iMacs are a versatile bridge between mechanistic immunology and next-generation translational medicine and enable large-scale production, precise genetic modification, and accurately mimic host-pathogen interactions, autoimmune phenotypes, metabolic inflammation, and tissue-specific macrophage functions.
A robust, reproducible, efficient serum-free and feeder-free protocol for generating functional iMacs and characterizing their innate immune properties, providing a versatile model for investigating innate immunity, host-pathogen interactions, and interferon signaling.
Hani Hosseini Far, Le Ying, L. Gearing et al.· Journal of Innate Immunity· 0 citations
A scalable, semi-automated, and physiologically relevant hiPSC-derived macrophage model, rigorously characterised through deep comparative multi-omics is established and how genetic perturbations alter pro- and anti-inflammatory transcriptional signatures and significantly impact functional phenotypes are showcased.
Mesenchymal stem cells (MSCs)/mesenchymal stromal cells and their extracellular vesicles (EVs), particularly exosomes, have emerged as therapeutic candidates in regenerative medicine due to their multipotency, low immunogenicity, and extensive immunomodulatory properties. This narrative review provides a narrative synt...
E. Ciarrochi, Juan B. Ciarrochi· Cureus· 0 citations
Liver fibrosis remains a major unmet clinical challenge characterized by persistent activation of hepatic stellate cells (HSCs), chronic inflammatory remodeling, and impaired hepatocyte regeneration. Although mesenchymal stem cell-derived extracellular vesicles (MSC-EVs) have emerged as promising cell-free therapeutics...
Fang-Hong Wang, Ke-Xiang Zhu, Xiao-Liang Zhu et al.· Frontiers in Bioengineering...· 0 citations