Induction of Human Embryonic and Induced Pluripotent Stem Cells Into Urothelium. (21st March 2014)

• Record Type: Journal Article
• Authors: Osborn, Stephanie L.; Thangappan, Ravikumar; Luria, Ayala; Lee, Justin H.; Nolta, Jan; Kurzrock, Eric A.
• Is Part Of: Stem cells translational medicine. Volume 3:Number 5(2014)
• Page Start: 610
• Page End: 619
• Publication Date: 2014-03-21
• Subjects: Embryonic stem cells -- Induced pluripotent stem cells -- Differentiation -- Urothelium -- Cancer; Stem cells -- Periodicals; Regenerative medicine -- Periodicals; Periodicals; 616.0277405
• DOI: 10.5966/sctm.2013-0131
• Languages: English
• ISSNs: 2157-6564

Abstract

Abstract : The current study demonstrates that derivation of urothelium from human embryonic stem cells (hESCs) and induced pluripotent stem cells (iPSCs) can be sufficiently accomplished in vitro in the absence of matrices, cell contact, or adult cell signaling and that the induction process appears to mimic normal differentiation. The ability to derive urothelium from nonautologous sources holds important implications for the bioengineering of bladder tissue for patients requiring urologic reconstruction. Abstract: In vitro generation of human urothelium from stem cells would be a major advancement in the regenerative medicine field, providing alternate nonurologic and/or nonautologous tissue sources for bladder grafts. Such a model would also help decipher the mechanisms of urothelial differentiation and would facilitate investigation of deviated differentiation of normal progenitors into urothelial cancer stem cells, perhaps elucidating areas of intervention for improved treatments. Thus far, in vitro derivation of urothelium from human embryonic stem cells (hESCs) or human induced pluripotent stem (hiPS) cells has not been reported. The goal of this work was to develop an efficient in vitro protocol for the induction of hESCs into urothelium through an intermediary definitive endoderm step and free of matrices and cell contact. During directed differentiation in a urothelial-specific medium ("Uromedium"), hESCs produced up to 60% urothelium, as determined by uroplakin expression; subsequent propagation selected for 90% urothelium. Alteration of the epithelial and mesenchymal cell signaling contribution through noncell contact coculture or conditioned media did not enhance the production of urothelium. Temporospatial evaluation of transcription factors known to be involved in urothelial specification showed association of IRF1, GET1, and GATA4 with uroplakin expression. Additional hESC and hiPS cell lines could also be induced into urothelium using this in vitro system. These results demonstrate that derivation and propagation of urothelium from hESCs and hiPS cells can be efficiently accomplished in vitro in the absence of matrices, cell contact, or adult cell signaling and that the induction process appears to mimic normal differentiation.