Dual inhibition of TGFβR and ROCK reverses the epithelial to mesenchymal transition in collectively migrating zebrafish keratocytes

• Published in: Cell biology international 2021-06, Vol.45 (6), p.1288-1295
• Main Authors: Pascual, Agnes S., Rapanan, Jose L., Uppalapati, Chandana K., Cooper, Kimbal E., Leyva, Kathryn J., Hull, Elizabeth E.
• Format: Article
• Language: English
• Subjects: actin; Cell differentiation; Chronic illnesses; Danio rerio; Explants; Extracellular matrix; Fibroblasts; Fibrosis; Inflammation; Kinases; Localization; Mesenchyme; Progenitor cells; protein kinases/phosphatases; protein signaling modules/scaffolds; Snail protein; Stem cells; Transcription activation; Transcription factors; transcription/transcription factors; Transforming growth factor-b1; Wound healing
• ISSN: 1065-6995; 1095-8355
• DOI: 10.1002/cbin.11587

There is a growing controversy about the role of the epithelial to mesenchymal transition (EMT) in the fibrosis associated with chronic disease. Recent studies suggest that it is not the EMT transcriptional program but differentiation of progenitor cells, response to chronic inflammation, or some combination of both which cause the appearance of fibroblasts and the production of the extracellular matrix. To address this issue, we study the EMT process in the zebrafish keratocytes which migrate from primary explants of epithelial tissue as these cells are both terminally differentiated and able to divide. To firmly place this EMT process in the context of other systems, we first demonstrate that the zebrafish keratocyte EMT process involves nuclear accumulation of twist and snail/slug transcription factors as part of a TGFβR‐mediated EMT process. As assessed by the expression and localization of EMT transcription factors, the zebrafish keratocyte EMT process is reversed by the addition of Rho‐activated kinase (ROCK) in combination with TGFβR inhibitors. The complete cycle of EMT to MET observed in this system links these in vitro results more closely to the process of wound healing in vivo. However, the absence of observable activation of EMT transcription factors when keratocytes are cultured on compliant substrata in a TGFβ1‐containing medium suggests that ROCK signaling, initiated by tension within the sheet, is an essential contributor to the EMT process. Most importantly, the requirement for ROCK activation by culturing on noncompliant substrata suggests that EMT in these terminally differentiated cells would not occur in vivo.