Role of TNF- signaling in regeneration of cardiotoxin-injured muscle

Chen, Shuen-Ei, Eric Gerken, Yingmin Zhang, Mei Zhan, Raja K. Mohan, Andrew S. Li, Michael B. Reid, and Yi-Ping Li. Role of TNFsignaling in regeneration of cardiotoxin-injured muscle. Am J Physiol Cell Physiol 289: C1179–C1187, 2005. First published August 3, 2005; doi:10.1152/ajpcell.00062.2005.—Recent data suggest a physiological role for the proinflammatory cytokine TNFin skeletal muscle regeneration. However, the underlying mechanism is not understood. In the present study, we analyzed TNF-activated signaling pathways involved in myogenesis in soleus muscle injured by cardiotoxin (CTX) in TNFreceptor double-knockout mice (p55 / p75 / ). We found that activation of p38MAPK, which is critical for myogenesis, was blocked in CTX-injured p55 / p75 / soleus on day 3 postinjury when myogenic differentiation was being initiated, while activation of ERK1/2 and JNK MAPK, as well as transcription factor NFB, was not reduced. Consequently, the phosphorylation of transcription factor myocyte enhancer factor-2C, which is catalyzed by p38 and crucial for the expression of muscle-specific genes, was blunted. Meanwhile, expression of p38-dependent differentiation marker myogenin and p21 were suppressed. In addition, expression of cyclin D1 was fivefold that in wild-type (WT) soleus. These results suggest that myogenic differentiation is blocked or delayed in the absence of TNFsignaling. Histological studies revealed abnormalities in regenerating p55 / p75 / soleus. On day 5 postinjury, new myofiber formation was clearly observed in WT soleus but not in p55 / p75 / soleus. To the contrary, p55 / p75 / soleus displayed renewed inflammation and dystrophic calcification. On day 12 postinjury, the muscle architecture of WT soleus was largely restored. Yet, in p55 / p75 / soleus, multifocal areas of inflammation, myofiber death, and myofibers with smaller cross-sectional area were observed. Functional studies demonstrated an attenuated recovery of contractile force in injured p55 / p75 / soleus. These data suggest that TNFsignaling plays a critical regulatory role in muscle regeneration.