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Repairing Volumetric Muscle Loss in the Ovine Peroneus Tertius Following a 3-Month Recovery.
Novakova, Stoyna S; Rodriguez, Brittany L; Vega-Soto, Emmanuel E; Nutter, Genevieve P; Armstrong, Rachel E; Macpherson, Peter C D; Larkin, Lisa M.
Afiliação
  • Novakova SS; Department of Molecular and Integrative Physiology and University of Michigan, Ann Arbor, Michigan, USA.
  • Rodriguez BL; Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan, USA.
  • Vega-Soto EE; Department of Molecular and Integrative Physiology and University of Michigan, Ann Arbor, Michigan, USA.
  • Nutter GP; Department of Molecular and Integrative Physiology and University of Michigan, Ann Arbor, Michigan, USA.
  • Armstrong RE; Department of Molecular and Integrative Physiology and University of Michigan, Ann Arbor, Michigan, USA.
  • Macpherson PCD; Department of Molecular and Integrative Physiology and University of Michigan, Ann Arbor, Michigan, USA.
  • Larkin LM; Department of Molecular and Integrative Physiology and University of Michigan, Ann Arbor, Michigan, USA.
Tissue Eng Part A ; 26(15-16): 837-851, 2020 08.
Article em En | MEDLINE | ID: mdl-32013753
Much effort has been made to fabricate engineered tissues on a scale that is clinically relevant to humans; however, scale-up remains one of the most significant technological challenges of tissue engineering to date. To address this limitation, our laboratory has developed tissue-engineered skeletal muscle units (SMUs) and engineered neural conduits (ENCs), and modularly scaled them to clinically relevant sizes for the treatment of volumetric muscle loss (VML). The goal of this study was to evaluate the SMUs and ENCs in vitro, and to test the efficacy of our SMUs and ENCs in restoring muscle function in a clinically relevant large animal (sheep) model. The animals received a 30% VML injury to the peroneus tertius muscle and were allowed to recover for 3 months. The animals were divided into three experimental groups: VML injury without a repair (VML only), repair with an SMU (VML+SMU), or repair with an SMU and ENC (VML+SMU+ENC). We evaluated the SMUs before implantation and found that our single scaled-up SMUs were characterized by the presence of contracting myotubes, linearly aligned extracellular matrix proteins, and Pax7+ satellite cells. Three months after implantation, we found that the repair groups (VML+SMU and VML+SMU+ENC) had restored muscle mass and tetanic force production to a level that was statistically indistinguishable from the uninjured contralateral muscle after 3 months in vivo. Furthermore, we demonstrated the ability of our ENCs to effectively bridge the gap between native nerve and the repair site by eliciting a muscle contraction through direct electrical stimulation of the re-routed nerve. Impact statement The fabrication of tissues of clinically relevant sizes is one of the largest obstacles preventing engineered tissues from achieving widespread use in the clinic. This study aimed to combat this limitation by developing a fabrication method to scale-up tissue-engineered skeletal muscle for the treatment of volumetric muscle loss in a large animal (sheep) model and evaluating the efficacy of the tissue-engineered constructs after a 3-month recovery.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Engenharia Tecidual / Doenças Musculares Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Músculo Esquelético / Engenharia Tecidual / Doenças Musculares Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article