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  1. Article ; Online: mTOR-Dependent Autophagy Regulates Slit Diaphragm Density in Podocyte-like Drosophila Nephrocytes

    Dominik Spitz / Maria Comas / Lea Gerstner / Séverine Kayser / Martin Helmstädter / Gerd Walz / Tobias Hermle

    Cells, Vol 11, Iss 2103, p

    2022  Volume 2103

    Abstract: Both mTOR signaling and autophagy are important modulators of podocyte homeostasis, regeneration, and aging and have been implicated in glomerular diseases. However, the mechanistic role of these pathways for the glomerular filtration barrier remains ... ...

    Abstract Both mTOR signaling and autophagy are important modulators of podocyte homeostasis, regeneration, and aging and have been implicated in glomerular diseases. However, the mechanistic role of these pathways for the glomerular filtration barrier remains poorly understood. We used Drosophila nephrocytes as an established podocyte model and found that inhibition of mTOR signaling resulted in increased spacing between slit diaphragms. Gain-of-function of mTOR signaling did not affect spacing, suggesting that additional cues limit the maximal slit diaphragm density. Interestingly, both activation and inhibition of mTOR signaling led to decreased nephrocyte function, indicating that a fine balance of signaling activity is needed for proper function. Furthermore, mTOR positively controlled cell size, survival, and the extent of the subcortical actin network. We also showed that basal autophagy in nephrocytes is required for survival and limits the expression of the sns (nephrin) but does not directly affect slit diaphragm formation or endocytic activity. However, using a genetic rescue approach, we demonstrated that excessive, mTOR-dependent autophagy is primarily responsible for slit diaphragm misspacing. In conclusion, we established this invertebrate podocyte model for mechanistic studies on the role of mTOR signaling and autophagy, and we discovered a direct mTOR/autophagy-dependent regulation of the slit diaphragm architecture.
    Keywords nephrocyte ; Drosophila ; podocyte ; mTOR ; autophagy ; slit diaphragm ; Biology (General) ; QH301-705.5
    Subject code 571
    Language English
    Publishing date 2022-07-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Selective endocytosis controls slit diaphragm maintenance and dynamics in Drosophila nephrocytes

    Konrad Lang / Julian Milosavljevic / Helena Heinkele / Mengmeng Chen / Lea Gerstner / Dominik Spitz / Severine Kayser / Martin Helmstädter / Gerd Walz / Michael Köttgen / Andrew Spracklen / John Poulton / Tobias Hermle

    eLife, Vol

    2022  Volume 11

    Abstract: The kidneys generate about 180 l of primary urine per day by filtration of plasma. An essential part of the filtration barrier is the slit diaphragm, a multiprotein complex containing nephrin as major component. Filter dysfunction typically manifests ... ...

    Abstract The kidneys generate about 180 l of primary urine per day by filtration of plasma. An essential part of the filtration barrier is the slit diaphragm, a multiprotein complex containing nephrin as major component. Filter dysfunction typically manifests with proteinuria and mutations in endocytosis regulating genes were discovered as causes of proteinuria. However, it is unclear how endocytosis regulates the slit diaphragm and how the filtration barrier is maintained without either protein leakage or filter clogging. Here, we study nephrin dynamics in podocyte-like nephrocytes of Drosophila and show that selective endocytosis either by dynamin- or flotillin-mediated pathways regulates a stable yet highly dynamic architecture. Short-term manipulation of endocytic functions indicates that dynamin-mediated endocytosis of ectopic nephrin restricts slit diaphragm formation spatially while flotillin-mediated turnover of nephrin within the slit diaphragm is needed to maintain filter permeability by shedding of molecules bound to nephrin in endosomes. Since slit diaphragms cannot be studied in vitro and are poorly accessible in mouse models, this is the first analysis of their dynamics within the slit diaphragm multiprotein complex. Identification of the mechanisms of slit diaphragm maintenance will help to develop novel therapies for proteinuric renal diseases that are frequently limited to symptomatic treatment.
    Keywords nephrocyte ; podocyte ; endocytosis ; nephrin ; proteinuria ; Drosophila ; Medicine ; R ; Science ; Q ; Biology (General) ; QH301-705.5
    Language English
    Publishing date 2022-07-01T00:00:00Z
    Publisher eLife Sciences Publications Ltd
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: V-ATPase/mTOR Signaling Regulates Megalin-Mediated Apical Endocytosis

    Eva Maria Gleixner / Guillaume Canaud / Tobias Hermle / Maria Clara Guida / Oliver Kretz / Martin Helmstädter / Tobias B. Huber / Stefan Eimer / Fabiola Terzi / Matias Simons

    Cell Reports, Vol 8, Iss 1, Pp 10-

    2014  Volume 19

    Abstract: mTOR kinase is a master growth regulator that can be stimulated by multiple signals, including amino acids and the lysosomal small GTPase Rheb. Recent studies have proposed an important role for the V-ATPase in the sensing of amino acids in the lysosomal ...

