Sökning: WFRF:(Svensson Jenny) > A CRISP(e)R view on...
Fältnamn | Indikatorer | Metadata |
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000 | 03955naa a2200673 4500 | |
001 | oai:gup.ub.gu.se/273859 | |
003 | SwePub | |
008 | 240528s2018 | |||||||||||000 ||eng| | |
009 | oai:prod.swepub.kib.ki.se:139588410 | |
024 | 7 | a https://gup.ub.gu.se/publication/2738592 URI |
024 | 7 | a https://doi.org/10.1016/j.kint.2018.05.0032 DOI |
024 | 7 | a http://kipublications.ki.se/Default.aspx?queryparsed=id:1395884102 URI |
040 | a (SwePub)gud (SwePub)ki | |
041 | a eng | |
042 | 9 SwePub | |
072 | 7 | a ref2 swepub-contenttype |
072 | 7 | a art2 swepub-publicationtype |
100 | 1 | a Borestrom, C.4 aut |
245 | 1 0 | a A CRISP(e)R view on kidney organoids allows generation of an induced pluripotent stem cell-derived kidney model for drug discovery |
264 | 1 | b Elsevier BV,c 2018 |
520 | a Development of physiologically relevant cellular models with strong translatability to human pathophysiology is critical for identification and validation of novel therapeutic targets. Herein we describe a detailed protocol for generation of an advanced 3-dimensional kidney cellular model using induced pluripotent stem cells, where differentiation and maturation of kidney progenitors and podocytes can be monitored in live cells due to CRISPR/Cas9-mediated fluorescent tagging of kidney lineage markers (SIX2 and NPHS1). Utilizing these cell lines, we have refined the previously published procedures to generate a new, higher throughput protocol suitable for drug discovery. Using paraffin-embedded sectioning and whole-mount immunostaining, we demonstrated that organoids grown in suspension culture express key markers of kidney biology (WT1, ECAD, LTL, nephrin) and vasculature (CD31) within renal cortical structures with microvilli, tight junctions and podocyte foot processes visualized by electron microscopy. Additionally, the organoids resemble the adult kidney transcriptomics profile, thereby strengthening the translatability of our in vitro model. Thus, development of human nephron-like structures in vitro fills a major gap in our ability to assess the effect of potential treatment on key kidney structures, opening up a wide range of possibilities to improve clinical translation. | |
650 | 7 | a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicin0 (SwePub)3022 hsv//swe |
650 | 7 | a MEDICAL AND HEALTH SCIENCESx Clinical Medicine0 (SwePub)3022 hsv//eng |
653 | a glomerulus | |
653 | a kidney development | |
653 | a podocyte | |
653 | a proximal tubule | |
653 | a stem cell | |
653 | a rna-seq | |
653 | a epithelial-cells | |
653 | a podocytes | |
653 | a specificity | |
653 | a injury | |
653 | a cas9 | |
653 | a differentiation | |
653 | a proteinuria | |
653 | a mechanisms | |
653 | a crosstalk | |
653 | a Urology & Nephrology | |
700 | 1 | a Jonebring, A.4 aut |
700 | 1 | a Guo, J.4 aut |
700 | 1 | a Palmgren, H.4 aut |
700 | 1 | a Cederblad, L.4 aut |
700 | 1 | a Forslow, A.4 aut |
700 | 1 | a Svensson, A.4 aut |
700 | 1 | a Soderberg, M.4 aut |
700 | 1 | a Reznichenko, A.4 aut |
700 | 1 | a Nyström, Jenny,d 1972u Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi,Institute of Neuroscience and Physiology4 aut0 (Swepub:gu)xnysje |
700 | 1 | a Patrakka, J.u Karolinska Institutet4 aut |
700 | 1 | a Hicks, R.4 aut |
700 | 1 | a Maresca, M.4 aut |
700 | 1 | a Valastro, B.4 aut |
700 | 1 | a Collen, A.4 aut |
710 | 2 | a Göteborgs universitetb Institutionen för neurovetenskap och fysiologi4 org |
773 | 0 | t Kidney Internationald : Elsevier BVg 94:6, s. 1099-1110q 94:6<1099-1110x 0085-2538x 1523-1755 |
856 | 4 | u http://www.kidney-international.org/article/S0085253818303569/pdf |
856 | 4 8 | u https://gup.ub.gu.se/publication/273859 |
856 | 4 8 | u https://doi.org/10.1016/j.kint.2018.05.003 |
856 | 4 8 | u http://kipublications.ki.se/Default.aspx?queryparsed=id:139588410 |
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