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Cellular Origin and Functional Relevance of Collagen I Production in the Kidney.
Buchtler, Simone; Grill, Alexandra; Hofmarksrichter, Stefanie; Stöckert, Petra; Schiechl-Brachner, Gabriela; Rodriguez Gomez, Manuel; Neumayer, Sophia; Schmidbauer, Kathrin; Talke, Yvonne; Klinkhammer, Barbara M; Boor, Peter; Medvinsky, Alexander; Renner, Kerstin; Castrop, Hayo; Mack, Matthias.
Afiliação
  • Buchtler S; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Grill A; Institute of Physiology, University of Regensburg, Regensburg, Germany.
  • Hofmarksrichter S; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Stöckert P; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Schiechl-Brachner G; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Rodriguez Gomez M; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Neumayer S; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Schmidbauer K; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Talke Y; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
  • Klinkhammer BM; Department of Pathology and.
  • Boor P; Department of Nephrology, RWTH Aachen University, Aachen, Germany; and.
  • Medvinsky A; Department of Pathology and.
  • Renner K; Department of Nephrology, RWTH Aachen University, Aachen, Germany; and.
  • Castrop H; Institute for Stem Cell Research, Medical Research Council Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom.
  • Mack M; Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.
J Am Soc Nephrol ; 29(7): 1859-1873, 2018 07.
Article em En | MEDLINE | ID: mdl-29777019
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colágeno Tipo I / Insuficiência Renal Crônica / Injúria Renal Aguda / Rim Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Colágeno Tipo I / Insuficiência Renal Crônica / Injúria Renal Aguda / Rim Idioma: En Ano de publicação: 2018 Tipo de documento: Article