| Literature DB >> 29777019 |
Simone Buchtler1, Alexandra Grill2, Stefanie Hofmarksrichter1, Petra Stöckert1, Gabriela Schiechl-Brachner1, Manuel Rodriguez Gomez1, Sophia Neumayer1, Kathrin Schmidbauer1, Yvonne Talke1, Barbara M Klinkhammer3,4, Peter Boor3,4, Alexander Medvinsky5, Kerstin Renner1, Hayo Castrop2, Matthias Mack6.
Abstract
Background Interstitial fibrosis is associated with chronic renal failure. In addition to fibroblasts, bone marrow-derived cells and tubular epithelial cells have the capacity to produce collagen. However, the amount of collagen produced by each of these cell types and the relevance of fibrosis to renal function are unclear.Methods We generated conditional cell type-specific collagen I knockout mice and used (reversible) unilateral ureteral obstruction and adenine-induced nephropathy to study renal fibrosis and function.Results In these mouse models, hematopoietic, bone marrow-derived cells contributed to 38%-50% of the overall deposition of collagen I in the kidney. The influence of fibrosis on renal function was dependent on the type of damage. In unilateral ureteral obstruction, collagen production by resident fibroblasts was essential to preserve renal function, whereas in the chronic model of adenine-induced nephropathy, collagen production was detrimental to renal function.Conclusions Our data show that hematopoietic cells are a major source of collagen and that antifibrotic therapies need to be carefully considered depending on the type of disease and the underlying cause of fibrosis.Entities:
Keywords: chronic kidney disease; chronic renal failure; fibrosis; immunology; interstitial fibrosis
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Year: 2018 PMID: 29777019 PMCID: PMC6050926 DOI: 10.1681/ASN.2018020138
Source DB: PubMed Journal: J Am Soc Nephrol ISSN: 1046-6673 Impact factor: 10.121