Development and differentiation of the ureteric bud into the ureter in the absence of a kidney collecting system.

Dev Biol

Department of Medicine, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0693, and Urological Diseases Research Center, Department of Urology, Children's Hospital, Boston, MA 02115, USA.

Published: October 2006

Six1-/- mice were found to have apparently normal ureters in the absence of a kidney, suggesting that the growth and development of the unbranched ureter is largely independent of the more proximal portions of the UB which differentiates into the highly branched renal collecting system. Culture of isolated urinary tracts (from normal and mutant mice) on Transwell filters was employed to study the morphogenesis of this portion of the urogenital system. Examination of the ureters revealed the presence of a multi-cell layered tubule with a lumen lined by cells expressing uroplakin (a protein exclusively expressed in the epithelium of the lower urinary tract). Cultured ureters of both the wild-type and Six1 mutant become contractile and undergo peristalsis, an activity preceded by the expression of alpha-smooth muscle actin (alphaSMA). Treatment with a number of inhibitors of signaling molecules revealed that inhibition of PI3 kinase dissociates the developmental expression of alphaSMA from ureter growth and elongation. Epidermal growth factor also perturbed smooth muscle differentiation in culture. Moreover, the peristalsis of the ureter in the absence of the kidney in the Six1-/- mouse indicates that the development of this clinically important function of ureter (peristaltic movement of urine) is not dependent on fluid flow through the ureter. In keeping with this, isolated ureters cultured in the absence of surrounding tissues elongate, differentiate and undergo peristalsis when cultured on a filter and undergo branching morphogenesis when cultured in 3-dimensional extracellular matrix gels in the presence of a conditioned medium derived from a metanephric mesenchyme (MM) cell line. In addition, ureters of Six1-/- urinary tracts (i.e., lacking a kidney) displayed budding structures from their proximal ends when cultured in the presence of GDNF and FGFs reminiscent of UB budding from the wolffian duct. Taken together with the above data, this indicates that, although the distal ureter (at least early in its development) retains some of the characteristics of the more proximal UB, the growth and differentiation (i.e., development of smooth muscle actin, peristalsis and uroplakin expression) of the distal non-branching ureter are inherent properties of this portion of the UB, occurring independently of detectable influences of either the undifferentiated MM (unlike the upper portion of the ureteric bud) or more differentiated metanephric kidney. Thus, the developing distal ureter appears to be a unique anatomical structure which should no longer be considered as simply the non-branching portion of the ureteric bud. In future studies, the ability to independently analyze and study the portion of the UB that becomes the renal collecting system and that which becomes the ureter should facilitate distinguishing the developmental nephrome (renal ontogenome) from the ureterome.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ydbio.2006.07.006DOI Listing

Publication Analysis

Top Keywords

ureteric bud
12
absence kidney
12
collecting system
12
ureter
10
ureter absence
8
renal collecting
8
urinary tracts
8
undergo peristalsis
8
muscle actin
8
smooth muscle
8

Similar Publications

Article Synopsis
  • Scientists are studying how tiny structures in the kidneys form during development, especially how they branch out and work together.
  • They discovered that as these structures grow, they get packed tightly together, which can change how the cells make decisions.
  • The researchers used experiments and math to understand this packing and found that it affects how the kidneys develop over time in mice and might help in creating new tissues for medical purposes.
View Article and Find Full Text PDF

The kidney maintains homeostasis through an array of parallel nephrons, which all originate in development as isolated epithelial structures that later fuse through their distal poles to a system of collecting ducts (CD). This connection is required to generate functional nephrons by providing a pathway for excretion of metabolic waste and byproducts. Currently, methods for differentiating human pluripotent stem cells into kidney organoids generate nephrons that lack CDs and instead terminate as blind-ended tubules.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates the Wnt/β-catenin signaling pathway's impact on gene expression in different embryonic kidney cell types, emphasizing its significance in kidney development.
  • Researchers activated the signaling in mouse kidneys and performed RNA sequencing, identifying 917 differentially expressed genes (DEGs), connected to kidney development and immune responses.
  • The findings offer insights into gene expression variations in specific kidney cell types, revealing key genes affected by Wnt/β-catenin signaling, which could inform future research on kidney development and related diseases.
View Article and Find Full Text PDF

Introduction: Zinner Syndrome (ZS) is a rare congenital disorder characterized by seminal vesicle cysts (SVC) and ipsilateral upper urinary tract abnormalities, mainly due to developmental anomalies of the mesonephric duct. This series highlights our institutional experience with pediatric ZS, with a review of the current literature offering insights into its etiopathogenesis in early childhood.

Material And Methods: A retrospective case review of pediatric ZS diagnosed at our institution from 2019 to 2023, alongside a comprehensive literature review.

View Article and Find Full Text PDF

Generating kidney organoids based on developmental nephrology.

Eur J Cell Biol

December 2024

Department of Kidney Development, Institute of Molecular Embryology and Genetics, Kumamoto University, Kumamoto, Japan. Electronic address:

Over the past decade, the induction protocols for the two types of kidney organoids (nephron organoids and ureteric bud organoids) from pluripotent stem cells (PSCs) have been established based on the knowledge gained in developmental nephrology. Kidney organoids are now used for disease modeling and drug screening, but they also have potential as tools for clinical transplantation therapy. One of the options to achieve this goal would be to assemble multiple renal progenitor cells (nephron progenitor, ureteric bud, stromal progenitor) to reproduce the organotypic kidney structure from PSCs.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!