• Media type: Text; Doctoral Thesis; Electronic Thesis; E-Book
  • Title: Molecular control of murine ureter development - the function of FGF and BMP4 signaling
  • Contributor: Deuper, Lena [Author]
  • Published: Hannover : Institutionelles Repositorium der Leibniz Universität Hannover, 2023
  • Issue: published Version
  • Language: English
  • DOI: https://doi.org/10.15488/13536; https://doi.org/10.1242/dev.200021; https://doi.org/10.1242/dev.200767
  • Keywords: Urothel ; urothelium ; lamina propria ; FGF ; glatte Muskulatur ; SMC ; ureter ; Differenzierung ; BMP4 ; differentiation
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  • Description: The ureters are muscular tubes that propel the urine from the renal pelvis to the bladder by uni-directional peristaltic contractions. To fulfill this function the ureters are compartmentalized into an outer mesenchymal wall with layers of fibrocytes in the inner lamina propria (LP) and the outer tunica adventitia (TA) unsheathing smooth muscle cells (SMC), and an inner highly spe-cialized epithelium: the urothelium. The urothelium features a three-layered organization of su-perficial (S), intermediate (I) and basal (B) cells. The ureteric mesenchyme (UM) as well as the ureteric epithelium (UE) arise from pools of homogeneous, uncommitted precursor cells. Pat-terning, proliferation and differentiation of these progenitors rely on a very complex interplay of various signaling pathways. SHH and WNT signals from the UE and BMP4 from the UM pro-mote epithelial and mesenchymal proliferation and differentiation. In contrast, retinoic acid (RA) within the UM and the UE inhibits differentiation and promotes precursor proliferation in both compartments. How these signals cooperate with each other and possibly additional as yet unknown signals and how they impinge on various transcription factor (TF) genes to control the development of three different cell types from homogeneous precursor cell populations in two different tissue compartments is poorly understood. Aim of this thesis was to address the func-tion of FGF and BMP4 signaling in this context. Expression of Fgfr1 and Fgfr2 was found in the undifferentiated UE as well as in the surround-ing UM. Targeted inactivation of Fgfr2 in the UE resulted in loss of I and B cells, delayed onset of SMC differentiation and in an inability to form the LP. Fgfr2 was found to increase SHH and BMP4 signaling to allow differentiation of epithelial cells and to precisely activate SMC differen-tiation. FGFRs in the mesenchyme act as a molecular sink to fine tune this signaling axis. Tar-geted ablation of Fgfr1 and Fgfr2 delayed the onset of SMC differentiation and led to premature ...
  • Access State: Open Access