TNF- alpha downregulates the leukotriene C sub(4) synthase gene in mononuclear phagocytes
We studied the effect of tumor necrosis factor (TNF)- alpha exposure on cysteinyl leukotriene (LT) synthesis by cells of monocyte/macrophage lineage. TNF- alpha conditioning of monocytic THP-1 cells and primary human monocytes resulted in a decreased capacity for LTC sub(4) release. TNF- alpha expos...
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Veröffentlicht in: | American journal of physiology. Lung cellular and molecular physiology 2007-01, Vol.292 (1), p.L215-L222 |
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description | We studied the effect of tumor necrosis factor (TNF)- alpha exposure on cysteinyl leukotriene (LT) synthesis by cells of monocyte/macrophage lineage. TNF- alpha conditioning of monocytic THP-1 cells and primary human monocytes resulted in a decreased capacity for LTC sub(4) release. TNF- alpha exposure (for 16-24 h) decreased LTC sub(4) synthase mRNA in THP-1 cells, primary mouse bone marrow-derived macrophages, and eosinophilic AML14.3D10 cells. TNF- alpha downregulated LTC sub(4) synthase mRNA in THP-1 cells in a dose- and time-dependent manner, with downregulation observed as early as 4 h. The effect of TNF- alpha on LTC sub(4) synthase mRNA expression was mediated via the MEK/ERK pathway, but not via cyclooxygenase or nitric oxide synthase pathways. Conditioning of actinomycin D-treated cells with TNF- alpha did not accelerate degradation of LTC sub(4) synthase mRNA. TNF- alpha produced sustained activation of p50 and p65, which were previously reported by our group to decrease LTC sub(4) synthase promoter activity. In transiently transfected THP-1 cells, TNF- alpha decreased promoter activity via an element located within the first 620 bp of the promoter. We conclude that TNF- alpha exposure downregulates the synthetic capacity for cysteinyl LT release and LTC sub(4) synthase gene expression in monocytes/macrophages via a transcriptional mechanism. |
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TNF- alpha conditioning of monocytic THP-1 cells and primary human monocytes resulted in a decreased capacity for LTC sub(4) release. TNF- alpha exposure (for 16-24 h) decreased LTC sub(4) synthase mRNA in THP-1 cells, primary mouse bone marrow-derived macrophages, and eosinophilic AML14.3D10 cells. TNF- alpha downregulated LTC sub(4) synthase mRNA in THP-1 cells in a dose- and time-dependent manner, with downregulation observed as early as 4 h. The effect of TNF- alpha on LTC sub(4) synthase mRNA expression was mediated via the MEK/ERK pathway, but not via cyclooxygenase or nitric oxide synthase pathways. Conditioning of actinomycin D-treated cells with TNF- alpha did not accelerate degradation of LTC sub(4) synthase mRNA. TNF- alpha produced sustained activation of p50 and p65, which were previously reported by our group to decrease LTC sub(4) synthase promoter activity. In transiently transfected THP-1 cells, TNF- alpha decreased promoter activity via an element located within the first 620 bp of the promoter. We conclude that TNF- alpha exposure downregulates the synthetic capacity for cysteinyl LT release and LTC sub(4) synthase gene expression in monocytes/macrophages via a transcriptional mechanism.</description><identifier>ISSN: 1040-0605</identifier><language>eng</language><ispartof>American journal of physiology. 