Helicoidal multi-lamellar features of RGD-functionalized silk biomaterials for corneal tissue engineering

Biomaterials. 2010 Dec;31(34):8953-63. doi: 10.1016/j.biomaterials.2010.08.017.

Abstract

RGD-coupled silk protein-biomaterial lamellar systems were prepared and studied with human cornea fibroblasts (hCFs) to match functional requirements. A strategy for corneal tissue engineering was pursued to replicate the structural hierarchy of human corneal stroma within thin stacks of lamellae-like tissues, in this case constructed from scaffolds constructed with RGD-coupled, patterned, porous, mechanically robust and transparent silk films. The influence of RGD-coupling on the orientation, proliferation, ECM organization, and gene expression of hCFs was assessed. RGD surface modification enhanced cell attachment, proliferation, alignment and expression of both collagens (type I and V) and proteoglycans (decorin and biglycan). Confocal and histological images of the lamellar systems revealed that the bio-functionalized silk human cornea 3D constructs exhibited integrated corneal stroma tissue with helicoidal multi-lamellar alignment of collagen-rich and proteoglycan-rich extracellular matrix, with transparency of the construct. This biomimetic approach to replicate corneal stromal tissue structural hierarchy and architecture demonstrates a useful strategy for engineering human cornea. Further, this approach can be exploited for other tissue systems due to the pervasive nature of such helicoids in most human tissues.

Publication types

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

MeSH terms

  • Biocompatible Materials / pharmacology*
  • Biomarkers / metabolism
  • Cell Differentiation / drug effects
  • Cell Differentiation / genetics
  • Cell Proliferation / drug effects
  • Cornea / drug effects
  • Cornea / physiology*
  • Corneal Stroma / cytology
  • Corneal Stroma / drug effects
  • Cytoskeleton / drug effects
  • Cytoskeleton / metabolism
  • DNA / metabolism
  • Extracellular Matrix / drug effects
  • Extracellular Matrix / metabolism
  • Gene Expression Regulation / drug effects
  • Humans
  • Oligopeptides / chemistry*
  • Protein Structure, Secondary
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Silk / chemistry*
  • Silk / pharmacology*
  • Tissue Engineering / methods*
  • Tissue Scaffolds / chemistry

Substances

  • Biocompatible Materials
  • Biomarkers
  • Oligopeptides
  • RNA, Messenger
  • Silk
  • arginyl-glycyl-aspartic acid
  • DNA