1. A reverse genetic screen in the zebrafish identifies crb2b as a regulator of the glomerular filtration barrier
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Ebarasi, Lwaki, He, Liqun, Hultenby, Kjell, Takemoto, Minoru, Betsholtz, Christer, Tryggvason, Karl, and Majumdar, Arindam
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Blood proteins -- Genetic aspects ,Blood proteins -- Analysis ,Blood proteins -- Physiological aspects ,Permeability -- Genetic aspects ,Permeability -- Analysis ,Permeability -- Physiological aspects ,Genetic screening -- Genetic aspects ,Genetic screening -- Analysis ,Genetic screening -- Physiological aspects ,Biological sciences - Abstract
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.ydbio.2009.04.017 Byline: Lwaki Ebarasi (a), Liqun He (b), Kjell Hultenby (c), Minoru Takemoto (d), Christer Betsholtz (b), Karl Tryggvason (a), Arindam Majumdar (a) Keywords: Podocyte; Pronephros; Glomerulus; Glomerular filtration barrier; Nephrin; Zebrafish; Crumbs; Slit diaphragm; Differentiation; Cell polarity Abbreviations: GBM, glomerular basement membrane; dpf, days post fertilization; crb, crumbs Abstract: The glomerular filtration barrier is necessary for the selective passage of low molecular weight waste products and the retention of blood plasma proteins. Damage to the filter results in proteinuria. The filtration barrier is the major pathogenic site in almost all glomerular diseases and its study is therefore of clinical significance. We have taken advantage of the zebrafish pronephros as a system for studying glomerular filtration. In order to identify new regulators of filtration barrier assembly, we have performed a reverse genetic screen in the zebrafish testing a group of genes which are enriched in their expression within the mammalian glomerulus. In this novel screen, we have coupled gene knockdown using morpholinos with a physiological glomerular dye filtration assay to test for selective glomerular permeability in living zebrafish larvae. Screening 20 genes resulted in the identification of ralgps1, rapgef2, rabgef1, and crb2b. The crumbs (crb) genes encode a family of evolutionarily conserved proteins important for apical-basal polarity within epithelia. The crb2b gene is expressed in zebrafish podocytes. Electron microscopic analysis of crb2b morphants reveals a gross disorganization of podocyte foot process architecture and loss of slit diaphragms while overall polarity is maintained. Nephrin, a major component of the slit diaphragm, is apically mis-localized in podocytes from crb2b morphants suggesting that crb2b is required for the proper protein trafficking of Nephrin. This report is the first to show a role for crb function in podocyte differentiation. Furthermore, these results suggest a novel link between epithelial polarization and the maintenance of a functional filtration barrier. Author Affiliation: (a) Division of Matrix Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Scheeles vag 2, Plan 4 B1, SE-171 77 Stockholm, Sweden (b) Laboratory of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, 17177 Stockholm, Sweden (c) Department of Pathology, Karolinska University Hospital/Huddinge, Karolinska Institutet, Stockholm, Sweden (d) Department of Clinical Cell Biology and Medicine, Chiba University Graduate School of Medicine, Chiba, Japan Article History: Received 27 October 2008; Revised 26 March 2009; Accepted 16 April 2009
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- 2009