Classically, fibroblasts are defined as non-epithelial, nonimmune cells of mesenchymal origin with a spindle-shaped morphology, dwelling in interstitial spaces or near blood vessels, and capable of extracellular matrix (ECM) deposition and remodeling. 1 Embedded in the tissue parenchyma, fibroblasts are active participants in biological processes not only by shaping tissue architecture via ECM remodeling, but also through regulating immune cell recruitment, wound-healing responses, inflammation, and fibrosis. 2-4 Recent reviews 1 have proposed an organizational framework chiefly consisting of the following flavors of fibroblasts: (a) spindle-shaped quiescent or resting fibroblasts that are metabolically inactive and occupy the interstitial space in the ECM; (b) stellate-shaped normal activated fibroblasts (NAFs), which are epigenetically reversible, and influenced by various stimuli such as stress, wounding, and inflammation; and (c) cancer-associated fibroblasts or fibrosis-associated fibroblasts (CAFs or FAFs), which are generated in response to unrelenting chronic stimuli