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Kidney development to kidney organoids and back again

期刊

SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
卷 127, 期 -, 页码 68-76

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2021.09.017

关键词

Kidney development; Stem cell; Kidney organoids; Metanephric mesenchyme; Ureteric bud; Nephron

资金

  1. National Institutes of Health (NIH) T32 fellowship training grant [DK007527]
  2. Harvard Stem Cell Institute interdisciplinary grant
  3. Brigham and Women's Hospital Research Excellence Award
  4. Brigham and Women's Hospital Faculty Career Development Award
  5. Harvard Stem Cell Institute Seed Grant
  6. DiaComp Pilot & Feasibility Program
  7. NIH [UC2DK126023, DP2EB029388, U01EB028899]

向作者/读者索取更多资源

The development of kidney organoid technology has revitalized the field of kidney developmental biology, allowing for the generation of nephron and collecting duct kidney organoids through directed differentiation protocols. However, there are limitations to current methods that need to be addressed for future improvements.
Kidney organoid technology has led to a renaissance in kidney developmental biology. The complex underpinnings of mammalian kidney development have provided a framework for the generation of kidney cells and tissues from human pluripotent stem cells. Termed kidney organoids, these 3-dimensional structures contain kidney-specific cell types distributed similarly to in vivo architecture. The adult human kidney forms from the reciprocal induction of two disparate tissues, the metanephric mesenchyme (MM) and ureteric bud (UB), to form nephrons and collecting ducts, respectively. Although nephrons and collecting ducts are derived from the intermediate mesoderm (IM), their development deviates in time and space to impart distinctive inductive signaling for which separate differentiation protocols are required. Here we summarize the directed differentiation protocols which generate nephron kidney organoids and collecting duct kidney organoids, making note of similarities as much as differences. We discuss limitations of these present approaches and discuss future directions to improve kidney organoid technology, including a greater understanding of anterior IM and its derivatives to enable an improved differentiation protocol to collecting duct organoids for which historic and future developmental biology studies will be instrumental.

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