Induced Pluripotent Stem Cell Derived Mesenchymal Stem Cells for Attenuating Age-Related Bone Loss

Abstract

Osteoporosis, both age-related and post-menopausal, is a huge health problem in the United States and indeed worldwide. Despite extensive research there remain few therapeutic approaches, with the exception of parathyroid hormone, that actually increase bone formation in osteoporotic patients. There are several limitations to the use of parathyroid hormone suggesting the need for continued research into anabolic therapies for osteoporosis. Mesenchymal stem cell (MSC) differentiation towards the bone forming osteoblastic lineage decreases as a function of age and may contribute to age-related bone loss. Therefore, MSC therapy may be beneficial in treating age-related bone loss. However, MSC availability decreases with age. To overcome the problem of age-related reduced availability of MSC we propose to examine the bone anabolic potential of induced pluripotent stem cell (iPS) derived MSC in age-related bone loss. Unfortunately deriving MSC from iPS can require extended in vitro culture, which decreases the differentiation potential of MSC. Since biomaterial surface characteristics, including stiffness and topography, can control MSC differentiation in vitro, including toward the osteoblastic lineage, the goal of this project is to identify biomaterial surface characteristics that enhance differentiation of iPS toward MSC and MSC toward osteoblastic cells. Our hypothesis is that culturing iPS on nanotopographic surfaces results in enrichment of a population of cells exhibiting MSC characteristics. Continued culture of these iPS derived MSC on nanotopographies results in increased osteoblastic differentiation and increased potential to induce bone formation in senescent accelerated mice (SAMP6), a murine model of age-induced bone loss. Successful completion of the specific aims would suggest a novel and highly innovative therapeutic approach to age-related osteoporosis.

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Document Details

Document Type
Technical Report
Publication Date
Jul 01, 2012
Accession Number
ADA581680

Entities

People

  • Henry J. Donahue

Organizations

  • Penn State Milton S. Hershey Medical Center

Tags

DTIC Thesaurus Topics

  • Availability
  • Biomaterials
  • Biomedical Research
  • Cells
  • Contracts
  • Hormones
  • Osteogenesis
  • Osteoporosis
  • Parathyroid Hormones
  • Peptide Growth Factors
  • Polymers
  • Stem Cells
  • Topography
  • United States

Fields of Study

  • Biology

Readers

  • Immunology and Pathology

Technology Areas

  • Biotechnology