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Related Concept Videos

Kidney Structure01:45

Kidney Structure

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The kidneys are two large bean-shaped organs located in the upper abdomen. They filter the blood several times a day to remove toxins and rebalance water and electrolytes of the circulatory system via the renal veins. The kidneys receive blood directly from the heart via the renal arteries. These arteries enter the kidney at the hilum, the concave surface of the bean, where they branch and divide into smaller vessels and capillaries.
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Related Experiment Video

Updated: Sep 29, 2025

Efficient Vascularization of Kidney Organoids through Intracelomic Transplantation in Chicken Embryos
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Studying Kidney Diseases Using Organoid Models.

Meng Liu1, Angelysia Cardilla1, Joanne Ngeow1,2

  • 1Lee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore, Singapore.

Frontiers in Cell and Developmental Biology
|March 21, 2022
PubMed
Summary
This summary is machine-generated.

Chronic kidney disease (CKD) is rising globally. Kidney organoids offer a promising new approach for modeling diseases and evaluating drugs, overcoming limitations of traditional methods.

Keywords:
PKDdifferentiationdisease modellingiPSCkidney diseasekidney organoidtubuloidtumoroid

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Area of Science:

  • Regenerative Medicine
  • Stem Cell Biology
  • Nephrology Research

Background:

  • Chronic kidney disease (CKD) prevalence is increasing globally, driven by diabetes and cardiovascular diseases.
  • Current therapeutic options like dialysis and transplantation have limitations, highlighting the need for novel treatment strategies.
  • Traditional research models (animal studies, cell cultures) face challenges in translation and maintaining cellular phenotypes.

Purpose of the Study:

  • To summarize current kidney organoid models.
  • To discuss advances in kidney disease modeling using organoids.
  • To identify challenges and propose solutions for applying organoids in disease modeling and drug evaluation.

Main Methods:

  • Generation of 3D kidney organoids from various cell sources, including human pluripotent stem cells (hPSCs).
  • Utilizing gene editing tools with hPSC-derived kidney organoids for modeling genetic kidney diseases.
  • Reviewing current literature on kidney organoid development and applications.

Main Results:

  • Successful generation of 3D kidney organoids from hPSCs, adult/fetal renal tissues, and kidney cancer biopsies.
  • hPSC-derived kidney organoids are being used to model genetic kidney diseases.
  • Adult kidney-derived tubuloids and kidney cancer-derived tumoroids are emerging models.

Conclusions:

  • Kidney organoids represent a significant advancement in understanding and modeling kidney diseases.
  • Further development is needed to overcome challenges in organoid application for disease modeling and drug screening.
  • Future solutions may enhance the utility of organoids in nephrology research and therapeutics.