Perfusion-decellularized skeletal muscle as a three-dimensional scaffold with a vascular network template

Jian Zhang, Zhi Qian Hu, Neill J. Turner, Shi Feng Teng, Wen Yue Cheng, Hai Yang Zhou, Li Zhang, Hong Wei Hu, Qiang Wang*, Stephen F. Badylak

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

113 Scopus citations

Abstract

There exists a great need for repair grafts with similar volume to human skeletal muscle that can promote the innate ability of muscle to regenerate following volumetric muscle loss. Perfusion decellularization is an attractive technique for extracellular matrix (ECM) scaffold from intact mammalian organ or tissue which has been successfully used in tissue reconstruction. The perfusion-decellularization of skeletal muscle has been poorly assessed and characterized, but the bioactivity and functional capacity of the obtained perfusion skeletal muscle ECM (pM-ECM) to remodel in vivo is unknown. In the present study, pM-ECM was prepared from porcine rectus abdominis (RA). Perfusion-decellularization of porcine RA effectively removed cellular and nuclear material while retaining the intricate three-dimensional microarchitecture and vasculature networks of the native RA, and many of the bioactive ECM components and mechanical properties. In vivo, partial-thickness abdominal wall defects in rats repaired with pM-ECM showed improved neovascularization, myogenesis and functional recellularization compared to porcine-derived small intestinal submucosa (SIS). These findings show the biologic potential of RA pM-ECM as a scaffold for supporting site appropriate, tissue reconstruction, and provide a better understanding of the importance maintaining the tissue-specific complex three-dimensional architecture of ECM during decellularization and regeneration.

Original languageEnglish
Pages (from-to)114-126
Number of pages13
JournalBiomaterials
Volume89
DOIs
StatePublished - 1 May 2016
Externally publishedYes

Keywords

  • Abdominal defect repair
  • Extracellular matrix
  • Perfusion decellularization
  • Skeletal muscle
  • Three-dimensional scaffold
  • Volumetric muscle loss

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