Inferior In Vivo Osteogenesis and Superior Angiogenesis of Human Adipose‐Derived Stem Cells Compared with Bone Marrow‐Derived Stem Cells Cultured in Xeno‐Free Conditions.
Meadhbh A BrennanAudrey RenaudFabien GuillotonMiryam MebarkiValerie TrichetLuc SensebéFrederic DeschaseauxNathalie ChevallierPierre LayrollePublished in: Stem cells translational medicine (2017)
The possibility of using adipose tissue-derived stromal cells (ATSC) as alternatives to bone marrow-derived stromal cells (BMSC) for bone repair has garnered interest due to the accessibility, high cell yield, and rapid in vitro expansion of ATSC. For clinical relevance, their bone forming potential in comparison to BMSC must be proven. Distinct differences between ATSC and BMSC have been observed in vitro and comparison of osteogenic potential in vivo is not clear to date. The aim of the current study was to compare the osteogenesis of human xenofree-expanded ATSC and BMSC in vitro and in an ectopic nude mouse model of bone formation. Human MSC were implanted with biphasic calcium phosphate biomaterials in subcutis pockets for 8 weeks. Implant groups were: BMSC, ATSC, BMSC and ATSC mixed together in different ratios, as well as MSC primed with either osteogenic supplements (250 μM ascorbic acid, 10 mM β-glycerolphosphate, and 10 nM dexamethasone) or 50 ng/ml recombinant bone morphogenetic protein 4 prior to implantation. In vitro results show osteogenic gene expression and differentiation potentials of ATSC. Despite this, ATSC failed to form ectopic bone in vivo, in stark contrast to BMSC, although osteogenic priming did impart minor osteogenesis to ATSC. Neovascularization was enhanced by ATSC compared with BMSC; however, less ATSC engrafted into the implant compared with BMSC. Therefore, in the content of bone regeneration, the advantages of ATSC over BMSC including enhanced angiogenesis, may be negated by their lack of osteogenesis and prerequisite for osteogenic differentiation prior to transplantation. Stem Cells Translational Medicine 2017;6:2160-2172.
Keyphrases
- bone regeneration
- endothelial cells
- mesenchymal stem cells
- stem cells
- bone marrow
- gene expression
- adipose tissue
- mouse model
- cell therapy
- induced pluripotent stem cells
- bone mineral density
- soft tissue
- dna methylation
- pluripotent stem cells
- vascular endothelial growth factor
- magnetic resonance imaging
- metabolic syndrome
- photodynamic therapy
- insulin resistance
- high dose
- wound healing
- high fat diet
- human health
- climate change
- computed tomography
- bone loss
- clinical evaluation
- optical coherence tomography