Sequential adaptation of perfusion and transport conditions significantly improves vascular construct recellularization and biomechanics

J Tissue Eng Regen Med. 2020 Mar;14(3):510-520. doi: 10.1002/term.3015. Epub 2020 Feb 6.

Abstract

Recellularization of ex vivo-derived scaffolds remains a significant hurdle primarily due to the scaffolds subcellular pore size that restricts initial cell seeding to the scaffolds periphery and inhibits migration over time. With the aim to improve cell migration, repopulation, and graft mechanics, the effects of a four-step culture approach were assessed. Using an ex vivo-derived vein as a model scaffold, human smooth muscle cells were first seeded onto its ablumen (Step 1: 3 hr) and an aggressive 0-100% nutrient gradient (lumenal flow under hypotensive pressure) was created to initiate cell migration across the scaffold (Step 2: Day 0 to 19). The effects of a prolonged aggressive nutrient gradient created by this single lumenal flow was then compared with a dual flow (lumenal and ablumenal) in Step 3 (Day 20 to 30). Analyses showed that a single lumenal flow maintained for 30 days resulted in a higher proportion of cells migrating across the scaffold toward the vessel lumen (nutrient source), with improved distribution. In Step 4 (Day 31 to 45), the transition from hypotensive pressure (12/8 mmHg) to normotensive (arterial-like) pressure (120/80 mmHg) was assessed. It demonstrated that recellularized scaffolds exposed to arterial pressures have increased glycosaminoglycan deposition, physiological modulus, and Young's modulus. By using this stepwise conditioning, the challenging recellularization of a vein-based scaffold and its positive remodeling toward arterial biomechanics were obtained.

Keywords: biomaterial; biomechanics; ex vivo-derived scaffold; recellularization; small diameter vascular graft; vascular tissue engineering; vascular wall.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biological Transport, Active
  • Blood Vessel Prosthesis*
  • Cell Survival
  • Extracellular Matrix / chemistry
  • Human Umbilical Vein Endothelial Cells / metabolism*
  • Humans
  • Myocytes, Smooth Muscle / metabolism*
  • Tissue Engineering*
  • Tissue Scaffolds / chemistry*