胞命运。在研究肿瘤坏死因子配体TWEAK的靶细胞类型时,我们观察到TWEAK与间充质谱系的所有祖细胞结合,并诱导间充质干细胞中核因子κB的激活以及促存活、促增殖和归巢受体基因的表达,这表明这种促炎细胞因子可能在控制祖细胞生物学方面发挥重要作用。我们使用已建立的C2C12细胞系和原代小鼠肌肉成肌细胞探索了这种潜力,并证明TWEAK促进了它们的增殖并抑制了它们的终末分化。通过生成TWEAK受体Fn14缺陷的小鼠,我们进一步表明Fn14缺陷的原代成肌细胞增殖能力显著降低,肌管形成改变。在注射已知的卫星细胞驱动的骨骼肌再生触发因子心肌毒素后,与野生型小鼠相比,Fn14缺陷小鼠的炎症反应减弱,肌肉纤维再生延迟。这些结果表明TWEAK/Fn14途径是骨骼肌前体细胞的一种新型调节因子,并阐明了炎症细胞因子影响组织再生和修复的重要机制。结合我们最近证明TWEAK增强肝祖细胞增殖,Fn14在所有间充质谱系祖细胞上的表达支持该途径在其他组织损伤和疾病环境中的广泛参与。