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From skeletal development to the creation of pluripotent stem cell-derived bone-forming progenitors.

Authors :
Wai Long Tam
Luyten, Frank P.
Roberts, Scott J.
Source :
Philosophical Transactions of the Royal Society B: Biological Sciences. 7/5/2018, Vol. 373 Issue 1750, p1-11. 11p.
Publication Year :
2018

Abstract

Bone has many functions. It is responsible for protecting the underlying soft organs, it allows locomotion, houses the bone marrow and stores minerals such as calcium and phosphate. Upon damage, bone tissue can efficiently repair itself. However, healing is hampered if the defect exceeds a critical size and/or is in compromised conditions. The isolation or generation of bone-forming progenitors has applicability to skeletal repair and may be used in tissue engineering approaches. Traditionally, bone engineering uses osteochondrogenic stem cells, which are combined with scaffold materials and growth factors. Despite promising preclinical data, limited translation towards the clinic has been observed to date. There may be several reasons for this including the lack of robust cell populations with favourable proliferative and differentiation capacities. However, perhaps the most pertinent reason is the failure to produce an implant that can replicate the developmental programme that is observed during skeletal repair. Pluripotent stem cells (PSCs) can potentially offer a solution for bone tissue engineering by providing unlimited cell sources at various stages of differentiation. In this review, we summarize key embryonic signalling pathways in bone formation coupled with PSC differentiation strategies for the derivation of bone-forming progenitors. This article is part of the theme issue 'Designer human tissue: coming to a lab near you'. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09628436
Volume :
373
Issue :
1750
Database :
Academic Search Index
Journal :
Philosophical Transactions of the Royal Society B: Biological Sciences
Publication Type :
Academic Journal
Accession number :
130649937
Full Text :
https://doi.org/10.1098/rstb.2017.0218