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      Notch signaling in the collecting duct regulates renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction in mice

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          Abstract

          Background/Aims

          Mind bomb-1 ( Mib1) encodes an E3 ubiquitin ligase, which is required for the initiation of Notch signaling. Recently, it was demonstrated that the renal collecting duct plays an important role in renal fibrosis. Here, we investigated the role of Notch signaling in renal fibrosis using conditional knockout mice with the specific ablation of Mib1 in renal collecting duct principal cells.

          Methods

          Mib1-floxed mice ( Mib1 f/f ) were crossed with aquaporin 2 ( AQP2)-Cre mice in order to generate principal cell-specific Mib1 knockout mice ( Mib1 f/f : AQP2-Cre +). Unilateral ureteral obstruction (UUO) was performed, and mice were sacrificed 7 days after UUO.

          Results

          After performing the UUO, renal tubulointerstitial fibrosis and the expression of transforming growth factor β were markedly enhanced in the obstructed kidneys of Mib1 f/f mice compared with the sham-operated kidney of Mib1 f/f mice. These changes were shown to be even more pronounced in the obstructed kidneys of Mib1 f/f : AQP2-Cre + mice than in those of the Mib1 f/f mice . Furthermore, the number of TUNNEL-positive cells in renal collecting duct was higher in the obstructed kidneys of Mib1 f/f : AQP2-Cre + mice than in the kidneys of Mib1 f/f mice.

          Conclusions

          Notch signaling in the renal collecting duct plays an important role in the regulation of renal tubulointerstitial fibrosis and apoptosis after UUO.

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          Most cited references22

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          The canonical Notch signaling pathway: unfolding the activation mechanism.

          Notch signaling regulates many aspects of metazoan development and tissue renewal. Accordingly, the misregulation or loss of Notch signaling underlies a wide range of human disorders, from developmental syndromes to adult-onset diseases and cancer. Notch signaling is remarkably robust in most tissues even though each Notch molecule is irreversibly activated by proteolysis and signals only once without amplification by secondary messenger cascades. In this Review, we highlight recent studies in Notch signaling that reveal new molecular details about the regulation of ligand-mediated receptor activation, receptor proteolysis, and target selection.
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            Tubulointerstitial changes as a major determinant in the progression of renal damage.

            Tubulointerstitial injury is an invariant finding in the chronically diseased kidney, irrespective of the type of disease or the compartment in which the disease originates. Such histologic changes are functionally significant in that scores for such damage, rather than glomerular injury, correlate with decline of renal function. This review summarizes (1) clinical evidence attesting to tubulointerstitial changes as an index of functional impairment, (2) mechanisms by which tubulointerstitial injury impairs renal function, and (3) interactions of pathologic processes in the vascular, glomerular, tubular, and interstitial compartments that culminate in tubulointerstitial injury. This report concludes with a review of interstitial fibrosis, a pathologic process regarded as an irreversible outcome from tubulointerstitial injury.
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              Mind bomb is a ubiquitin ligase that is essential for efficient activation of Notch signaling by Delta.

              Lateral inhibition, mediated by Notch signaling, leads to the selection of cells that are permitted to become neurons within domains defined by proneural gene expression. Reduced lateral inhibition in zebrafish mib mutant embryos permits too many neural progenitors to differentiate as neurons. Positional cloning of mib revealed that it is a gene in the Notch pathway that encodes a RING ubiquitin ligase. Mib interacts with the intracellular domain of Delta to promote its ubiquitylation and internalization. Cell transplantation studies suggest that mib function is essential in the signaling cell for efficient activation of Notch in neighboring cells. These observations support a model for Notch activation where the Delta-Notch interaction is followed by endocytosis of Delta and transendocytosis of the Notch extracellular domain by the signaling cell. This facilitates intramembranous cleavage of the remaining Notch receptor, release of the Notch intracellular fragment, and activation of target genes in neighboring cells.
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                Author and article information

                Journal
                Korean J Intern Med
                Korean J. Intern. Med
                KJIM
                The Korean Journal of Internal Medicine
                The Korean Association of Internal Medicine
                1226-3303
                2005-6648
                July 2018
                26 May 2017
                : 33
                : 4
                : 774-782
                Affiliations
                [1 ]Department of Anatomy and Cell Death Disease Research Center, College of Medicine, The Catholic University of Korea, Seoul, Korea
                [2 ]Institute of Clinical Medicine Research of Bucheon St. Mary’s Hospital, Bucheon, Korea
                [3 ]Division of Nephrology, Department of Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea
                [4 ]Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea
                Author notes
                Correspondence to Jin Kim, M.D. Department of Anatomy and Cell Death Disease Research Center, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Korea Tel: +82-2-2258-7258 Fax: +82-2-2536-3110 E-mail: jinkim@ 123456catholic.ac.kr
                Article
                kjim-2016-230
                10.3904/kjim.2016.230
                6030409
                28602064
                313cc48f-081f-44e9-a35a-a88112c3cee0
                Copyright © 2018 The Korean Association of Internal Medicine

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 July 2016
                : 22 September 2016
                : 24 September 2016
                Categories
                Original Article
                Nephrology

                Internal medicine
                mib1,notch,renal fibrosis,kidney collecting duct,ureteral obstruction
                Internal medicine
                mib1, notch, renal fibrosis, kidney collecting duct, ureteral obstruction

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