From Innate to Adaptive Immune Response in Muscular Dystrophies and Skeletal Muscle Regeneration: The Role of Lymphocytes

被引:44
作者
Madaro, Luca [1 ]
Bouche, Marina [2 ]
机构
[1] IRCCS Fdn Santa Lucia, I-00143 Rome, Italy
[2] Univ Roma La Sapienza, Unit Histol & Med Embryol, DAHFMO, I-00161 Rome, Italy
关键词
KINASE-C-THETA; REGULATORY T-CELLS; SATELLITE CELL; FIBRO/ADIPOGENIC PROGENITORS; PROMOTES FIBROSIS; MYOSITIS MUSCLE; NULL MUTATION; MAST-CELLS; INFLAMMATION; MOUSE;
D O I
10.1155/2014/438675
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Skeletal muscle is able to restore contractile functionality after injury thanks to its ability to regenerate. Following muscle necrosis, debris is removed by macrophages, and muscle satellite cells (MuSCs), the muscle stem cells, are activated and subsequently proliferate, migrate, and form muscle fibers restoring muscle functionality. In most muscle dystrophies (MDs), MuSCs fail to properly proliferate, differentiate, or replenish the stem cell compartment, leading to fibrotic deposition. However, besides MuSCs, interstitial nonmyogenic cells and inflammatory cells also play a key role in orchestrating muscle repair. A complete understanding of the complexity of these mechanisms should allow the design of interventions to attenuate MDs pathology without disrupting regenerative processes. In this review we will focus on the contribution of immune cells in the onset and progression of MDs, with particular emphasis on Duchenne muscular dystrophy (DMD). We will briefly summarize the current knowledge and recent advances made in our understanding of the involvement of different innate immune cells in MDs and will move on to critically evaluate the possible role of cell populations within the acquired immune response. Revisiting previous observations in the light of recent evidence will likely change our current view of the onset and progression of the disease.
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