keyword
https://read.qxmd.com/read/38163671/role-of-the-ste20-like-kinase-slk-in-podocyte-adhesion
#1
JOURNAL ARTICLE
Andrey V Cybulsky, Joan Papillon, Craig Bryan, José R Navarro-Betancourt, Luc A Sabourin
SLK controls the cytoskeleton, cell adhesion, and migration. Podocyte-specific deletion of SLK in mice leads to podocyte injury as mice age and exacerbates injury in experimental focal segment glomerulosclerosis (FSGS; adriamycin nephrosis). We hypothesized that adhesion proteins may be substrates of SLK. In adriamycin nephrosis, podocyte ultrastructural injury was exaggerated by SLK deletion. Analysis of a protein kinase phosphorylation site dataset showed that podocyte adhesion proteins-paxillin, vinculin, and talin-1 may be potential SLK substrates...
January 2024: Physiological Reports
https://read.qxmd.com/read/36060790/integrin-%C3%AE-3-negative-podocytes-a-gene-expression-study
#2
JOURNAL ARTICLE
L H Frommherz, S B Sayar, Y Wang, L K Trefzer, Y He, J Leppert, P Eßer, C Has
Integrin α3β1 is a cell adhesion receptor widely expressed in epithelial cells. Pathogenic variants in the gene encoding the integrin α3 subunit ITGA3 lead to a syndrome including interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa (ILNEB). Renal involvement mainly consists of glomerular disease caused by loss of adhesion between podocytes and the glomerular basement membrane. The aim of this study was to characterize the impact of loss of integrin α3 on human podocytes. ITGA3 was stably knocked-out in the human podocyte cell line AB8/13, designated as PodoA3- , and in human proximal tubule epithelial cell line HK2 using the targeted genome editing technique CRISPR/Cas9...
December 2022: Matrix biology plus
https://read.qxmd.com/read/31853790/assessment-of-increased-glomerular-permeability-associated-with-recurrent-focal-segmental-glomerulosclerosis-using-an-in-vitro-model-of-the-glomerular-filtration-barrier
#3
JOURNAL ARTICLE
Min Li, Carlo Maria Alfieri, William Morello, Francesco Cellesi, Silvia Armelloni, Deborah Mattinzoli, Giovanni Montini, Piergiorgio Messa
The presence of circulating permeability factors (cPFs) has been hypothesized to be associated with recurrence of focal segmental glomerulosclerosis (rFSGS) in renal allografts. The available methods to detect cPFs are complex, not easily repeatable and inappropriate to represent the anatomical characteristics of the three-layer glomerular filtration barrier (GFB). Here we describe a novel method which measures the permeability to bovine serum albumin (BSA) through a three-layer device (3LD). The 3 layers comprise: (1) conditionally immortalized human podocytes (HCiPodo), (2) collagen type IV coated porous membrane and (3) human glomerular endothelial cells (HCiGEnC)...
August 2020: Journal of Nephrology
https://read.qxmd.com/read/31816967/substrate-stiffness-modulates-renal-progenitor-cell-properties-via-a-rock-mediated-mechanotransduction-mechanism
#4
JOURNAL ARTICLE
Maria Elena Melica, Gilda La Regina, Matteo Parri, Anna Julie Peired, Paola Romagnani, Laura Lasagni
Stem cell (SC)-based tissue engineering and regenerative medicine (RM) approaches may provide alternative therapeutic strategies for the rising number of patients suffering from chronic kidney disease. Embryonic SCs and inducible pluripotent SCs are the most frequently used cell types, but autologous patient-derived renal SCs, such as human CD133+CD24+ renal progenitor cells (RPCs), represent a preferable option. RPCs are of interest also for the RM approaches based on the pharmacological encouragement of in situ regeneration by endogenous SCs...
