About this Research Topic
In vivo experiments and clinical trials have demonstrated that MSC exert beneficial effects under several pathological conditions (GvHD, arteritis) through mechanisms of action are a direct consequence of their microenvironmental and/or systemic communication capacity. However, the MSC communication can be varied according to the physiological or pathophysiological situation and may include the secretion of small molecules, cytokines, adipokines, microRNA, and exosome/vesicles as well as direct cell-cell interactions mediated via surface receptors.
This Research Topic aims to provide a fundamental presentation of the current status of understanding relating to the MSC’s communication avenues in pathophysiological settings and relating these findings to their clinical translation.
• Soluble molecules for communication (small molecules, cytokines, adipokines)
• Microvesicles and exosomes
• Communication by contact (receptors and surface antigens)
• Exchange of biological materials (mitochondria)
• Communication of MSC and tissue repair
• Tissue-resident MSC and the diversity
• Native MSC communication
• Injected MSC communication
• Implications for clinical translation, manufacturing, and regulatory approval
Dr. Bourin works in a biotechnology company that develops a production process of ASC for clinical uses. Dr. Gimble is a co-founder, co-owner, and Chief Scientific Officer at Obatala Sciences and LaCell, biotechnology companies focused on the clinical translation of adipose-derived cells and tissues. The other Guest Editors declare no competing interests with regard to the Research Topic subject.
Keywords: MSC, Cell Communication, Microvesicules, Cell Therapy, Pathophysiology
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