Development, structure, and bioengineering of the human corneal stroma: A review of collagen-based implants

• Published in: Experimental eye research 2020-11, Vol.200, p.108256-108256, Article 108256
• Main Authors: Tidu, Aurélien, Schanne-Klein, Marie-Claire, Borderie, Vincent M.
• Format: Article
• Language: English
• Subjects: Animals; Artificial cornea; Bioengineering - methods; Collagen; Collagen - pharmacology; Cornea development; Corneal Stroma - cytology; Corneal Stroma - growth & development; Corneal Stroma - metabolism; Drug Implants; Humans; Keratocytes; Mesenchymal Stem Cells - cytology; Recombinant Proteins; Stromal structure
• ISSN: 0014-4835; 1096-0007
• DOI: 10.1016/j.exer.2020.108256

Bio-engineering technologies are currently used to produce biomimetic artificial corneas that should present structural, chemical, optical, and biomechanical properties close to the native tissue. These properties are mainly supported by the corneal stroma which accounts for 90% of corneal thickness and is mainly made of collagen type I. The stromal collagen fibrils are arranged in lamellae that have a plywood-like organization. The fibril diameter is between 25 and 35 nm and the interfibrillar space about 57 nm. The number of lamellae in the central stroma is estimated to be 300. In the anterior part, their size is 10–40 μm. They appear to be larger in the posterior part of the stroma with a size of 60–120 μm. Their thicknesses also vary from 0.2 to 2.5 μm. During development, the acellular corneal stroma, which features a complex pattern of organization, serves as a scaffold for mesenchymal cells that invade and further produce the cellular stroma. Several pathways including Bmp4, Wnt/β-catenin, Notch, retinoic acid, and TGF-β, in addition to EFTFs including the mastering gene Pax-6, are involved in corneal development. Besides, retinoic acid and TGF- β seem to have a crucial role in the neural crest cell migration in the stroma. Several technologies can be used to produce artificial stroma. Taking advantage of the liquid-crystal properties of acid-soluble collagen, it is possible to produce transparent stroma-like matrices with native-like collagen I fibrils and plywood-like organization, where epithelial cells can adhere and proliferate. Other approaches include the use of recombinant collagen, cross-linkers, vitrification, plastically compressed collagen or magnetically aligned collagen, providing interesting optical and mechanical properties. These technologies can be classified according to collagen type and origin, presence of telopeptides and native-like fibrils, structure, and transparency. Collagen matrices feature transparency >80% for the appropriate 500-μm thickness. Non-collagenous matrices made of biopolymers including gelatin, silk, or fish scale have been developed which feature interesting properties but are less biomimetic. These bioengineered matrices still need to be colonized by stromal cells to fully reproduce the native stroma. •During development, mesenchymal cells invade the organized acellular corneal stroma and further produce the cellular stroma.•Collagen liquid-crystal properties permit producing transparent matrices with col