December 3, 2019: Cells
https://read.qxmd.com/read/30104322/induced-pluripotent-stem-cell-derived-podocyte-like-cells-as-models-for-assessing-mechanisms-underlying-heritable-disease-phenotype-initial-studies-using-two-alport-syndrome-patient-lines-indicate-impaired-potassium-channel-activity
#5
JOURNAL ARTICLE
John M Haynes, James N Selby, Teresa H Vandekolk, Isaiah P L Abad, Joan K Ho, Wai-Ling Lieuw, Katie Leach, Judith Savige, Sheetal Saini, Craig L Fisher, Sharon D Ricardo
Renal podocyte survival depends upon the dynamic regulation of a complex cell architecture that links the glomerular basement membrane to integrins, ion channels, and receptors. Alport syndrome is a heritable chronic kidney disease where mutations in α 3, α 4, or α 5 collagen genes promote podocyte death. In rodent models of renal failure, activation of the calcium-sensing receptor (CaSR) can protect podocytes from stress-related death. In this study, we assessed CaSR function in podocyte-like cells derived from induced-pluripotent stem cells from two patients with Alport Syndrome (AS1 & AS2) and a renal disease free individual [normal human mesangial cell (NHMC)], as well as a human immortalized podocyte-like (HIP) cell line...
November 2018: Journal of Pharmacology and Experimental Therapeutics
https://read.qxmd.com/read/29572404/similar-biophysical-abnormalities-in-glomeruli-and-podocytes-from-two-distinct-models
#6
JOURNAL ARTICLE
Addie E Embry, Zhenan Liu, Joel M Henderson, F Jefferson Byfield, Liping Liu, Joonho Yoon, Zhenzhen Wu, Katrina Cruz, Sara Moradi, C Barton Gillombardo, Rihanna Z Hussain, Richard Doelger, Olaf Stuve, Audrey N Chang, Paul A Janmey, Leslie A Bruggeman, R Tyler Miller
Background FSGS is a pattern of podocyte injury that leads to loss of glomerular function. Podocytes support other podocytes and glomerular capillary structure, oppose hemodynamic forces, form the slit diaphragm, and have mechanical properties that permit these functions. However, the biophysical characteristics of glomeruli and podocytes in disease remain unclear. Methods Using microindentation, atomic force microscopy, immunofluorescence microscopy, quantitative RT-PCR, and a three-dimensional collagen gel contraction assay, we studied the biophysical and structural properties of glomeruli and podocytes in chronic (Tg26 mice [HIV protein expression]) and acute (protamine administration [cytoskeletal rearrangement]) models of podocyte injury...
May 2018: Journal of the American Society of Nephrology: JASN
https://read.qxmd.com/read/27882344/slit2-robo2-signaling-pathway-inhibits-nonmuscle-myosin-iia-activity-and-destabilizes-kidney-podocyte-adhesion
#7
JOURNAL ARTICLE
Xueping Fan, Hongying Yang, Sudhir Kumar, Kathleen E Tumelty, Anna Pisarek-Horowitz, Hila Milo Rasouly, Richa Sharma, Stefanie Chan, Edyta Tyminski, Michael Shamashkin, Mostafa Belghasem, Joel M Henderson, Anthony J Coyle, David J Salant, Stephen P Berasi, Weining Lu
The repulsive guidance cue SLIT2 and its receptor ROBO2 are required for kidney development and podocyte foot process structure, but the SLIT2/ROBO2 signaling mechanism regulating podocyte function is not known. Here we report that a potentially novel signaling pathway consisting of SLIT/ROBO Rho GTPase activating protein 1 (SRGAP1) and nonmuscle myosin IIA (NMIIA) regulates podocyte adhesion downstream of ROBO2. We found that the myosin II regulatory light chain (MRLC), a subunit of NMIIA, interacts directly with SRGAP1 and forms a complex with ROBO2/SRGAP1/NMIIA in the presence of SLIT2...
November 17, 2016: JCI Insight
https://read.qxmd.com/read/23988887/tenc1-deficient-mice-develop-glomerular-disease-in-a-strain-specific-manner
#8
JOURNAL ARTICLE
Kozue Uchio-Yamada, Kyoko Sawada, Kotaro Tamura, Sumie Katayama, Youko Monobe, Yoshie Yamamoto, Atsuo Ogura, Noboru Manabe
BACKGROUND/AIMS: Tenc1 (also known as tensin2) is an integrin-associated focal adhesion molecule that is broadly expressed in mouse tissues including the liver, muscle, heart and kidney. A mouse strain carrying mutated Tenc1, the ICR-derived glomerulonephritis (ICGN) strain, develops severe nephrotic syndrome. METHODS: To elucidate the function of Tenc1 in the kidney, Tenc1(ICGN) was introduced into 2 genetic backgrounds, i.e. DBA/2J (D2) and C57BL/6J (B6), strains that are respectively susceptible and resistant to chronic kidney disease...
