Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros











Intervalo de ano de publicação
1.
Int Immunopharmacol ; 130: 111713, 2024 Mar 30.
Artigo em Inglês | MEDLINE | ID: mdl-38387192

RESUMO

Asthma, a disease intricately linked to immune inflammation, is significantly influenced by the immune regulatory effect of bone mesenchymal stem cells (BMSCs). This study aims to investigate changes in the homing of BMSCs in bronchial asthma, focusing on the Notch homolog (Notch)1/Jagged1 signaling pathway's role in regulating T helper 1(Th1)/T helper 2(Th2) drift. Additionally, we further explore the effects and mechanisms of homologous BMSCs implantation in asthma-related immune inflammation. Following intervention with BMSCs, a significant improvement in the pathology of rats with asthma was observed. Simultaneously, a reduction in the expression of inflammatory cells and inflammatory cytokines, including tumor necrosis factor-α (TNF-α), interleukin(IL)-4, and IL-13 was observed in bronchoalveolar lavage fluid (BALF). Furthermore, there was an increase in the expression of Th1 cytokine Interferon-γ(IFN-γ)and the transcription factor T-box expressed in T cell (T-bet), while the expression of Th2 cytokine IL-13 and transcription factor GATA binding protein (GATA)-3 decreased in lung tissue. This indicates that the Th1/Th2 drift leans towards Th1, which a crucial in ameliorating asthma inflammation. Importantly, inhibition of the Notch1 signaling pathway led to an increased expression of the Stromal cell-derived factor-1(SDF-1)/C-X-C motif chemokine receptor (CXCR)4 chemokine axis. Consequently, the homing ability of bone marrow mesenchymal stem cells to asthma-affected lung tissue was significantly enhanced. BMSCs demonstrated heightened efficacy in regulating the cytokine/chemokine network and Th1/Th2 balance, thereby restoring a stable state during the immune response process in asthma. In conclusion, inhibiting the Notch signaling pathway enhances the expression of the SDF-1 and CXCR4 chemokine axis, facilitating the migration of allogeneic BMSCs to injured lung tissues. This, in turn, promotes immune regulation and improves the Th1/Th2 imbalance, thereby enhancing the therapeutic effect on asthmatic airway inflammation.


Assuntos
Asma , Células-Tronco Mesenquimais , Ratos , Animais , Camundongos , Interleucina-13/metabolismo , Asma/tratamento farmacológico , Pulmão/patologia , Citocinas/metabolismo , Transdução de Sinais , Fatores de Transcrição/metabolismo , Inflamação/metabolismo , Quimiocinas/metabolismo , Células-Tronco Mesenquimais/metabolismo , Células Th2 , Modelos Animais de Doenças , Camundongos Endogâmicos BALB C , Receptor Notch1/metabolismo
2.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-807275

RESUMO

Febrile seizures (FS) is the most common convulsive disorder in childhood and is a frequent problem for pediatricians.Most of the children have a good prognosis, but some children have recurrent attacks. Severe cases can even develop into epilepsy, which can cause great damage to the physical and mental health of children.Further understanding and studying issues related to febrile seizures has become a major concern for pediatricians and many families.This article reviews the definition, incidence, classification, etiology, pathogenesis, and epilepsy correlation and management measures of febrile seizures, and is expected to be applied in clinical practice to provide guidance for the prevention, diagnosis and treatment of febrile seizures.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA