AI Article Synopsis

  • Epithelial morphological changes and proliferation are critical for tubular structure formation, but the specific molecular mechanisms remain unclear.
  • Co-stimulation with Wnt3a and epidermal growth factor (EGF) promotes the development of intestinal epithelial cell tubes through the activation of the Arl4c protein, which isn't triggered by either factor alone.
  • Arl4c influences cytoskeletal rearrangement and cell growth by activating Rac and inactivating Rho, leading to the nuclear movement of YAP/TAZ, and is also involved in kidney development and organoid culture elongation.

Article Abstract

Growth factor-dependent epithelial morphological changes and proliferation are essential for the formation of tubular structures, but the underlying molecular mechanisms are poorly understood. Co-stimulation with Wnt3a and epidermal growth factor (Wnt3a/EGF) induced development of tubes consisting of intestinal epithelial cells by inducing expression of Arl4c, an Arf-like small GTP-binding protein, in three-dimensional culture, while stimulation with Wnt3a or EGF alone did not. Arl4c expression resulted in rearrangement of the cytoskeleton through activation of Rac and inactivation of Rho properly, which promoted cell growth by inducing nuclear translocation of Yes-associated protein and transcriptional co-activator with PDZ-binding motif (YAP/TAZ) in leading cells. Arl4c was expressed in ureteric bud tips and pretubular structures in the embryonic kidney. In an organoid culture assay, Wnt and fibroblast growth factor signaling simultaneously induced elongation and budding of kidney ureteric buds through Arl4c expression. YAP/TAZ was observed in the nucleus of extending ureteric bud tips. Thus, Arl4c expression induced by a combination of growth factor signaling mechanisms is involved in tube formation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4000088PMC
http://dx.doi.org/10.1002/embj.201386942DOI Listing

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