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1.
J Nanobiotechnology ; 22(1): 320, 2024 Jun 08.
Artículo en Inglés | MEDLINE | ID: mdl-38849820

RESUMEN

Simultaneously modulating the inflammatory microenvironment and promoting local bone regeneration is one of the main challenges in treating bone defects. In recent years, osteoimmunology has revealed that the immune system plays an essential regulatory role in bone regeneration and that macrophages are critical components. In this work, a mussel-inspired immunomodulatory and osteoinductive dual-functional hydroxyapatite nano platform (Gold/hydroxyapatite nanocomposites functionalized with polydopamine - PDA@Au-HA) is developed to accelerate bone tissues regeneration by regulating the immune microenvironment. PDA coating endows nanomaterials with the ability to scavenge reactive oxygen species (ROS) and anti-inflammatory properties, and it also exhibits an immunomodulatory ability to inhibit M1 macrophage polarization and activate M2 macrophage secretion of osteogenesis-related cytokines. Most importantly, this nano platform promotes the polarization of M2 macrophages and regulates the crosstalk between macrophages and pre-osteoblast cells to achieve bone regeneration. Au-HA can synergistically promote vascularized bone regeneration through sustained release of Ca and P particles and gold nanoparticles (NPs). This nano platform has a synergistic effect of good compatibility, scavenging of ROS, and anti-inflammatory and immunomodulatory capability to accelerate the bone repair process. Thus, our research offers a possible therapeutic approach by exploring PDA@Au-HA nanocomposites as a bifunctional platform for tissue regeneration.


Asunto(s)
Bivalvos , Regeneración Ósea , Durapatita , Oro , Indoles , Macrófagos , Osteogénesis , Regeneración Ósea/efectos de los fármacos , Durapatita/química , Durapatita/farmacología , Animales , Ratones , Oro/química , Oro/farmacología , Bivalvos/química , Células RAW 264.7 , Macrófagos/efectos de los fármacos , Indoles/química , Indoles/farmacología , Osteogénesis/efectos de los fármacos , Especies Reactivas de Oxígeno/metabolismo , Polímeros/química , Polímeros/farmacología , Nanocompuestos/química , Nanopartículas del Metal/química , Osteoblastos/efectos de los fármacos , Antiinflamatorios/farmacología , Antiinflamatorios/química , Factores Inmunológicos/farmacología , Factores Inmunológicos/química , Citocinas/metabolismo
2.
BMC Oral Health ; 23(1): 524, 2023 07 26.
Artículo en Inglés | MEDLINE | ID: mdl-37495990

RESUMEN

OBJECTIVE: Emerging evidence shows the clinical consequences of patient with COVID-19 and periodontitis are not promising, and periodontitis is a risk factor. Periodontitis and COVID-19 probably have a relationship. Hence, this study aimed to identify the common molecular mechanism that may help to devise potential therapeutic strategies in the future. MATERIAL AND METHODS: We analyzed two RNA-seq datasets for differential expressed genes, enrichment of biological processes, transcription factors (TFs) and deconvolution-based immune cell types in periodontitis, COVID-19 and healthy controls. Relationships between TFs and mRNA were established by Pearson correlation analysis, and the common TFs-mRNA regulatory network and nine co-upregulated TFs of the two diseases was obtained. The RT-PCR detected the TFs. RESULTS: A total of 1616 and 10201 differentially expressed gene (DEGs) from periodontitis and COVID-19 are found. Moreover, nine shared TFs and common biological processes associated with lymphocyte activation involved in immune response were identified across periodontitis and COVID-19. The cell type enrichment revealed elevated plasma cells among two diseases. The RT-PCR further confirmed the nine TFs up-regulation in periodontitis. CONCLUSION: The pathogenesis of periodontitis and COVID-19 is closely related to the expression of TFs and lymphocyte activation, which can provide potential targets for treatment.


