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In this article, the authors showed that uPAR is expressed in senescence cells, both in in vivo and in vitro models (liver fibrosis, pancreatic intraepithelial neoplasia, senescent melanocytes, or lung cancer) correlated to a lack of expression in healthy tissue, except for the bronchial epithelium and a subset of immune cells in which a weak expression of uPAR was detected

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To explore whether VGF expression could increase -cell glucagon secretion, we constructed an adenovirus vector expressing VGF under the control of the glucagon promoter (Supplementary Fig