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J Nanobiotechnology ; 22(1): 508, 2024 Aug 24.
Artigo em Inglês | MEDLINE | ID: mdl-39182069

RESUMO

Regenerating inflamed bone defects represents a severe clinical challenge due to the undesirable inflammatory microenvironment. The inflammatory stimulus poses a weighty threat to the regenerative capacity of endogenously derived mesenchymal stem cells (MSCs), which are mainly responsible for osteogenic differentiation, thereby resulting in compromised endogenous bone formation. Consequently, alleviating the biological characteristics of inflammatory-impaired MSCs is crucial for promoting inflamed bone regeneration. Nano-sized small extracellular vesicles (sEVs) have emerged as promising therapeutic tools to orchestrate MSCs fate due to their intrinsic biocompatibility and encapsulated bioactive contents. In the present study, we extracted sEVs from youthful and adult dental pulp MSCs and explored their ability to recover inflammation-compromised periodontal ligament stem cells (IPDLSCs). The results indicated that both types of sEVs were capable of facilitating IPDLSCs osteogenesis. However, young sEVs exhibited a more robust potential at a lower concentration compared to adult sEVs. Mechanically, young sEVs enhanced the expression of bone morphogenetic protein 4 (BMP4) via delivering the protein Biglycan, which correspondingly promoted the osteogenic capability of IPDLSCs. Collectively, our findings emphasized that young sEVs hold enormous potential to rescue the inherent function and regenerative competence of inflammation-impaired MSCs, shedding light on their promising therapeutic prospects for infected bone regeneration.


Assuntos
Biglicano , Regeneração Óssea , Diferenciação Celular , Vesículas Extracelulares , Células-Tronco Mesenquimais , Osteogênese , Ligamento Periodontal , Ligamento Periodontal/citologia , Ligamento Periodontal/metabolismo , Regeneração Óssea/efeitos dos fármacos , Biglicano/metabolismo , Vesículas Extracelulares/metabolismo , Osteogênese/efeitos dos fármacos , Humanos , Células-Tronco Mesenquimais/metabolismo , Inflamação/metabolismo , Proteína Morfogenética Óssea 4/metabolismo , Células Cultivadas , Polpa Dentária/citologia , Animais , Células-Tronco/metabolismo
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