Murine models of accelerated aging and musculoskeletal disease

William S. Hambright, Laura J. Niedernhofer, Johnny Huard, Paul D. Robbins

Research output: Contribution to journalArticle

Abstract

The primary risk factor for most musculoskeletal diseases, including osteoarthritis, osteoporosis and sarcopenia, is aging. To treat the diverse types of musculoskeletal diseases and pathologies, targeting their root cause, the aging process itself, has the potential to slow or prevent multiple age-related musculoskeletal conditions simultaneously. However, the development of approaches to delay onset of age related diseases, including musculoskeletal pathologies, has been slowed by the relatively long lifespan of rodent models of aging. Thus, to expedite the development of therapeutic approaches for age-related musculoskeletal disease, the implementation of mouse models of accelerated musculoskeletal aging are of great utility. Currently there are multiple genetically diverse mouse models that mirror certain aspects of normal human and mouse aging. Here, we provide a review of some of the most relevant murine models of accelerated aging that mimic many aspects of natural musculoskeletal aging, highlighting their relative strengths and weaknesses. Importantly, these murine models of accelerated aging recapitulate phenotypes of musculoskeletal age-related decline observed in humans.

Original languageEnglish (US)
Pages (from-to)122-127
Number of pages6
JournalBone
Volume125
DOIs
StatePublished - Aug 2019

Keywords

  • Accelerated aging
  • Mouse models
  • Musculoskeletal diseases
  • Progeria
  • Senescence
  • Stem cells

PubMed: MeSH publication types

  • Journal Article
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

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