Human Wharton's jelly-derived mesenchymal stromal cells promote bone formation in immunodeficient mice when administered into a bone microenvironment

被引:3
作者
Cabrera-Perez, Raquel [1 ,2 ]
Rafols-Mitjans, Alexis [3 ]
Roig-Molina, Angela [2 ]
Beltramone, Silvia [3 ]
Vives, Joaquim [1 ,2 ,4 ]
Batlle-Morera, Laura [3 ]
机构
[1] Serv Terapia Cel<middle dot>lular i Avancada, Blood & Tissue Bank BST, Barcelona 08005, Catalonia, Spain
[2] Vall dHebron Res Inst VHIR, Musculoskeletal Tissue Engn Grp, Barcelona 08035, Catalonia, Spain
[3] Barcelona Inst Sci & Technol, Ctr Genom Regulat CRG, Gene Regulat Stem Cells & Canc Program, Barcelona 08003, Catalonia, Spain
[4] Univ Autonoma Barcelona UAB, Med Dept, Barcelona 08193, Catalonia, Spain
关键词
Advanced therapy medicinal product; Bone microenvironment; Bone regeneration; Regenerative medicine; Multipotent mesenchymal stromal cells; Wharton's jelly; STEM-CELLS; ADIPOSE-TISSUE; MARROW; DIFFERENTIATION; THERAPY; DISEASE;
D O I
10.1186/s12967-023-04672-9
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundWharton's Jelly (WJ) Mesenchymal Stromal Cells (MSC) have emerged as an attractive allogeneic therapy for a number of indications, except for bone-related conditions requiring new tissue formation. This may be explained by the apparent recalcitrance of MSC,WJ to differentiate into the osteogenic lineage in vitro, as opposed to permissive bone marrow (BM)-derived MSCs (MSC,BM) that readily commit to bone cells. Consequently, the actual osteogenic in vivo capacity of MSC,WJ is under discussion.MethodsWe investigated how physiological bone environments affect the osteogenic commitment of recalcitrant MSCs in vitro and in vivo. To this end, MSC of BM and WJ origin were co-cultured and induced for synchronous osteogenic differentiation in vitro using transwells. For in vivo experiments, immunodeficient mice were injected intratibially with a single dose of human MSC and bone formation was evaluated after six weeks.ResultsCo-culture of MSC,BM and MSC,WJ resulted in efficient osteogenesis in both cell types after three weeks. However, MSC,WJ failed to commit to bone cells in the absence of MSC,BM's osteogenic stimuli. In vivo studies showed successful bone formation within the medullar cavity of tibias in 62.5% of mice treated with MSC, WJ. By contrast, new formed trabeculae were only observed in 25% of MSC,BM-treated mice. Immunohistochemical staining of human COXIV revealed the persistence of the infused cells at the site of injection. Additionally, cells of human origin were also identified in the brain, heart, spleen, kidney and gonads in some animals treated with engineered MSC,WJ (eMSC,WJ). Importantly, no macroscopic histopathological alterations, ectopic bone formation or any other adverse events were detected in MSC-treated mice.ConclusionsOur findings demonstrate that in physiological bone microenvironment, osteogenic commitment of MSC,WJ is comparable to that of MSC,BM, and support the use of off-the-shelf allogeneic MSC,WJ products in bone repair and bone regeneration applications.
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页数:12
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