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      Pressure and stretch differentially affect proliferation of renal proximal tubular cells

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          Abstract

          Renal obstruction is frequently found in adults and children. Mechanical stimuli, including pressure and stretch in the obstructed kidney, contribute to damage; animal models of obstruction are characterized by increased cellular proliferation. We were interested in the direct effects of pressure and stretch on renal tubular cell proliferation. Human HKC‐8 or rat NRK‐52E proximal tubule cells were subjected to either pressure [0, 60 or 90 mmHg] or static stretch [0 or 20%] for 24 or 48 h. Cell proliferation was measured by cell counting, cell cycle analyzed by flow cytometry, and PCNA and Skp2 expression were determined by qPCR or western blot. Blood gases were determined in an iSTAT system. Proliferation was also assessed in vivo after 24 h of ureteral obstruction. There was a significant increase in HKC‐8 cell number after 48 h of exposure to either 60 or 90 mmHg pressure. Western blot and qPCR confirmed increased expression of PCNA and Skp2 in pressurized cells. Cell cycle measurements demonstrated an increase in HKC‐8 in S phase. Mechanical stretching increased PCNA protein expression in HKC‐8 cells after 48 h while no effect was observed on Skp2 and cell cycle measurements. Increased PCNA expression was found at 24 h after ureteral obstruction. We demonstrate direct transduction of pressure into a proliferative response in HKC‐8 and NRK‐52E cells, measured by cell number, PCNA and Skp2 expression and increase in cells in S phase, whereas stretch had a less robust effect on proliferation.

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          Most cited references37

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          Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals.

          We cloned p27Kip1, a cyclin-dependent kinase inhibitor implicated in G1 phase arrest by TGF beta and cell-cell contact. p27Kip1 associates with cyclin E-Cdk2 complexes in vivo and in vitro, prevents their activation, and inhibits previously activated complexes, and p27Kip1 overexpression obstructs cell entry into S phase. p27Kip1 potently inhibits Rb phosphorylation by cyclin E-Cdk2, cyclin A-Cdk2, and cyclin D2-Cdk4. p27Kip1 is highly conserved and broadly expressed in human tissues, and its mRNA levels are similar in proliferating and quiescent cells. p27Kip1 has a region of sequence similarity to p21Cip1/WAF1, the Cdk inhibitor whose transcription is stimulated by p53. A p27Kip1 peptide corresponding to this region retains Cdk inhibitory activity. We suggest that cell contact, TGF beta, and p53 all restrain cell proliferation through related Cdk inhibitors.
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            Stain-Free technology as a normalization tool in Western blot analysis.

            Western blots are used to specifically measure the relative quantities of proteins of interest in complex biological samples. Quantitative measurements can be subject to error due to process inconsistencies such as uneven protein transfer to the membrane. These non-sample-related variations need to be compensated for by an approach known as normalization. Two approaches to data normalization are commonly employed: housekeeping protein (HKP) normalization and total protein normalization (TPN). In this study, we evaluated the performance of Stain-Free technology as a novel TPN tool for Western blotting experiments in comparison with glyceraldehyde-3-phosphate dehydrogenase (GAPDH) as a representative of the HKP normalization strategy. The target protein (TP) used for this study was MCM7, a DNA licensing replication factor, which was shown previously to be down-regulated by 20% in irradiated lymphoblastoid cell lines (LCLs). We studied the regulation of MCM7 with a multiplex Western blotting approach based on fluorescently labeled secondary antibodies and found that Stain-Free technology appears to be more reliable, more robust, and more sensitive to small effects of protein regulation when compared with HKP normalization with GAPDH. Stain-Free technology offers the additional advantages of providing checkpoints throughout the Western blotting process by allowing rapid visualization of gel separation and protein transfer. Copyright © 2012 Elsevier Inc. All rights reserved.
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              Role of the SCFSkp2 ubiquitin ligase in the degradation of p21Cip1 in S phase.

              The cyclin-dependent kinase inhibitor p21Cip1 has important roles in the control of cell proliferation, differentiation, senescence, and apoptosis. It has been observed that p21 is a highly unstable protein, but the mechanisms of its degradation remained unknown. We show here that p21 is a good substrate for an SCF (Skp1-Cullin1-F-box protein) ubiquitin ligase complex, which contains the F-box protein Skp2 (S phase kinase-associated protein 2) and the accessory protein Cks1 (cyclin kinase subunit 1). A similar ubiquitin ligase complex has been previously shown to be involved in the degradation of a related cyclin-dependent kinase inhibitor, p27Kip1. The levels of Skp2 oscillate in the cell cycle, reaching a maximum in S phase. The ubiquitylation of p21 in vitro required the supplementation of all components of the SCF complex as well as of Cks1 and Cdk2-cyclin E. The protein kinase Cdk2-cyclin E acts both by the phosphorylation of p21 on Ser-130 and by the formation of a complex with p21, which is required for its presentation to the ubiquitin ligase. As opposed to the case of p27, the phosphorylation of p21 stimulates its ubiquitylation but is not absolutely required for this process. Levels of p21 are higher in Skp2-/- mouse embryo fibroblasts than in wild-type fibroblasts in the S phase, and the rates of the degradation of p21 are slower in cells that lack Skp2. It is suggested that SCFSkp2 participates in the degradation of p21 in the S phase.
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                Author and article information

                Contributors
                dfelsen@med.cornell.edu
                Journal
                Physiol Rep
                Physiol Rep
                10.1002/(ISSN)2051-817X
                PHY2
                physreports
                Physiological Reports
                John Wiley and Sons Inc. (Hoboken )
                2051-817X
                14 September 2017
                September 2017
                : 5
                : 17 ( doiID: 10.1002/phy2.2017.5.issue-17 )
                : e13346
                Affiliations
                [ 1 ] Department of Urology Institute for Pediatric Urology Komansky Center for Children's Health Weill Cornell Medicine New York New York
                [ 2 ] Center for Clinical and Translational Science Rockefeller University New York New York
                [ 3 ] Department of Clinical Medicine Aarhus University Aarhus C. Denmark
                Author notes
                [*] [* ] Correspondence

                Diane Felsen, Department of Urology, Institute for Pediatric Urology Research Lab, Weill Cornell Medical College, Box 94, 1300 York Avenue, New York, NY 10065.

                Tel: 212 746 5796; 917 657 3610

                Fax: 212 746 8065

                E‐mail: dfelsen@ 123456med.cornell.edu

                Article
                PHY213346
                10.14814/phy2.13346
                5599855
                28904080
                049fcd9e-d03a-44bb-b03b-faf9e1edbb50
                © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society.

                This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 12 January 2017
                : 14 June 2017
                Page count
                Figures: 6, Tables: 3, Pages: 13, Words: 7590
                Funding
                Funded by: Frederick J. and Theresa Dow Wallace Fund of the New York Community Trust
                Funded by: Grateful Foundation and the Simon and Eve Colin Foundation
                Funded by: Lundbeck Foundation
                Funded by: Karen Elise Jensen Foundation
                Funded by: National Center for Advancing Translational Sciences
                Award ID: UL1TR000043
                Funded by: APS STEP‐UP programs
                Categories
                Renal Physiology
                Cellular Physiology
                Blood Pressure
                Original Research
                Original Research
                Custom metadata
                2.0
                phy213346
                September 2017
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.1.9 mode:remove_FC converted:15.09.2017

                cell cycle,pressure,proliferation,renal tubules,skp2,stretch
                cell cycle, pressure, proliferation, renal tubules, skp2, stretch

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