• Nicole Endlich
  • Tim Lange
  • Jana Kuhn
  • Paul Klemm
  • Ahmed M Kotb
  • Florian Siegerist
  • Frances Kindt
  • Maja T Lindenmeyer
  • Clemens D Cohen
  • Andreas W Kuss
  • Neetika Nath
  • Rainer Rettig
  • Uwe Lendeckel
  • Uwe Zimmermann
  • Kerstin Amann
  • Sylvia Stracke
  • Karlhans Endlich


Podocyte loss and changes to the complex morphology are major causes of chronic kidney disease (CKD). As the incidence is continuously increasing over the last decades without sufficient treatment, it is important to find predicting biomarkers. Therefore, we measured urinary mRNA levels of podocyte genes NPHS1, NPHS2, PODXL and BDNF, KIM-1, CTSL by qRT-PCR of 120 CKD patients. We showed a strong correlation between BDNF and the kidney injury marker KIM-1, which were also correlated with NPHS1, suggesting podocytes as a contributing source. In human biopsies, BDNF was localized in the cell body and major processes of podocytes. In glomeruli of diabetic nephropathy patients, we found a strong BDNF signal in the remaining podocytes. An inhibition of the BDNF receptor TrkB resulted in enhanced podocyte dedifferentiation. The knockdown of the orthologue resulted in pericardial oedema formation and lowered viability of zebrafish larvae. We found an enlarged Bowman's space, dilated glomerular capillaries, podocyte loss and an impaired glomerular filtration. We demonstrated that BDNF is essential for glomerular development, morphology and function and the expression of BDNF and KIM-1 is highly correlated in urine cells of CKD patients. Therefore, BDNF mRNA in urine cells could serve as a potential CKD biomarker.

Bibliografische Daten

StatusVeröffentlicht - 11.2018
Extern publiziertJa
PubMed 30133147