Chemico-Biological Interactions, Journal Year: 2024, Volume and Issue: unknown, P. 111319 - 111319
Published: Nov. 1, 2024
Language: Английский
Chemico-Biological Interactions, Journal Year: 2024, Volume and Issue: unknown, P. 111319 - 111319
Published: Nov. 1, 2024
Language: Английский
Veterinary Sciences, Journal Year: 2025, Volume and Issue: 12(3), P. 240 - 240
Published: March 3, 2025
MicroRNAs (miRNAs) are key regulators of gene expression, exerting post-translational control through mRNA silencing or degradation. These molecules play pivotal roles in host–pathogen interactions, particularly modulating antiviral immune responses. The global public health threat posed by the H5N1 Highly Pathogenic Avian Influenza (HPAI) virus necessitates urgent exploration novel therapeutic strategies. Our investigation revealed significant dysregulation miR-18a-5p following influenza infection, observed consistently across both vitro and vivo models. Experimental evidence demonstrated that overexpression effectively inhibits propagation multiple mechanisms: (1) studies using A549 cells transfected with mimics showed a substantial reduction viral replication; (2) animal models (mice chickens) elevated expression exhibited markedly suppressed AIV replication, reduced pathogenicity, improved survival rates. potential was evident its ability to significantly decrease mortality rates H5N1-infected animals. Furthermore, this miRNA robust protective effects against virus-induced lung damage, suggesting dual role preventing treating infections. findings position as promising candidate for development broad-spectrum interventions, offering strategic approach combat serious challenge.
Language: Английский
Citations
0Journal of the American Ceramic Society, Journal Year: 2025, Volume and Issue: unknown
Published: March 9, 2025
Abstract A simple 3D proliferation strategy for human umbilical cord‐derived mesenchymal stem cells (hUCMSCs) was developed based on porcine decellularized lung tissue microcarriers (DLTMs). The fixed with 75% ethanol, followed by decellularization and digestion pepsin‐acetic acid solution to form DLTMs an average diameter of 5–40 µm. presence key proteins, including collagen I, IV, laminin, fibronectin, elastin, confirmed through immunofluorescence staining, while the amount polysaccharides quantified. After centrifugation, hUCMSCs suspension formed spheroids which were cultured 14 days. Various techniques, DAPI, FDA H&E DNA quantification used assess performance hUCMSCs. Flow cytometric immunophenotyping employed, gene protein expressions cytokines growth factors such as IL‐10, HGF, KGF, Ang‐1 evaluated. results demonstrated that exhibited a porous structure simulated in vivo microenvironment, effectively enhancing immunomodulatory functions This showed potential integration bioreactor systems large‐scale production hUCMSC‐derived paracrine products therapeutic applications.
Language: Английский
Citations
0Chemico-Biological Interactions, Journal Year: 2024, Volume and Issue: unknown, P. 111319 - 111319
Published: Nov. 1, 2024
Language: Английский
Citations
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