Butyrate upregulates stromelysin-1 production by intestinal mesenchymal cells
Butyrate upregulates stromelysin-1 production by intestinal mesenchymal cells
Nutritional factors and resident bacteria participate in the pathogenesis of intestinal inflammation. However, the ways in which bacteria and complex diets might modulate matrix metalloproteinase (MMP) production are unknown. We hypothesized that butyrate might enhance production of MMPs, thus amplifying their response to signals in inflammatory conditions. Human mesenchymal cells were incubated with butyrate and then stimulated with cytokines. MMPs and inhibitors were studied by Western blotting and quantitative RT-PCR. Acetylation of histones was examined in Triton X acetic acid-urea gels by PAGE. We showed that butyrate selectively enhanced the protein production and mRNA expression of stromelysin-1 in tumor necrosis factor-alpha- or interleukin-1beta-stimulated mesenchymal cells. Butyrate alone did not induce any change in MMP production or mRNA expression. It increased the acetylation of histones in mesenchymal cells. Furthermore, acetylation of histones (induced by trichostatin A) reproduced the effects of butyrate. Although butyrate is a major source of nutrient for the colonic epithelial cells, it modulates intestinal inflammation through the secretion of stromelysin-1 in stimulated stromal cells via the inhibition of histone deacetylase.
G918-G924
Pender, Sylvia L.F.
62528b03-ec42-41bb-80fe-48454c2c5242
Quinn, Jessica J.
15522eaa-9990-4365-b8c0-fac3fa2776a9
Sanderson, Ian R.
7dd888f3-87ad-4a33-aef2-4b2e453046ad
MacDonald, Thomas T.
a6bde8a9-acc4-4128-851f-dd5dbfe28816
November 2000
Pender, Sylvia L.F.
62528b03-ec42-41bb-80fe-48454c2c5242
Quinn, Jessica J.
15522eaa-9990-4365-b8c0-fac3fa2776a9
Sanderson, Ian R.
7dd888f3-87ad-4a33-aef2-4b2e453046ad
MacDonald, Thomas T.
a6bde8a9-acc4-4128-851f-dd5dbfe28816
Pender, Sylvia L.F., Quinn, Jessica J., Sanderson, Ian R. and MacDonald, Thomas T.
(2000)
Butyrate upregulates stromelysin-1 production by intestinal mesenchymal cells.
American Journal of Physiology: Gastrointestinal and Liver Physiology, 279 (5), .
Abstract
Nutritional factors and resident bacteria participate in the pathogenesis of intestinal inflammation. However, the ways in which bacteria and complex diets might modulate matrix metalloproteinase (MMP) production are unknown. We hypothesized that butyrate might enhance production of MMPs, thus amplifying their response to signals in inflammatory conditions. Human mesenchymal cells were incubated with butyrate and then stimulated with cytokines. MMPs and inhibitors were studied by Western blotting and quantitative RT-PCR. Acetylation of histones was examined in Triton X acetic acid-urea gels by PAGE. We showed that butyrate selectively enhanced the protein production and mRNA expression of stromelysin-1 in tumor necrosis factor-alpha- or interleukin-1beta-stimulated mesenchymal cells. Butyrate alone did not induce any change in MMP production or mRNA expression. It increased the acetylation of histones in mesenchymal cells. Furthermore, acetylation of histones (induced by trichostatin A) reproduced the effects of butyrate. Although butyrate is a major source of nutrient for the colonic epithelial cells, it modulates intestinal inflammation through the secretion of stromelysin-1 in stimulated stromal cells via the inhibition of histone deacetylase.
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Published date: November 2000
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Local EPrints ID: 73598
URI: http://eprints.soton.ac.uk/id/eprint/73598
ISSN: 0193-1857
PURE UUID: 79aea6c1-f4e0-4ac6-8919-bd0ee047944e
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Date deposited: 10 Mar 2010
Last modified: 09 Jan 2022 03:05
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Author:
Jessica J. Quinn
Author:
Ian R. Sanderson
Author:
Thomas T. MacDonald
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