Fibronectin is up‐regulated in podocytes by mechanical stress

  • Felix Kliewe
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Sören Kaling
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Henriette Lötzsch
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Nadine Artelt
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Maximilian Schindler
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Henrik Rogge
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Sindy Schröder
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Christian Scharf
    Department of Ear, Nose, and Throat Diseases University Medicine Greifswald Greifswald Germany
  • Kerstin Amann
    Department of Nephropathology University Medicine Erlangen Erlangen Germany
  • Christoph Daniel
    Department of Nephropathology University Medicine Erlangen Erlangen Germany
  • Maja T. Lindenmeyer
    III Department of Medicine University Medical Center Hamburg‐Eppendorf Hamburg Germany
  • Clemens D. Cohen
    Nephrological Center, Medical Clinic and Policlinic IV University of Munich Munich Germany
  • Karlhans Endlich
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany
  • Nicole Endlich
    Department of Anatomy and Cell Biology University Medicine Greifswald Greifswald Germany

抄録

<jats:p>Hypertension is one of the central causes of kidney damage. In the past it was shown that glomerular hypertension leads to morphologic changes of podocytes and effacement and is responsible for detachment of these postmitotic cells. Because we have shown that podocytes are mechanosensitive and respond to mechanical stress by reorganization of the actin cytoskeleton <jats:italic>in vitro</jats:italic>, we look for mechanotransducers in podocytes. In this study, we demonstrate that the extracellular matrix protein fibronectin (Fn1) might be a potential candidate. The present study shows that Fn1 is essential for the attachment of podocytes during mechanical stress. By real‐time quantitative PCR as well as by liquid chromatography‐mass spectrometry, we found a significant up‐regulation of Fn1 caused by mechanical stretch (3 d, 0.5 Hz, and 5% extension). To study the role of Fn1 in cultured podocytes under mechanical stress, Fn1 was knocked down (Fn1 KD) by a specific small interfering RNA. Additionally, we established a Fn1 knockout (KO) podocyte cell line (Fn1 KO) by clustered regularly interspaced short palindromic repeats (CRISPR)/ CRISPR‐associated protein 9 (Cas9). During mechanical stress, a significant loss of podocytes (>80%) was observed in Fn1 KD as well as Fn1 KO podocytes compared with control cells. Furthermore, Fn1 KO podocytes showed a significant down‐regulation of the focal adhesion proteins talin, vinculin, and paxillin and a reduced cell spreading, indicating an important role of Fn1 in adhesion. Analyses of kidney sections from patients with diabetic nephropathy have shown a significant up‐regulation of FN1 in contrast to control biopsies. In summary, we show that Fn1 plays an important role in the adaptation of podocytes to mechanical stress.—Kliewe, F., Kaling, S., Lötzsch, H., Artelt, N., Schindler, M., Rogge, H., Schröder, S., Scharf, C., Amann, K., Daniel, C., Lindenmeyer, M. T., Cohen, C. D., Endlich, K., Endlich, N. Fibronectin is up‐regulated in podocytes by mechanical stress. FASEB J. 33, 14450‐14460 (2019). <jats:ext-link xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="http://www.fasebj.org">www.fasebj.org</jats:ext-link></jats:p>

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