4.5 Article

Adult stem cell driven genesis of human-shaped articular condyle

Journal

ANNALS OF BIOMEDICAL ENGINEERING
Volume 32, Issue 7, Pages 911-923

Publisher

SPRINGER
DOI: 10.1023/B:ABME.0000032454.53116.ee

Keywords

mesenchymal; cartilage; bone; tissue engineering; stem cell; osteochondral; hydrogel

Funding

  1. NIAMS NIH HHS [AR048316] Funding Source: Medline
  2. NIA NIH HHS [AG00010] Funding Source: Medline
  3. NIBIB NIH HHS [EB02332] Funding Source: Medline
  4. NIDCR NIH HHS [DE00722, DE13964] Funding Source: Medline

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Uniform design of synovial articulations across mammalian species is challenged by their common susceptibility to joint degeneration. The present study was designed to investigate the possibility of creating human-shaped articular condyles by rat bone marrow-derived mesenchymal stem cells (MSCs) encapsulated in a biocompatible poly(ethylene glycol)-based hydrogel. Rat MSCs were harvested, expanded in culture, and treated with either chondrogenic or osteogenic supplements. Rat MSC-derived chondrogenic and osteogenic cells were loaded in hydrogel suspensions in two stratified and yet integrated hydrogel layers that were sequentially photopolymerized in a human condylar mold. Harvested articular condyles from 4-week in vivo implantation demonstrated stratified layers of chondrogenesis and osteogenesis. Parallel in vitro experiments using goat and rat MSCs corroborated in vivo data by demonstrating the expression of chondrogenic and osteogenic markers by biochemical and mRNA analyses. Ex vivo incubated goat MSC-derived chondral constructs contained cartilage-related glycosaminoglycans and collagen. By contrast, goat MSC-derived osteogenic constructs expressed alkaline phosphatase and osteonectin genes, and showed escalating calcium content over time. Rat MSC-derived osteogenic constructs were stiffer than rat MSC-derived chondrogenic constructs upon nanoindentation with atomic force microscopy. These findings may serve as a primitive proof of concept for ultimate tissue-engineered replacement of degenerated articular condyles via a single population of adult mesenchymal stem cells.

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