Urinary bladder tissue engineering using natural scaffolds in a porcine model: role of Toll-like receptors and impact of biomimetic molecules

Cells Tissues Organs. 2010;192(4):250-61. doi: 10.1159/000317332. Epub 2010 Jun 30.

Abstract

Introduction: Natural scaffolds have been shown to induce T helper 2 (TH2)-specific immune responses in host tissues; however, the precise mechanisms that underlie this immune response are unknown. Using a porcine animal model, we evaluated the role of Toll-like receptors (TLRs) and matrix remodelling in the implantation of bladder acellular matrix (ACM) grafts and ACMs fortified with biomimetic materials.

Materials and methods: Bladders were decellularized with detergent and treated in 3 different ways prior to implantation: ACM alone, hyaluronic acid (HA)-ACM and HA-vascular endothelial growth factor (VEGF)-ACM. Animals were sacrificed at 4 or 10 weeks post-implantation and total gene expressions for TH2 (IL-4), TH1 (IFN-γ), TLR2, TLR4, and TGF-β1 were analyzed using real-time RT-PCR. Using histology (H&E and Masson's trichrome) and immunohistochemistry (uroplakin, α-smooth muscle actin, CD31 and factor VIII) the regenerative capacity was correlated with the gene expression of different proteins.

Results: IL-4, TLR2, and TLR4 gene expression were markedly decreased at 4 and 10 weeks in both the HA-ACM group and the HA-VEGF-ACM group compared to ACM alone. IFN-γ expression was negligible in all groups and time periods. TGF-β1 expression was highest in the HA- and VEGF-treated grafts. Recellularization was inversely proportional to TLR and TH2 expression but proportional to TGF-β1.

Conclusion: ACM alone grafts demonstrated stronger TLR4 expression which may promote a distinct TH2 immune response and a reduced regenerative capacity in grafts. Treatment of grafts with HA and VEGF may help regulate host immune responses by reducing TLR4 and IL-4 and increasing TGF-β1.

MeSH terms

  • Animals
  • Biomimetic Materials*
  • Cytokines / biosynthesis
  • Cytokines / metabolism
  • Extracellular Matrix
  • Gene Expression Regulation / drug effects
  • Guided Tissue Regeneration / methods*
  • Hyaluronic Acid / pharmacology
  • Interferon-gamma / metabolism
  • Interleukin-4 / metabolism
  • Macrophages
  • Neovascularization, Physiologic
  • Platelet Endothelial Cell Adhesion Molecule-1 / metabolism
  • Swine
  • Th2 Cells / immunology
  • Tissue Engineering*
  • Tissue Scaffolds*
  • Toll-Like Receptor 2 / metabolism
  • Toll-Like Receptor 4 / metabolism
  • Toll-Like Receptors / metabolism*
  • Transforming Growth Factor beta1 / metabolism
  • Up-Regulation
  • Urinary Bladder* / blood supply
  • Urinary Bladder* / immunology
  • Vascular Endothelial Growth Factor A / pharmacology

Substances

  • Cytokines
  • Platelet Endothelial Cell Adhesion Molecule-1
  • Toll-Like Receptor 2
  • Toll-Like Receptor 4
  • Toll-Like Receptors
  • Transforming Growth Factor beta1
  • Vascular Endothelial Growth Factor A
  • Interleukin-4
  • Interferon-gamma
  • Hyaluronic Acid