2 research outputs found

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

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    Bone microenvironment; Bone regeneration; Multipotent mesenchymal stromal cellsMicroambient ossi; Regeneració òssia; Cèl·lules estromals mesenquimals multipotentsMicroambiente óseo; Regeneración ósea; Células estromales mesenquimales multipotentesBackground Wharton’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. Methods We 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. Results Co-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. Conclusions Our 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.This work was funded by CRG’s Emergent Translational Research Project Grant. Research in JV's laboratory is developed in the context of Red Española de Terapias Avanzadas (TERAV, expedient no. RD21/0017/0022) funded by Instituto de Salud Carlos III (ISCIII) in the context of NextGenerationEU's Recovery, Transformation and Resilience Plan, and has been recognised as a Consolidated Research Group by Generalitat de Catalunya (2021-SGR-00877). The disclosed funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

    Characterization of the Salinisation Processes in Aquifers Using Boron Isotopes; Application to South-Eastern Spain

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    Use of δ11B provides a solid tool for discriminating hydrogeochemical processes in complex coastal aquifers. Its efficiency increases markedly when it is applied along with other major or minor constituents. Nevertheless, various factors may affect its interpretation: the presence of clays, which favour adsorption and desorption, the influence of wastewaters, and even the presence of geothermalism. The δ11B has been applied to the study of a series of aquifers in south-eastern Spain: Castell de Ferro (Granada), Campo de Dalías, Lower Andarax and Sorbas (Almería), all of which are complex and heterogeneous. The results obtained demonstrate that the concentration of Br, the SO4/Cl and Cl/Br ratios are good indicators of marine intrusion. Inland some negative values of δ11B (−16.7 and −8.1‰) are related to a geothermal influence (34.8 and 51.5°C). The boron solubility is directly related to temperature favours boron mobilization, even from the associated metapelitic deposits. The difference in the boron isotope content in two carbonate units must be caused by the different composition of the carbonate rocks, as well as a long residence time
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