Asunto(s)
COVID-19 , Periodontitis , Humanos , Perfilación de la Expresión Génica , Redes Reguladoras de Genes , Periodontitis/genética , Biomarcadores , ARN Mensajero
3.
Carbohydr Polym ; 346: 122656, 2024 Dec 15.
Artículo en Inglés | MEDLINE | ID: mdl-39245512

RESUMEN

The microenvironment of wound healing is susceptible to bacterial infection, chronic inflammation, oxidative stress, and inadequate angiogenesis, requiring the development of innovative wound dressings with antibacterial, anti-inflammatory, antioxidant, and angiogenic capabilities. This research crafted a new multifunctional bacterial cellulose composite membrane infused with copper-doped carbon dots (BC/Cu(II)-RCDs). Findings validated the successful loading of copper-doped carbon dots onto the BC membrane via hydrogen bonding interactions. Compared to the pure BC membrane, the BC/Cu(II)-RCDs composite membrane exhibited significantly enhanced hydrophilicity, tensile properties, and thermal stability. Diverse in vitro assays demonstrated excellent biocompatibility and antibacterial activity of BC/Cu(II)-RCDs composite membranes, alongside their ability to expedite the inflammatory phase and stimulate angiogenesis. In vivo trials corroborated the membrane's ability to foster epithelial regeneration, collagen deposition, and tissue regrowth in full-thickness skin wounds in rats while also curbing inflammation in infected full-thickness skin wounds. More importantly, the treatment of the BC/Cu(II)-RCDs composite membrane may result in the activation of VEGF and MAPK signaling proteins, which are key players in cell migration, angiogenesis, and skin tissue development. In essence, the developed BC/Cu(II)-RCDs composite membrane shows promise for treating infected wounds and serves as a viable alternative material for medicinal bandages.


Asunto(s)
Antibacterianos , Carbono , Celulosa , Cobre , Cicatrización de Heridas , Cicatrización de Heridas/efectos de los fármacos , Cobre/química , Celulosa/química , Celulosa/farmacología , Animales , Antibacterianos/farmacología , Antibacterianos/química , Carbono/química , Ratas , Humanos , Masculino , Ratas Sprague-Dawley , Staphylococcus aureus/efectos de los fármacos , Pruebas de Sensibilidad Microbiana , Puntos Cuánticos/química
4.
ACS Biomater Sci Eng ; 10(7): 4093-4113, 2024 Jul 08.
Artículo en Inglés | MEDLINE | ID: mdl-38829538

RESUMEN

Titanium (Ti) and its alloys are widely used biomaterials in bone repair. Although these biomaterials possess stable properties and good biocompatibility, the high elastic modulus and low surface activity of Ti implants have often been associated with infection, inflammation, and poor osteogenesis. Therefore, there is an urgent need to modify the surface of Ti implants, where changes in surface morphology or coatings loading can confer specific functions to help them adapt to the osseointegration formation phase and resist bacterial infection. This can further ensure a healthy microenvironment for bone regeneration as well as the promotion of immunomodulation, angiogenesis, and osteogenesis. Therefore, in this review, we evaluated various functional Ti implants after surface modification, both in terms of static modifications and dynamic response strategies, mainly focusing on the synergistic effects of antimicrobial activities and functionalized osteogenic. Finally, the current challenges and future perspectives are summarized to provide innovative and effective solutions for osseointegration and bone defect repair.


Asunto(s)
Antibacterianos , Oseointegración , Osteogénesis , Prótesis e Implantes , Propiedades de Superficie , Titanio , Titanio/química , Titanio/farmacología , Oseointegración/efectos de los fármacos , Humanos , Osteogénesis/efectos de los fármacos , Antibacterianos/farmacología , Antibacterianos/química , Animales , Materiales Biocompatibles Revestidos/química , Materiales Biocompatibles Revestidos/farmacología , Regeneración Ósea/efectos de los fármacos
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