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Open AccessJournal ArticleDOI

Mast cells: the forgotten cells of renal fibrosis

Ian Roberts, +1 more
- 01 Nov 2000 - 
- Vol. 53, Iss: 11, pp 858-862
TLDR
An increased number ofmast cells is a consistent feature of renal fibrosis, whatever the underlying pathology, and the number of mast cells correlates with the extent of interstitial fibrosis; this suggests that mast cells might play a pathogenetic role in the fibrotic process.
Abstract
Background/Aims—Mast cells, when activated, secrete a large number of fibrogenic factors and have been implicated in the development of fibrotic conditions of the liver, lung, and skin. There is evidence that renal fibrosis is closely linked with a chronic inflammatory cell infiltrate within the interstitium, but a potential role for mast cells in this process has yet to be defined. Therefore, the numbers of mast cells in normal and fibrotic kidneys with various pathologies were investigated. Methods—Mast cells were quantified in renal transplants showing acute and chronic rejection and cyclosporin toxicity, kidneys removed for chronic pyelonephritis, and renal biopsies from patients with IgA nephropathy,membranous nephropathy, and diabetic nephropathy. Mast cells were stained using two methods: acid toluidine blue detected less than 30% of the mast cells revealed by immunohistochemistry for mast cell tryptase. Results—Mast cells were scarce or absent in normal kidney (median, 1.6 mast cells/mm 2 ) but numerous throughout the cortex and medulla in all specimens that showed fibrosis. They were almost entirely confined to the renal interstitium. Mast cells were present in large numbers in biopsies from patients with membranous nephropathy (median, 21.7 mast cells/ mm 2 ) and diabetic nephropathy (median, 29.2 mast cells/mm 2

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Citations
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References
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Journal ArticleDOI

Decrease of mast cells in w/wv mice and their increase by bone marrow transplantation.

TL;DR: The results show that the W/Wv mouse is a useful tool for the investigations concerning the physiologic roles and the origin of mast cells.
Journal ArticleDOI

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TL;DR: Binding was not detected on 3T3 fibroblasts carrying the steel (Sl) mutation, confirming the biological significance of the binding activity and demonstrating that mutations at the Sl locus affect the expression or structure of the kit ligand.
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Human mast cells stimulate vascular tube formation. Tryptase is a novel, potent angiogenic factor.

TL;DR: The results suggest that mast cells act at sites of new vessel formation by secreting tryptase, which then functions as a potent and previously unrecognized angiogenic factor.
Journal ArticleDOI

Human mast cell chymase and leukocyte elastase release latent transforming growth factor-beta 1 from the extracellular matrix of cultured human epithelial and endothelial cells.

TL;DR: The release of TGF-β from the matrix by leukocyte and mast cell enzymes may contribute to the accumulation of connective tissue in inflammation.
Journal ArticleDOI

Tubular epithelial-myofibroblast transdifferentiation in progressive tubulointerstitial fibrosis in 5/6 nephrectomized rats

TL;DR: P phenotypic and morphological evidence is provided to support the hypothesis that TEC are pro-fibrogenitor cells capable of tubular epithelial-myofibroblast transdifferentiation in progressive renal fibrosis.
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