Inhibition of tyrosine kinase receptor signaling attenuates fibrogenesis in an ex vivo model of human renal fibrosisBigaeva, E., Stribos, E. G. D., Mutsaers, H. A. M., Piersma, B., Leliveld, A. M., de Jong, I. J., Bank, R. A., Seelen, M. A., van Goor, H., Wollin, L., Olinga, P. & Boersema, M., Jan-2020, In : American journal of physiology-Renal physiology. 318, 1, p. F117-F134 18 p.
Research output: Contribution to journal › Article › Academic › peer-review
- Pharmaceutical Technology and Biopharmacy
- Center for Medical Imaging (CMI)
- Guided Treatment in Optimal Selected Cancer Patients (GUTS)
- Groningen Kidney Center (GKC)
- Restoring Organ Function by Means of Regenerative Medicine (REGENERATE)
- Groningen Institute for Organ Transplantation (GIOT)
- Biopharmaceuticals, Discovery, Design and Delivery (BDDD)
- Pharmacokinetics, Toxicology and Targeting
Poor translation from animal studies to human clinical trials is one of the main hurdles in the development of new drugs. Here, we used precision-cut kidney slices (PCKS) as a translational model to study renal fibrosis and to investigate whether inhibition of tyrosine kinase receptors, with the selective inhibitor nintedanib, can halt fibrosis in murine and human PCKS. We used renal tissue of murine and human origins to obtain PCKS. Control slices and slices treated with nintedanib were studied to assess viability, activation of tyrosine kinase receptors, cell proliferation, collagen type I accumulation, and gene and protein regulation. During culture, PCKS spontaneously develop a fibrotic response that resembles in vivo fibrogenesis. Nintedanib blocked culture-induced phosphorylation of platelet-derived growth factor receptor and vascular endothelial growth factor receptor. Furthermore, nintedanib inhibited cell proliferation and reduced collagen type I accumulation and expression of fibrosis-related genes in healthy murine and human PCKS. Modulation of extracellular matrix homeostasis was achieved already at 0.1 mu M, whereas high concentrations (1 and 5 mu M) elicited possible nonselective effects. In PCKS from human diseased renal tissue, nintedanib showed limited capacity to reverse established fibrosis. In conclusion, nintedanib attenuated the onset of fibrosis in both murine and human PCKS by inhibiting the phosphorylation of tyrosine kinase receptors: however, the reversal of established fibrosis was not achieved.
|Number of pages||18|
|Journal||American journal of physiology-Renal physiology|
|Early online date||18-Nov-2019|
|Publication status||Published - Jan-2020|
- nintedanib, precision-cut kidney slices, renal fibrosis, tyrosine kinase receptor, CUT KIDNEY SLICES, GROWTH-FACTOR, ANGIOKINASE INHIBITOR, LIVER SLICES, CELL CANCER, EARLY-ONSET, BIBF 1120, NINTEDANIB, EXPRESSION, ANGIOGENESIS