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      Laminin mimetic peptide nanofibers regenerate acute muscle defect

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      Author(s)
      Cimenci, C. E.
      Uzunalli, G.
      Uysal, O.
      Yergoz, F.
      Umay, E. K.
      Güler, Mustafa O.
      Tekinay, A. B.
      Date
      2017
      Source Title
      Acta Biomaterialia
      Print ISSN
      1742-7061
      Electronic ISSN
      1878-7568
      Publisher
      Acta Materialia Inc
      Volume
      60
      Pages
      190 - 200
      Language
      English
      Type
      Article
      Item Usage Stats
      218
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      418
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      Abstract
      Skeletal muscle cells are terminally differentiated and require the activation of muscle progenitor (satellite) cells for their regeneration. There is a clinical need for faster and more efficient treatment methods for acute muscle injuries, and the stimulation of satellite cell proliferation is promising in this context. In this study, we designed and synthesized a laminin-mimetic bioactive peptide (LM/E-PA) system that is capable of accelerating satellite cell activation by emulating the structure and function of laminin, a major protein of the basal membrane of the skeletal muscle. The LM/E-PA nanofibers enhance myogenic differentiation in vitro and the clinical relevance of the laminin-mimetic bioactive scaffold system was demonstrated further by assessing its effect on the regeneration of acute muscle injury in a rat model. Laminin mimetic peptide nanofibers significantly promoted satellite cell activation in skeletal muscle and accelerated myofibrillar regeneration following acute muscle injury. In addition, the LM/E-PA scaffold treatment significantly reduced the time required for the structural and functional repair of skeletal muscle. This study represents one of the first examples of molecular- and tissue-level regeneration of skeletal muscle facilitated by bioactive peptide nanofibers following acute muscle injury. Significance Statement Sports, heavy lifting and other strength-intensive tasks are ubiquitous in modern life and likely to cause acute skeletal muscle injury. Speeding up regeneration of skeletal muscle injuries would not only shorten the duration of recovery for the patient, but also support the general health and functionality of the repaired muscle tissue. In this work, we designed and synthesized a laminin-mimetic nanosystem to enhance muscle regeneration. We tested its activity in a rat tibialis anterior muscle by injecting the bioactive nanosystem. The evaluation of the regeneration and differentiation capacity of skeletal muscle suggested that the laminin-mimetic nanosystem enhances skeletal muscle regeneration and provides a suitable platform that is highly promising for the regeneration of acute muscle injuries. This work demonstrates for the first time that laminin-mimetic self-assembled peptide nanosystems facilitate myogenic differentiation in vivo without the need for additional treatment.
      Keywords
      Acute muscle injury
      Functional self-assembly
      Hydrogel
      Laminin
      Peptide nanofiber
      Regeneration
      Cardiotoxin
      Laminin
      MyoD1 protein
      Myogenin
      Nanofiber
      Peptide
      Transcription factor PAX7
      Animal behavior
      Animal experiment
      Animal model
      Animal tissue
      Article
      Basal lamina
      Cell activation
      Cell differentiation
      Circular dichroism
      Comparative study
      Controlled study
      Flow kinetics
      High performance liquid chromatography
      Hydrogel
      In vitro study
      In vivo study
      Liquid chromatography-mass spectrometry
      Male
      Muscle cell
      Muscle development
      Muscle disease
      Muscle regeneration
      Nonhuman
      pH
      Priority journal
      Protein analysis
      Protein expression
      Protein function
      Protein structure
      Rat
      Reverse transcription polymerase chain reaction
      Satellite cell
      Scanning electron microscopy
      Synthesis
      Transmission electron microscopy
      Western blotting
      Permalink
      http://hdl.handle.net/11693/37442
      Published Version (Please cite this version)
      http://dx.doi.org/10.1016/j.actbio.2017.07.010
      Collections
      • Institute of Materials Science and Nanotechnology (UNAM) 2258
      • Nanotechnology Research Center (NANOTAM) 1179
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