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TNF- alpha conditioning of monocytic THP-1 cells and primary human monocytes resulted in a decreased capacity for LTC sub(4) release. TNF- alpha exposure (for 16-24 h) decreased LTC sub(4) synthase mRNA in THP-1 cells, primary mouse bone marrow-derived macrophages, and eosinophilic AML14.3D10 cells. TNF- alpha downregulated LTC sub(4) synthase mRNA in THP-1 cells in a dose- and time-dependent manner, with downregulation observed as early as 4 h. The effect of TNF- alpha on LTC sub(4) synthase mRNA expression was mediated via the MEK/ERK pathway, but not via cyclooxygenase or nitric oxide synthase pathways. Conditioning of actinomycin D-treated cells with TNF- alpha did not accelerate degradation of LTC sub(4) synthase mRNA. TNF- alpha produced sustained activation of p50 and p65, which were previously reported by our group to decrease LTC sub(4) synthase promoter activity. In transiently transfected THP-1 cells, TNF- alpha decreased promoter activity via an element located within the first 620 bp of the promoter. We conclude that TNF- alpha exposure downregulates the synthetic capacity for cysteinyl LT release and LTC sub(4) synthase gene expression in monocytes/macrophages via a transcriptional mechanism.</description><issn>1040-0605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqNjMsKgkAUQGdRkD3-4a6iFsIVH-Raklat3LSSyW5qjTPmnSH8-wz6gFYHDoczE16AEfqYYLwQS-YHIsaIiScuxTn3Qaq-kXAzbz1Q7ZS0xGAbAkXuaezQkibIgN11F-2BR20byQT1V7caOqONdpUiOcD0qU01ToO1mN-lYtr8uBLb_FhkJ78fzMsR27JruSKlpCbjuAzSQ5SGQRz-HX4AyWhEiw</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Serio, Kenneth J</creator><creator>Luo, Colin</creator><creator>Luo, Linda</creator><creator>Mao, Jenny T</creator><scope>7T5</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>20070101</creationdate><title>TNF- alpha downregulates the leukotriene C sub(4) synthase gene in mononuclear phagocytes</title><author>Serio, Kenneth J ; Luo, Colin ; Luo, Linda ; Mao, Jenny T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_198493153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Serio, Kenneth J</creatorcontrib><creatorcontrib>Luo, Colin</creatorcontrib><creatorcontrib>Luo, Linda</creatorcontrib><creatorcontrib>Mao, Jenny T</creatorcontrib><collection>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Serio, Kenneth J</au><au>Luo, Colin</au><au>Luo, Linda</au><au>Mao, Jenny T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>TNF- alpha downregulates the leukotriene C sub(4) synthase gene in mononuclear phagocytes</atitle><jtitle>American journal of physiology. Lung cellular and molecular physiology</jtitle><date>2007-01-01</date><risdate>2007</risdate><volume>292</volume><issue>1</issue><spage>L215</spage><epage>L222</epage><pages>L215-L222</pages><issn>1040-0605</issn><abstract>We studied the effect of tumor necrosis factor (TNF)- alpha exposure on cysteinyl leukotriene (LT) synthesis by cells of monocyte/macrophage lineage. TNF- alpha conditioning of monocytic THP-1 cells and primary human monocytes resulted in a decreased capacity for LTC sub(4) release. TNF- alpha exposure (for 16-24 h) decreased LTC sub(4) synthase mRNA in THP-1 cells, primary mouse bone marrow-derived macrophages, and eosinophilic AML14.3D10 cells. TNF- alpha downregulated LTC sub(4) synthase mRNA in THP-1 cells in a dose- and time-dependent manner, with downregulation observed as early as 4 h. The effect of TNF- alpha on LTC sub(4) synthase mRNA expression was mediated via the MEK/ERK pathway, but not via cyclooxygenase or nitric oxide synthase pathways. Conditioning of actinomycin D-treated cells with TNF- alpha did not accelerate degradation of LTC sub(4) synthase mRNA. TNF- alpha produced sustained activation of p50 and p65, which were previously reported by our group to decrease LTC sub(4) synthase promoter activity. In transiently transfected THP-1 cells, TNF- alpha decreased promoter activity via an element located within the first 620 bp of the promoter. We conclude that TNF- alpha exposure downregulates the synthetic capacity for cysteinyl LT release and LTC sub(4) synthase gene expression in monocytes/macrophages via a transcriptional mechanism.</abstract></addata></record> |
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title | TNF- alpha downregulates the leukotriene C sub(4) synthase gene in mononuclear phagocytes |
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