    Abstract mTOR kinase is a master growth regulator that can be stimulated by multiple signals, including amino acids and the lysosomal small GTPase Rheb. Recent studies have proposed an important role for the V-ATPase in the sensing of amino acids in the lysosomal lumen. Using the Drosophila wing as a model epithelium, we show here that the V-ATPase is required for Rheb-dependent epithelial growth. We further uncover a positive feedback loop for the control of apical protein uptake that depends on V-ATPase/mTOR signaling. This feedback loop includes Rheb-dependent transcriptional regulation of the multiligand receptor Megalin, which itself is required for Rheb-induced endocytosis. In addition, we provide evidence that long-term mTOR inhibition with rapamycin in mice causes reduction of Megalin levels and proteinuria in the proximal tubular epithelium of the kidney. Thus, our findings unravel a homeostatic mechanism that allows epithelial cells to promote protein uptake under normal conditions and to prevent uptake in lysosomal stress conditions.
    Keywords Biology (General) ; QH301-705.5
    Subject code 570
    Language English
    Publishing date 2014-07-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

    Alexander Teumer / Yong Li / Sahar Ghasemi / Bram P. Prins / Matthias Wuttke / Tobias Hermle / Ayush Giri / Karsten B. Sieber / Chengxiang Qiu / Holger Kirsten / Adrienne Tin / Audrey Y. Chu / Nisha Bansal / Mary F. Feitosa / Lihua Wang / Jin-Fang Chai / Massimiliano Cocca / Christian Fuchsberger / Mathias Gorski /
    Anselm Hoppmann / Katrin Horn / Man Li / Jonathan Marten / Damia Noce / Teresa Nutile / Sanaz Sedaghat / Gardar Sveinbjornsson / Bamidele O. Tayo / Peter J. van der Most / Yizhe Xu / Zhi Yu / Lea Gerstner / Johan Ärnlöv / Stephan J. L. Bakker / Daniela Baptista / Mary L. Biggs / Eric Boerwinkle / Hermann Brenner / Ralph Burkhardt / Robert J. Carroll / Miao-Li Chee / Miao-Ling Chee / Mengmeng Chen / Ching-Yu Cheng / James P. Cook / Josef Coresh / Tanguy Corre / John Danesh / Martin H. de Borst / Alessandro De Grandi

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 19

    Abstract: Urinary albumin-to-creatinine ratio (UCAR) is associated with various clinical outcomes such as kidney disease and cardiovascular disease. Here, the authors report genome-wide meta-analysis in over 500,000 individuals and find 68 UACR loci, followed by ... ...

    Abstract Urinary albumin-to-creatinine ratio (UCAR) is associated with various clinical outcomes such as kidney disease and cardiovascular disease. Here, the authors report genome-wide meta-analysis in over 500,000 individuals and find 68 UACR loci, followed by statistical fine-mapping, gene prioritization and experimental validation in flies.
    Keywords Science ; Q
    Language English
    Publishing date 2019-09-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

    Shazia Ashraf / Hiroki Kudo / Jia Rao / Atsuo Kikuchi / Eugen Widmeier / Jennifer A. Lawson / Weizhen Tan / Tobias Hermle / Jillian K. Warejko / Shirlee Shril / Merlin Airik / Tilman Jobst-Schwan / Svjetlana Lovric / Daniela A. Braun / Heon Yung Gee / David Schapiro / Amar J. Majmundar / Carolin E. Sadowski / Werner L. Pabst /
    Ankana Daga / Amelie T. van der Ven / Johanna M. Schmidt / Boon Chuan Low / Anjali Bansal Gupta / Brajendra K. Tripathi / Jenny Wong / Kirk Campbell / Kay Metcalfe / Denny Schanze / Tetsuya Niihori / Hiroshi Kaito / Kandai Nozu / Hiroyasu Tsukaguchi / Ryojiro Tanaka / Kiyoshi Hamahira / Yasuko Kobayashi / Takumi Takizawa / Ryo Funayama / Keiko Nakayama / Yoko Aoki / Naonori Kumagai / Kazumoto Iijima / Henry Fehrenbach / Jameela A. Kari / Sherif El Desoky / Sawsan Jalalah / Radovan Bogdanovic / Nataša Stajić / Hildegard Zappel / Assel Rakhmetova

    Nature Communications, Vol 9, Iss 1, Pp 1-

    2018  Volume 14

    Abstract: Nephrotic syndrome is the second most common chronic kidney disease but there are no targeted treatment strategies available. Here the authors identify mutations of six genes codifying for proteins involved in cytoskeleton remodelling and modulation of ... ...