2013: Nephron. Experimental Nephrology
https://read.qxmd.com/read/22126861/clinical-significance-of-fibroblast-specific-protein-1-expression-on-podocytes-in-patients-with-focal-segmental-glomerulosclerosis
#9
COMPARATIVE STUDY
Ken-Ichi Samejima, Kimihiko Nakatani, Daisuke Suzuki, Osamu Asai, Hirokazu Sakan, Shuhei Yoshimoto, Yukinari Yamaguchi, Masaru Matsui, Yasuhiro Akai, Masao Toyoda, Masayuki Iwano, Yoshihiko Saito
BACKGROUNDS/AIMS: We previously reported that fibroblast-specific protein 1 (FSP1) is a marker of epithelial-mesenchymal transition (EMT) in tubulointerstitial fibrosis. The EMT-like changes observed in podocytes are reportedly associated with podocyte detachment which may cause focal glomerulosclerosis. METHODS: In cross-sectional studies, we analyzed podocyte expression of FSP1 immunohistochemically using renal biopsy specimens from 31 patients with focal segmental glomerulosclerosis (FSGS) and 39 patients with minimal change disease (MCD)...
2012: Nephron. Clinical Practice
https://read.qxmd.com/read/21814837/connective-tissue-growth-factor-modulates-podocyte-actin-cytoskeleton-and-extracellular-matrix-synthesis-and-is-induced-in-podocytes-upon-injury
#10
JOURNAL ARTICLE
Rudolf Fuchshofer, Sabrina Ullmann, Ludwig F Zeilbeck, Matti Baumann, Benjamin Junglas, Ernst R Tamm
Structural changes of podocytes and retraction of their foot processes are a critical factor in the pathogenesis of minimal change nephritis and glomerulosclerosis. Here we tested, if connective tissue growth factor (CTGF) is involved in podocyte injury during acute and chronic puromycin aminonucleoside nephrosis (PAN) as animal models of minimal change nephritis, and focal segmental glomerulosclerosis, respectively. Rats were treated once (acute PAN) or for 13 weeks (chronic PAN). In both experimental conditions, CTGF and its mRNA were found to be highly upregulated in podocytes...
September 2011: Histochemistry and Cell Biology
https://read.qxmd.com/read/21734098/advanced-glycation-end-products-inhibit-adhesion-ability-of-differentiated-podocytes-in-a-neuropilin-1-dependent-manner
#11
JOURNAL ARTICLE
Tzvetanka Bondeva, Stefanie Wojciech, Gunter Wolf
Podocyte injury can occur by a number of stimuli. Maintaining of an intact podocyte structure is essential for glomerular filtration; therefore, podocyte damage severely impairs renal function. Recently, we have reported that addition of glycated BSA [advanced glycation end products (AGE)-BSA] to differentiated murine podocytes inhibited neuropilin-1 (NRP1) expression and dramatically influenced podocyte migration ability (Bondeva T, Ruster C, Franke S, Hammerschmid E, Klagsbrun M, Cohen CD, Wolf G. Kidney Int 75: 605-616, 2009; Bondeva T, Wolf G...
October 2011: American Journal of Physiology. Renal Physiology
https://read.qxmd.com/read/21160460/focal-segmental-glomerulosclerosis-plays-a-major-role-in-the-progression-of-iga-nephropathy-i-immunohistochemical-studies
#12
JOURNAL ARTICLE
Gary S Hill, Khalil El Karoui, Alexandre Karras, Chantal Mandet, Jean-Paul Duong Van Huyen, Dominique Nochy, Patrick Bruneval
IgA nephropathy (IgAN) often shows lesions morphologically identical with those of focal segmental glomerulosclerosis (FSGS). In order to determine the possible role of FSGS in IgAN lesions, we measured glomerular capsular adhesions, often the first step toward FSGS, in biopsies from 127 patients with IgAN, 100 with lupus nephritis, and 26 with primary FSGS. Capsular adhesions with no lesions in the underlying tuft, consistent with podocyte abnormality or loss, were found regularly in FSGS and IgAN, but infrequently in lupus...
