Bone Marrow Adipose Tissue and Skeletal Health

Shanmugam Muruganandan, Rajgopal Govindarajan, Christopher J. Sinal

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74 Citas (Scopus)

Resumen

Purpose of Review: To summarize and discuss recent progress and novel signaling mechanisms relevant to bone marrow adipocyte formation and its physiological/pathophysiological implications for bone remodeling. Recent Findings: Skeletal remodeling is a coordinated process entailing removal of old bone and formation of new bone. Several bone loss disorders such as osteoporosis are commonly associated with increased bone marrow adipose tissue. Experimental and clinical evidence supports that a reduction in osteoblastogenesis from mesenchymal stem cells at the expense of adipogenesis, as well as the deleterious effects of adipocyte-derived signaling, contributes to the etiology of osteoporosis as well as bone loss associated with aging, diabetes mellitus, post-menopause, and chronic drug therapy. However, this view is challenged by findings indicating that, in some contexts, bone marrow adipose tissue may have a beneficial impact on skeletal health. Summary: Further research is needed to better define the role of marrow adipocytes in bone physiology/pathophysiology and to determine the therapeutic potential of manipulating mesenchymal stem cell differentiation.

Idioma originalEnglish
Páginas (desde-hasta)434-442
Número de páginas9
PublicaciónCurrent Osteoporosis Reports
Volumen16
N.º4
DOI
EstadoPublished - ago. 1 2018

Nota bibliográfica

Funding Information:
Funding Information This work was supported by grants from the

Funding Information:
Canadian Institutes of Health Research and the National Sciences and Engineering Research Council of Canada (CJS) and the National Institutes of Health grants R03AR063326 (RG) and R01CA188464 (RG).

Publisher Copyright:
© 2018, Springer Science+Business Media, LLC, part of Springer Nature.

ASJC Scopus Subject Areas

  • Endocrinology, Diabetes and Metabolism

PubMed: MeSH publication types

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

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