    Abstract Nephrotic syndrome is the second most common chronic kidney disease but there are no targeted treatment strategies available. Here the authors identify mutations of six genes codifying for proteins involved in cytoskeleton remodelling and modulation of small GTPases in 17 families with nephrotic syndrome.
    Keywords Science ; Q
    Language English
    Publishing date 2018-05-01T00:00:00Z
    Publisher Nature Portfolio
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment

    Shazia Ashraf / Hiroki Kudo / Jia Rao / Atsuo Kikuchi / Eugen Widmeier / Jennifer A. Lawson / Weizhen Tan / Tobias Hermle / Jillian K. Warejko / Shirlee Shril / Merlin Airik / Tilman Jobst-Schwan / Svjetlana Lovric / Daniela A. Braun / Heon Yung Gee / David Schapiro / Amar J. Majmundar / Carolin E. Sadowski / Werner L. Pabst /
    Ankana Daga / Amelie T. van der Ven / Johanna M. Schmidt / Boon Chuan Low / Anjali Bansal Gupta / Brajendra K. Tripathi / Jenny Wong / Kirk Campbell / Kay Metcalfe / Denny Schanze / Tetsuya Niihori / Hiroshi Kaito / Kandai Nozu / Hiroyasu Tsukaguchi / Ryojiro Tanaka / Kiyoshi Hamahira / Yasuko Kobayashi / Takumi Takizawa / Ryo Funayama / Keiko Nakayama / Yoko Aoki / Naonori Kumagai / Kazumoto Iijima / Henry Fehrenbach / Jameela A. Kari / Sherif El Desoky / Sawsan Jalalah / Radovan Bogdanovic / Nataša Stajić / Hildegard Zappel / Assel Rakhmetova / Sharon-Rose Wassmer / Therese Jungraithmayr / Juergen Strehlau / Aravind Selvin Kumar / Arvind Bagga / Neveen A. Soliman / Shrikant M. Mane / Lewis Kaufman / Douglas R. Lowy / Mohamad A. Jairajpuri / Richard P. Lifton / York Pei / Martin Zenker / Shigeo Kure / Friedhelm Hildebrandt

    Nature Communications, Vol 9, Iss 1, Pp 1-

    2018  Volume 14

    Abstract: Nephrotic syndrome is the second most common chronic kidney disease but there are no targeted treatment strategies available. Here the authors identify mutations of six genes codifying for proteins involved in cytoskeleton remodelling and modulation of ... ...

    Abstract Nephrotic syndrome is the second most common chronic kidney disease but there are no targeted treatment strategies available. Here the authors identify mutations of six genes codifying for proteins involved in cytoskeleton remodelling and modulation of small GTPases in 17 families with nephrotic syndrome.
    Keywords Science ; Q
    Language English
    Publishing date 2018-05-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria

    Alexander Teumer / Yong Li / Sahar Ghasemi / Bram P. Prins / Matthias Wuttke / Tobias Hermle / Ayush Giri / Karsten B. Sieber / Chengxiang Qiu / Holger Kirsten / Adrienne Tin / Audrey Y. Chu / Nisha Bansal / Mary F. Feitosa / Lihua Wang / Jin-Fang Chai / Massimiliano Cocca / Christian Fuchsberger / Mathias Gorski /
    Anselm Hoppmann / Katrin Horn / Man Li / Jonathan Marten / Damia Noce / Teresa Nutile / Sanaz Sedaghat / Gardar Sveinbjornsson / Bamidele O. Tayo / Peter J. van der Most / Yizhe Xu / Zhi Yu / Lea Gerstner / Johan Ärnlöv / Stephan J. L. Bakker / Daniela Baptista / Mary L. Biggs / Eric Boerwinkle / Hermann Brenner / Ralph Burkhardt / Robert J. Carroll / Miao-Li Chee / Miao-Ling Chee / Mengmeng Chen / Ching-Yu Cheng / James P. Cook / Josef Coresh / Tanguy Corre / John Danesh / Martin H. de Borst / Alessandro De Grandi / Renée de Mutsert / Aiko P. J. de Vries / Frauke Degenhardt / Katalin Dittrich / Jasmin Divers / Kai-Uwe Eckardt / Georg Ehret / Karlhans Endlich / Janine F. Felix / Oscar H. Franco / Andre Franke / Barry I. Freedman / Sandra Freitag-Wolf / Ron T. Gansevoort / Vilmantas Giedraitis / Martin Gögele / Franziska Grundner-Culemann / Daniel F. Gudbjartsson / Vilmundur Gudnason / Pavel Hamet / Tamara B. Harris / Andrew A. Hicks / Hilma Holm / Valencia Hui Xian Foo / Shih-Jen Hwang / M. Arfan Ikram / Erik Ingelsson / Vincent W. V. Jaddoe / Johanna Jakobsdottir / Navya Shilpa Josyula / Bettina Jung / Mika Kähönen / Chiea-Chuen Khor / Wieland Kiess / Wolfgang Koenig / Antje Körner / Peter Kovacs / Holly Kramer / Bernhard K. Krämer / Florian Kronenberg / Leslie A. Lange / Carl D. Langefeld / Jeannette Jen-Mai Lee / Terho Lehtimäki / Wolfgang Lieb / Su-Chi Lim / Lars Lind / Cecilia M. Lindgren / Jianjun Liu / Markus Loeffler / Leo-Pekka Lyytikäinen / Anubha Mahajan / Joseph C. Maranville / Deborah Mascalzoni / Barbara McMullen / Christa Meisinger / Thomas Meitinger / Kozeta Miliku / Dennis O. Mook-Kanamori / Martina Müller-Nurasyid / Josyf C. Mychaleckyj / Matthias Nauck / Kjell Nikus / Boting Ning / Raymond Noordam / Jeffrey O’ Connell / Isleifur Olafsson / Nicholette D. Palmer / Annette Peters / Anna I. Podgornaia / Belen Ponte / Tanja Poulain / Peter P. Pramstaller / Ton J. Rabelink / Laura M. Raffield / Dermot F. Reilly / Rainer Rettig / Myriam Rheinberger / Kenneth M. Rice / Fernando Rivadeneira / Heiko Runz / Kathleen A. Ryan / Charumathi Sabanayagam / Kai-Uwe Saum / Ben Schöttker / Christian M. Shaffer / Yuan Shi / Albert V. Smith / Konstantin Strauch / Michael Stumvoll / Benjamin B. Sun / Silke Szymczak / E-Shyong Tai / Nicholas Y. Q. Tan / Kent D. Taylor / Andrej Teren / Yih-Chung Tham / Joachim Thiery / Chris H. L. Thio / Hauke Thomsen / Unnur Thorsteinsdottir / Anke Tönjes / Johanne Tremblay / André G. Uitterlinden / Pim van der Harst / Niek Verweij / Suzanne Vogelezang / Uwe Völker / Melanie Waldenberger / Chaolong Wang / Otis D. Wilson / Charlene Wong / Tien-Yin Wong / Qiong Yang / Masayuki Yasuda / Shreeram Akilesh / Murielle Bochud / Carsten A. Böger / Olivier Devuyst / Todd L. Edwards / Kevin Ho / Andrew P. Morris / Afshin Parsa / Sarah A. Pendergrass / Bruce M. Psaty / Jerome I. Rotter / Kari Stefansson / James G. Wilson / Katalin Susztak / Harold Snieder / Iris M. Heid / Markus Scholz / Adam S. Butterworth / Adriana M. Hung / Cristian Pattaro / Anna Köttgen

    Nature Communications, Vol 10, Iss 1, Pp 1-

    2019  Volume 19

    Abstract: Urinary albumin-to-creatinine ratio (UCAR) is associated with various clinical outcomes such as kidney disease and cardiovascular disease. Here, the authors report genome-wide meta-analysis in over 500,000 individuals and find 68 UACR loci, followed by ... ...

    Abstract Urinary albumin-to-creatinine ratio (UCAR) is associated with various clinical outcomes such as kidney disease and cardiovascular disease. Here, the authors report genome-wide meta-analysis in over 500,000 individuals and find 68 UACR loci, followed by statistical fine-mapping, gene prioritization and experimental validation in flies.
    Keywords Science ; Q
    Language English
    Publishing date 2019-09-01T00:00:00Z
    Publisher Nature Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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