4.7 Review

Striated muscle function, regeneration, and repair

期刊

CELLULAR AND MOLECULAR LIFE SCIENCES
卷 73, 期 22, 页码 4175-4202

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00018-016-2285-z

关键词

Muscle; Cardiac; Skeletal; Tissue engineering; Stem cells; iPS

资金

  1. NIH Grants from National Institute of Arthritis and Musculoskeletal and Skin Disease [AR055226, AR065873]
  2. NIH Grants from National Heart, Lung, and Blood Institute [HL104326, HL122079]
  3. NIH Grant Medical Scientist Training Program [T32 GM007171]
  4. NIH Common Fund for the Micro-physiological Systems Initiative [UH3TR000505]
  5. Fondation Leducq

向作者/读者索取更多资源

As the only striated muscle tissues in the body, skeletal and cardiac muscle share numerous structural and functional characteristics, while exhibiting vastly different size and regenerative potential. Healthy skeletal muscle harbors a robust regenerative response that becomes inadequate after large muscle loss or in degenerative pathologies and aging. In contrast, the mammalian heart loses its regenerative capacity shortly after birth, leaving it susceptible to permanent damage by acute injury or chronic disease. In this review, we compare and contrast the physiology and regenerative potential of native skeletal and cardiac muscles, mechanisms underlying striated muscle dysfunction, and bioengineering strategies to treat muscle disorders. We focus on different sources for cellular therapy, biomaterials to augment the endogenous regenerative response, and progress in engineering and application of mature striated muscle tissues in vitro and in vivo. Finally, we discuss the challenges and perspectives in translating muscle bioengineering strategies to clinical practice.

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