Literature DB >> 29777019

Cellular Origin and Functional Relevance of Collagen I Production in the Kidney.

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.
Copyright © 2018 by the American Society of Nephrology.

Entities:  

Keywords:  chronic kidney disease; chronic renal failure; fibrosis; immunology; interstitial fibrosis

Mesh:

Substances:

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


  49 in total

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4.  Morphometric and visual evaluation of fibrosis in renal biopsies.

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7.  Fibrocytes develop outside the kidney but contribute to renal fibrosis in a mouse model.

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5.  Fibrosis and Immune Cell Infiltration Are Separate Events Regulated by Cell-Specific Receptor Notch3 Expression.

Authors:  Sabine Brandt; Tobias M Ballhause; Anja Bernhardt; Annika Becker; Delia Salaru; Hien Minh Le-Deffge; Alexander Fehr; Yan Fu; Lars Philipsen; Sonja Djudjaj; Andreas J Müller; Rafael Kramann; Mahmoud Ibrahim; Robert Geffers; Chris Siebel; Berend Isermann; Florian H Heidel; Jonathan A Lindquist; Peter R Mertens
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6.  TGF-β promotes fibrosis after severe acute kidney injury by enhancing renal macrophage infiltration.

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Review 7.  Application of Histone Deacetylase Inhibitors in Renal Interstitial Fibrosis.

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10.  Neural transcription factor Pou4f1 promotes renal fibrosis via macrophage-myofibroblast transition.

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