HMGB1 expression and muscle regeneration in idiopathic inflammatory myopathies and degenerative joint diseases

被引:14
作者
Cseri, Karolina [1 ]
Vincze, Janos [2 ]
Cseri, Julianna [3 ]
Fodor, Janos [2 ]
Csernatony, Zoltan [4 ]
Csernoch, Laszlo [2 ]
Danko, Katalin [1 ]
机构
[1] Univ Debrecen, Div Clin Immunol, Inst Med, Ctr Clin, H-4012 Debrecen, Hungary
[2] Univ Debrecen, Fac Med, Dept Physiol, H-4012 Debrecen, Hungary
[3] Univ Debrecen, Dept Physiotherapy, Fac Publ Hlth, H-4012 Debrecen, Hungary
[4] Univ Debrecen, Dept Orthopaed Surg, Ctr Clin, H-4012 Debrecen, Hungary
关键词
HMGB1; Differentiation; Idiopathic inflammatory myopathy; Myogenesis; Muscle regeneration; Proliferation; Skeletal muscle; GROUP BOX PROTEIN-1; MOBILITY; CYTOKINE; RECEPTOR; HMG-1;
D O I
10.1007/s10974-015-9411-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The High-Mobility Group Box 1 protein (HMGB1) is a known nuclear protein which may be released from the nucleus into the cytoplasm and the extracellular space. It is believed that the mobilized HMGB1 plays role in the autoimmune processes as an alarmin, stimulating the immune response. In addition, muscle regeneration and differentiation may also be altered in the inflammatory surroundings. Biopsy specimens derived from patients with idiopathic inflammatory myopathies (IIM) such as polymyositis or dermatomyositis were compared to muscle samples from patients undergoing surgical interventions for coxarthrosis. The biopsy and surgery specimens were used for Western blot analysis, for immunohistochemical detection of HMGB1 in histological preparations and for cell culturing to examine cell proliferation and differentiation. Our data show lower HMGB1 expression, impaired proliferation and slightly altered fusion capacity in the primary cell cultures started from IIM specimens than in cultures of coxarthrotic muscles. The ratio of regenerating muscle fibres with centralised nuclei (myotubes) is lower in the IIM samples than in the coxarthrotic ones but corticosteroid treatment shifts the ratio towards the coxarthrotic value. Our data suggest that the impaired regeneration capacity should also be considered to be behind the muscle weakness in IIM patients. The role of HMGB1 as a pathogenic signal requires further investigation.
引用
收藏
页码:255 / 262
页数:8
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