4.7 Article

Ether-Oxygen Containing Electrospun Microfibrous and Sub-Microfibrous Scaffolds Based on Poly(butylene 1,4-cyclohexanedicarboxylate) for Skeletal Muscle Tissue Engineering

Journal

Publisher

MDPI
DOI: 10.3390/ijms19103212

Keywords

muscle tissue engineering; myogenesis; electrospinning; microfibres and sub-microfibres; biodegradable polyesters

Funding

  1. FWO [G060612N, G0A8813N, G088715N, 1525315N]
  2. CARIPLO Foundation [2015_0634]
  3. Opening the Future Campaign [EJJ-OPTFUT-02010]
  4. Excellentiefinanciering KULStem Cells [ETH-C1900-PF]
  5. Rondoufondsvoor Duchenne Onderzoek
  6. Belgian Agency for Science Policy [IUAPVII-07]
  7. FWO Post-Doctoral Fellowship [12D2813N]
  8. University of Pavia [AA 2013-2014]
  9. POR-FESR grant, Regione Emilia Romagna (University of Bologna)
  10. Italian Ministry of Education, University and Research (MIUR)
  11. FP7 COST Action [MP1206]

Ask authors/readers for more resources

We report the study of novel biodegradable electrospun scaffolds from poly(butylene 1,4-cyclohexandicarboxylate-co-triethylene cyclohexanedicarboxylate) (P(BCE-co-TECE)) as support for in vitro and in vivo muscle tissue regeneration. We demonstrate that chemical composition, i.e., the amount of TECE co-units (constituted of polyethylene glycol-like moieties), and fibre morphology, i.e., aligned microfibrous or sub-microfibrous scaffolds, are crucial in determining the material biocompatibility. Indeed, the presence of ether linkages influences surface wettability, mechanical properties, hydrolytic degradation rate, and density of cell anchoring points of the studied materials. On the other hand, electrospun scaffolds improve cell adhesion, proliferation, and differentiation by favouring cell alignment along fibre direction (fibre morphology), also allowing for better cell infiltration and oxygen and nutrient diffusion (fibre size). Overall, C2C12 myogenic cells highly differentiated into mature myotubes when cultured on microfibres realised with the copolymer richest in TECE co-units (micro-P73 mat). Lastly, when transplanted in the tibialis anterior muscles of healthy, injured, or dystrophic mice, micro-P73 mat appeared highly vascularised, colonised by murine cells and perfectly integrated with host muscles, thus confirming the suitability of P(BCE-co-TECE) scaffolds as substrates for skeletal muscle tissue engineering.

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