March 2011: Kidney International
https://read.qxmd.com/read/21159733/endoplasmic-reticulum-stress-in-glomerular-epithelial-cell-injury
#13
JOURNAL ARTICLE
Andrey V Cybulsky, Tomoko Takano, Joan Papillon, Thomas M Kitzler, Krikor Bijian
Focal segmental glomerulosclerosis (FSGS) may be associated with glomerular epithelial cell (GEC; podocyte) apoptosis due to acquired injury or mutations in specific podocyte proteins. This study addresses mediation of GEC injury, focusing on endoplasmic reticulum (ER) stress. We studied signaling in cultured GECs in the presence or absence of the extracellular matrix (ECM). Adhesion to collagen supports cell survival, but adhesion to plastic (loss of contact with ECM) leads to apoptosis. Compared with collagen-adherent cells, GECs on plastic showed increased protein misfolding in the ER, and an adaptive-protective ER stress response, including increased expression of ER chaperones, increased phosphorylation of eukaryotic translation initiation factor-2α (eIF2α), and a reduction in protein synthesis...
September 2011: American Journal of Physiology. Renal Physiology
https://read.qxmd.com/read/18855004/myocilin-promotes-substrate-adhesion-spreading-and-formation-of-focal-contacts-in-podocytes-and-mesangial-cells
#14
JOURNAL ARTICLE
Andreas Goldwich, Michael Scholz, Ernst R Tamm
Myocilin, a secreted glycoprotein of the olfactomedin family, is constitutively expressed in podocytes of the rat kidney and induced in mesangial cells during mesangioproliferative glomerulonephritis. As myocilin has been found to be associated with fibrillar components of the extracellular matrix, and adhesive properties have been shown for other members of the olfactomedin family, we hypothesized that myocilin might play a role in cell-matrix interactions in the glomerulus. To elucidate functional properties of myocilin, recombinant myocilin was expressed in 293 EBNA cells and purified by Ni-chelate and heparin chromatography...
February 2009: Histochemistry and Cell Biology
https://read.qxmd.com/read/16837921/fsgs-associated-alpha-actinin-4-k256e-impairs-cytoskeletal-dynamics-in-podocytes
#15
COMPARATIVE STUDY
J-L R Michaud, K M Chaisson, R J Parks, C R J Kennedy
Mutations in the ACTN4 gene, encoding the actin crosslinking protein alpha-actinin-4, are associated with a familial form of focal segmental glomerulosclerosis (FSGS). Mice with podocyte-specific expression of K256E alpha-actinin-4 develop foot process effacement and glomerulosclerosis, highlighting the importance of the cytoskeleton in podocyte structure and function. K256E alpha-actinin-4 exhibits increased affinity for F-actin. However, the downstream effects of this aberrant binding on podocyte dynamics remain unclear...
September 2006: Kidney International
https://read.qxmd.com/read/16014575/actin-cytoskeleton-regulates-extracellular-matrix-dependent-survival-signals-in-glomerular-epithelial-cells
#16
JOURNAL ARTICLE
Krikor Bijian, Tomoko Takano, Joan Papillon, Ludmilla Le Berre, Jean-Louis Michaud, Chris R J Kennedy, Andrey V Cybulsky
Adhesion of rat glomerular epithelial cells (GEC) to collagen activates focal adhesion kinase (FAK) and the Ras-extracellular signal-regulated kinase (ERK) pathway and supports survival (prevents apoptosis). The present study addresses the relationship between actin organization and the survival phenotype. Parental GEC (adherent to collagen) and GEC stably transfected with constitutively active mutants of mitogen-activated protein kinase kinase (R4F-MEK) or FAK (CD2-FAK) (on plastic) showed ERK activation, low levels of apoptosis, and a cortical distribution of F-actin...
