دورية أكاديمية

Modelling ciliopathy phenotypes in human tissues derived from pluripotent stem cells with genetically ablated cilia.

التفاصيل البيبلوغرافية
العنوان: Modelling ciliopathy phenotypes in human tissues derived from pluripotent stem cells with genetically ablated cilia.
المؤلفون: Cruz, Nelly M, Reddy, Raghava, McFaline-Figueroa, José L, Tran, Christine, Fu, Hongxia, Freedman, Benjamin S
المصدر: Nat Biomed Eng ; ISSN:2157-846X ; Volume:6 ; Issue:4
بيانات النشر: Nature Publishing Group
سنة النشر: 2022
المجموعة: PubMed Central (PMC)
الوصف: The functions of cilia-antenna-like organelles associated with a spectrum of disease states-are poorly understood, particularly in human cells. Here we show that human pluripotent stem cells (hPSCs) edited via CRISPR to knock out the kinesin-2 subunits KIF3A or KIF3B can be used to model ciliopathy phenotypes and to reveal ciliary functions at the tissue scale. KIF3A-/- and KIF3B-/- hPSCs lacked cilia, yet remained robustly self-renewing and pluripotent. Tissues and organoids derived from these hPSCs displayed phenotypes that recapitulated defective neurogenesis and nephrogenesis, polycystic kidney disease (PKD) and other features of the ciliopathy spectrum. We also show that human cilia mediate a critical switch in hedgehog signalling during organoid differentiation, and that they constitutively release extracellular vesicles containing signalling molecules associated with ciliopathy phenotypes. The capacity of KIF3A-/- and KIF3B-/- hPSCs to reveal endogenous mechanisms underlying complex ciliary phenotypes may facilitate the discovery of candidate therapeutics.
نوع الوثيقة: article in journal/newspaper
اللغة: English
العلاقة: https://doi.org/10.1038/s41551-022-00880-8Test; https://pubmed.ncbi.nlm.nih.gov/35478224Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228023Test/
DOI: 10.1038/s41551-022-00880-8
الإتاحة: https://doi.org/10.1038/s41551-022-00880-8Test
https://pubmed.ncbi.nlm.nih.gov/35478224Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9228023Test/
حقوق: © 2022. The Author(s), under exclusive licence to Springer Nature Limited.
رقم الانضمام: edsbas.477C815C
قاعدة البيانات: BASE