4.7 Review

RAGE in the pathophysiology of skeletal muscle

期刊

JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE
卷 9, 期 7, 页码 1213-1234

出版社

WILEY
DOI: 10.1002/jcsm.12350

关键词

RAGE; AGEs; S100B; HMGB1; myogenesis; muscle wasting

资金

  1. Association Francaise contre les Myopathies [12992, 16812]
  2. Associazione Italiana per la Ricerca sul Cancro [17581]
  3. Ministero dell'Istruzione, dell'Universita e della Ricerca, Italy [PRIN 2009WBFZYM_002, PRIN 2010R8JK2X_004, PRIN 2012N8YJC3]
  4. Fondazione Cassa di Risparmio di Perugia [2012.0241.021, 2015.0325.021, 2016-0136.021]

向作者/读者索取更多资源

Emerging evidence suggests that the signalling of the Receptor for Advanced Glycation End products (RAGE) is critical for skeletal muscle physiology controlling both the activity of muscle precursors during skeletal muscle development and the correct time of muscle regeneration after acute injury. On the other hand, the aberrant re-expression/activity of RAGE in adult skeletal muscle is a hallmark of muscle wasting that occurs in response to ageing, genetic disorders, inflammatory conditions, cancer, and metabolic alterations. In this review, we discuss the mechanisms of action and the ligands of RAGE involved in myoblast differentiation, muscle regeneration, and muscle pathological conditions. We highlight potential therapeutic strategies for targeting RAGE to improve skeletal muscle function.

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