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Related Concept Videos

Anatomy of the Genitourinary System I: Kidneys and Ureters01:11

Anatomy of the Genitourinary System I: Kidneys and Ureters

155
The upper urinary system comprises two kidneys and two ureters, which are crucial in filtering blood and forming urine.KidneysLocation and Structure:The kidneys are two bean-shaped organs positioned behind the peritoneum on either side of the spine.Kidneys are between the 12th thoracic (T12) and the 3rd lumbar (L3) vertebrae.The position of the liver causes the right kidney to sit slightly lower than the left.Protective Layers:Each kidney is enveloped in a tough, fibrous membrane called the...
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Ureters01:22

Ureters

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The ureters are retroperitoneal tubes located on either side of the vertebral column. They are responsible for transporting urine from each kidney to the urinary bladder. These tubes have thick walls and are approximately 25-30 cm long. Their diameter is around 10 mm at the renal pelvis, gradually narrowing to 1 mm as the ureter obliquely enters the posterior bladder wall through the ureteric orifices. The shape of these orifices is slit-like, which helps to prevent urine backflow toward the...
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Renal Tubule and Collecting Duct01:24

Renal Tubule and Collecting Duct

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The renal tubule is divided into three parts: the proximal convoluted tubule (PCT), the Loop of Henle (LOH), and the distal convoluted tubule (DCT).
Proximal Convoluted Tubule (PCT):
The PCT is the initial segment of the renal tubule, extending from the Bowman's capsule that encloses the glomerulus. Its convoluted structure and microvilli-lined cells increase the surface area for reabsorption. The PCT reabsorbs glucose, amino acids, sodium, and water from the filtrate, ensuring essential...
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Related Experiment Video

Updated: Oct 11, 2025

Development of Human Renal Tubular Epithelial Cell Primary Cultures in Monolayers and Three-Dimensional Conditions
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Development of Human Renal Tubular Epithelial Cell Primary Cultures in Monolayers and Three-Dimensional Conditions

Published on: June 13, 2025

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Building human renal tracts.

Adrian S Woolf1

  • 1Division of Cell Matrix Biology and Regenerative Medicine, School of Biological Sciences, Michael Smith Building, Faculty of Biology Medicine and Health, University of Manchester, Oxford Road, Manchester, Northern Ireland M13 9PT, United Kingdom; Royal Manchester Children's Hospital, Manchester University NHS Foundation Trust, Manchester Academic Health Science Center, Manchester, Northern Ireland, United Kingdom.

Journal of Pediatric Surgery
|November 28, 2021
PubMed
Summary
This summary is machine-generated.

Researchers are developing functional kidney tissues from human pluripotent stem cells for regenerative medicine. While organoids show promise, challenges like vascularization and urinary tract integration must be addressed for clinical application.

Keywords:
Collecting ductImplantNephronPluripotent stem cellUreter

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Area of Science:

  • Regenerative Medicine
  • Developmental Biology
  • Genetics

Background:

  • Millions worldwide suffer from severe kidney failure, including children with congenital renal tract abnormalities.
  • Limited kidney transplant availability and long-term dialysis pose significant challenges, failing to fully mitigate uraemia.
  • Advancements in stem cell technology, developmental biology, and genetics offer potential for novel kidney disease therapies.

Purpose of the Study:

  • To review progress in generating functional kidney tissues from human pluripotent stem cells.
  • To explore the potential of pluripotent stem cell-derived kidney organoids for regenerative medicine.
  • To identify current limitations and future directions for clinical applications.

Main Methods:

  • Generation of kidney organoids from human pluripotent stem cells in culture.
  • Enhancement of organoid differentiation through implantation into immunodeficient mice.
  • Utilizing pluripotent stem cell technology to create 'diseases in a dish' models.

Main Results:

  • Pluripotent stem cells can form organoids containing immature glomeruli and tubules.
  • In vivo implantation improves the differentiation of kidney organoids.
  • Pluripotent stem cell models aid in understanding the pathobiology of renal tract malformations.

Conclusions:

  • Human pluripotent stem cell-derived kidney organoids represent a promising step towards regenerative therapies for kidney failure.
  • Overcoming limitations such as organoid size, vascularization, and urinary tract integration is crucial for clinical translation.
  • Stem cell-based disease models are valuable tools for investigating congenital kidney diseases.