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Image Search Results
Journal: Cell Communication and Signaling : CCS
Article Title: Hippo pathway suppression reprograms TNFα-primed glioblastoma extracellular vesicles transcripts cargo to drive mesenchymal stem/stromal cells vasculogenic mimicry
doi: 10.1186/s12964-025-02401-x
Figure Lengend Snippet: VT107 alters the capacity of extracellular vesicles isolated from TNFα-treated U87 glioblastoma cells to trigger in vitro mesenchymal stem cells vasculogenic mimicry. ( A ) Representative phase contrast images were taken to monitor the formation of mesenchymal stem/stromal cells capillary-like structures for up to 6 h (upper panels) and were analyzed via Wimasis (lower panels). ( B ) Quantification from Wimasis analysis of the total loops over time. ( C ) Cultrex was depleted from soluble growth factors, then used to monitor the capacity to re-induce capillary-like structure formation upon 6 h (upper panels). The structures were analyzed via Wimasis (lower panels). Total loops were quantified to assess in vitro VM. ( D ) The impact of serum-free media (closed triangles), EVs (open circles) and of serum-enriched media (closed circles), or ( E ) the impact of EVs isolated from control, 30 ng/ml TNFα-, 1 µM VT107-, or TNFα/VT107-treated cells, was assessed on in vitro VM
Article Snippet: VM was assessed in vitro using
Techniques: Isolation, In Vitro, Control
Journal: Journal of Virology
Article Title: Development of a Primary Human Cell Model for the Study of Human Cytomegalovirus Replication and Spread within Salivary Epithelium
doi: 10.1128/JVI.01608-18
Figure Lengend Snippet: Establishment of salispheres and primary epithelial lines from human salivary gland. (A) Freshly isolated salivary gland tissues (top) were digested with collagenase-dispase, and single-cell suspensions were then cultured on Cultrex PathClear basement membrane extract (BME) gels, where multicellular salispheres developed within 72 to 96 h (middle). Salispheres were then dissociated, counted, and replated onto Cultrex PathClear BME gels as in the middle panel or plated onto plastic culture dishes to facilitate HCMV infection experiments (bottom). (B) Salispheres were used for mRNA preparation and amylase 1 and hypoxanthine-guanine phosphotransferase (HPRT) expression. (C) Salispheres were then used for more-detailed analyses of salivary gland-specific gene expression. Taken together, the results indicate that the salispheres grown in vitro exhibit gene expression profiles similar to those of salivary tissue in vivo.
Article Snippet: Following digestion and lysis of red blood cells, the salivary cells were plated on
Techniques: Isolation, Cell Culture, Membrane, Infection, Expressing, Gene Expression, In Vitro, In Vivo