Skeletal muscle inflammation and atrophy in heart failure

被引:83
作者
Lavine, Kory J. [1 ,2 ,3 ]
Sierra, Oscar L. [1 ]
机构
[1] Washington Univ, Ctr Cardiovascular Res, Sch Med St Louis, Div Cardiol, 660 S Euclid Ave,Campus Box 8086, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med St Louis, Dept Dev Biol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med St Louis, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
Macrophage; Heart failure; Skeletal muscle; Inflammation; GROWTH-FACTOR-I; NECROSIS-FACTOR-ALPHA; TISSUE-RESIDENT MACROPHAGES; HEMATOPOIETIC STEM-CELLS; LEFT-VENTRICULAR DYSFUNCTION; GENE-EXPRESSION PROFILES; MYOCARDIAL-INFARCTION; ANGIOTENSIN-II; MUSCULAR-DYSTROPHY; ALTERED INFLAMMATION;
D O I
10.1007/s10741-016-9593-0
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Heart failure represents a systemic disease with profound effects on multiple peripheral tissues including skeletal muscle. Within the context of heart failure, perturbations in skeletal muscle physiology, structure, and function strongly contribute to exercise intolerance and the morbidity of this devastating disease. There is growing evidence that chronic heart failure imparts specific pathological changes within skeletalmuscle beds resulting in muscle dysfunction and tissue atrophy. Mechanistically, systemic and local inflammatory responses drive critical aspects of this pathology. In this review, we will discuss pathological mechanisms that drive skeletal muscle inflammation and highlight emerging roles for distinct innate immune subsets that reside within damage muscle tissue focusing on the recently described embryonic and monocyte-derived macrophage lineages. Within this context, we will discuss how immune mechanisms can be differentially targeted to stimulate skeletal muscle inflammation, catabolism, fiber atrophy, and regeneration.
引用
收藏
页码:179 / 189
页数:11
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