December 2005: American Journal of Physiology. Renal Physiology
https://read.qxmd.com/read/15200417/ddr1-deficient-mice-show-localized-subepithelial-gbm-thickening-with-focal-loss-of-slit-diaphragms-and-proteinuria
#17
JOURNAL ARTICLE
Oliver Gross, Bogdan Beirowski, Scott J Harvey, Catherine McFadden, Dilys Chen, Stephanie Tam, Paul S Thorner, Neil Smyth, Klaus Addicks, Wilhelm Bloch, Yoshifumi Ninomiya, Yoshikazu Sado, Manfred Weber, Wolfgang F Vogel
BACKGROUND: Type IV collagen in basement membranes is a ligand for the receptor tyrosine kinase discoidin domain receptor 1 (DDR1). DDR1 is expressed in renal cells and regulates cell adhesion and proliferation ex vivo. The interaction between type IV collagen and cell surface receptors is believed important for normal renal function as well as significant in chronic renal diseases and we therefore analyzed mice with a targeted deletion of DDR1. METHODS: Homozygous DDR1 knockout mice were compared to heterozygous and wild-type animals...
July 2004: Kidney International
https://read.qxmd.com/read/15034095/the-parietal-epithelial-cell-a-key-player-in-the-pathogenesis-of-focal-segmental-glomerulosclerosis-in-thy-1-1-transgenic-mice
#18
JOURNAL ARTICLE
Bart Smeets, Nathalie A J M Te Loeke, Henry B P M Dijkman, Mark L M Steenbergen, Joost F M Lensen, Mark P V Begieneman, Toin H van Kuppevelt, Jack F M Wetzels, Eric J Steenbergen
Focal segmental glomerulosclerosis (FSGS) is a hallmark of progressive renal disease. Podocyte injury and loss have been proposed as the critical events that lead to FSGS. In the present study, the authors have examined the development of FSGS in Thy-1.1 transgenic (tg) mice, with emphasis on the podocyte and parietal epithelial cell (PEC). Thy-1.1 tg mice express the Thy-1.1 antigen on podocytes. Injection of anti-Thy-1.1 mAb induces an acute albuminuria and development of FSGS lesions that resemble human collapsing FSGS...
April 2004: Journal of the American Society of Nephrology: JASN
https://read.qxmd.com/read/12354696/analysis-of-differential-gene-expression-in-stretched-podocytes-osteopontin-enhances-adaptation-of-podocytes-to-mechanical-stress
#19
JOURNAL ARTICLE
Nicole Endlich, Masataka Sunohara, Wilfried Nietfeld, Eryk W Wolski, Daniel Schiwek, Bettina Kränzlin, Norbert Gretz, Wilhelm Kriz, Holger Eickhoff, Karlhans Endlich
Glomerular hypertension is a major determinant advancing progression to end-stage renal failure. Podocytes, which are thought to counteract pressure-mediated capillary expansion, are increasingly challenged in glomerular hypertension. Studies in animal models of glomerular hypertension indicate that glomerulosclerosis develops from adhesions of the glomerular tuft to Bowman's capsule due to progressive podocyte loss. However, the molecular alterations of podocytes in glomerular hypertension are unknown. In this study, we determined the changes in gene expression in podocytes induced by mechanical stress in vitro (cyclic biaxial stretch, 0...
November 2002: FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology
https://read.qxmd.com/read/10620198/early-events-leading-to-renal-injury-in-obese-zucker-fatty-rats-with-type-ii-diabetes
#20
JOURNAL ARTICLE
T M Coimbra, U Janssen, H J Gröne, T Ostendorf, U Kunter, H Schmidt, G Brabant, J Floege
UNLABELLED: Early events leading to renal injury in obese Zucker (fatty) rats with type II diabetes. BACKGROUND: More than half of the new patients admitted to dialysis therapy in some centers are diagnosed with type IIb diabetes, that is, diabetes associated with obesity. This study searched for a common final pathway of renal damage in this progressive renal disease. METHODS: The evolution of biochemical and morphological renal changes was examined in 6- to 60-week-old Zucker rats (fa/fa-rats), a model of obesity associated with type II diabetes...
January 2000: Kidney International
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