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From Skeletal Development to the Creation of Pluripotent Stem Cell-derived Bone-forming Progenitors

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Specialty Biology
Date 2018 May 23
PMID 29786553
Citations 8
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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'.

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References
1.
Crane G, Jeffery E, Morrison S . Adult haematopoietic stem cell niches. Nat Rev Immunol. 2017; 17(9):573-590. DOI: 10.1038/nri.2017.53. View

2.
Lefebvre V, Behringer R, de Crombrugghe B . L-Sox5, Sox6 and Sox9 control essential steps of the chondrocyte differentiation pathway. Osteoarthritis Cartilage. 2001; 9 Suppl A:S69-75. DOI: 10.1053/joca.2001.0447. View

3.
Umeda K, Oda H, Yan Q, Matthias N, Zhao J, Davis B . Long-term expandable SOX9+ chondrogenic ectomesenchymal cells from human pluripotent stem cells. Stem Cell Reports. 2015; 4(4):712-26. PMC: 4400647. DOI: 10.1016/j.stemcr.2015.02.012. View

4.
Lefebvre V, Dvir-Ginzberg M . SOX9 and the many facets of its regulation in the chondrocyte lineage. Connect Tissue Res. 2016; 58(1):2-14. PMC: 5287363. DOI: 10.1080/03008207.2016.1183667. View

5.
Bruder S, Jaiswal N, Haynesworth S . Growth kinetics, self-renewal, and the osteogenic potential of purified human mesenchymal stem cells during extensive subcultivation and following cryopreservation. J Cell Biochem. 1997; 64(2):278-94. DOI: 10.1002/(sici)1097-4644(199702)64:2<278::aid-jcb11>3.0.co;2-f. View