Kidney disease is a global health crisis affecting more than 850 million people worldwide. In the United States, annual Medicare expenditures for kidney disease and organ failure exceed $81 billion. Efforts to develop targeted therapeutics are limited by a poor understanding of the molecular mechanisms underlying human kidney disease onset and progression. Additionally, 90% of drug candidates fail in human clinical trials, often due to toxicity and efficacy not accurately predicted in animal models.The advent of ex vivo kidney models, such as those engineered from induced pluripotent stem (iPS) cells and organ-on-a-chip (organ-chip) systems, has garnered considerable interest owing to their ability to more accurately model tissue development and patient-specific responses and drug toxicity. This review describes recent advances in developing kidney organoids and organ-chips by harnessing iPS cell biology to model human-specific kidney functions and disease states. We also discuss challenges that must be overcome to realize the potential of organoids and organ-chips as dynamic and functional conduits of the human kidney. Achieving these technological advances could revolutionize personalized medicine applications and therapeutic discovery for kidney disease.
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Lawrence J Ellison Inst Transformat Med, Los Angeles, CA 90064 USALawrence J Ellison Inst Transformat Med, Los Angeles, CA 90064 USA
Strelez, Carly
Jiang, Hannah Y.
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Lawrence J Ellison Inst Transformat Med, Los Angeles, CA 90064 USA
Univ Southern Calif, Viterbi Sch Engn, Dept Biomed Engn, Los Angeles, CA 90089 USALawrence J Ellison Inst Transformat Med, Los Angeles, CA 90064 USA
Jiang, Hannah Y.
Mumenthaler, Shannon M.
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Lawrence J Ellison Inst Transformat Med, Los Angeles, CA 90064 USA
Univ Southern Calif, Viterbi Sch Engn, Dept Biomed Engn, Los Angeles, CA 90089 USA
Univ Southern Calif, Norris Comprehens Canc Ctr, Keck Sch Med, Dept Oncol, Los Angeles, CA 90033 USALawrence J Ellison Inst Transformat Med, Los Angeles, CA 90064 USA
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Leiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, NetherlandsLeiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
Tang, Huaqi
Abouleila, Yasmine
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Leiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, NetherlandsLeiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
Abouleila, Yasmine
Si, Longlong
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Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USALeiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
Si, Longlong
Ortega-Prieto, Ana Maria
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Imperial Coll London, Dept Med, Sect Virol, London W2 1PG, EnglandLeiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
Ortega-Prieto, Ana Maria
Mummery, Christine L.
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Leiden Univ, Dept Anat & Embryol, Med Ctr, Einthovenweg 20, NL-2333 ZD Leiden, NetherlandsLeiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, Netherlands
Mummery, Christine L.
Ingber, Donald E.
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Harvard Univ, Wyss Inst Biol Inspired Engn, Boston, MA 02115 USA
Harvard Univ, Harvard John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
Harvard Med Sch, Vasc Biol Program, Boston, MA 02115 USA
Harvard Med Sch, Dept Surg, Boston, MA 02115 USA
Boston Childrens Hosp, Boston, MA 02115 USALeiden Univ, Leiden Acad Ctr Drug Res, Med Syst Biophys & Bioengn, Einsteinweg 55, NL-2333 CC Leiden, Netherlands