Mitochondrial alterations induced by aspirin in rat hepatocytes expressing mitochondrially targeted green fluorescent protein (mtGFP)

Mitochondria in primary living hepatocytes were visualized in cells transfected with a chimeric plasmid encoding for the green fluorescent protein (GFP) of Aequorea victoria engineered to be specifically targeted to mitochondria, as described recently (Rizzuto et al. (1995) Curr. Biol. 5, 635–642)....

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Veröffentlicht in:FEBS letters 1996-03, Vol.382 (3), p.256-260
Hauptverfasser: Venerando, R., Miotto, G., Pizzo, P., Rizzuto, R., Siliprandi, N.
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container_end_page 260
container_issue 3
container_start_page 256
container_title FEBS letters
container_volume 382
creator Venerando, R.
Miotto, G.
Pizzo, P.
Rizzuto, R.
Siliprandi, N.
description Mitochondria in primary living hepatocytes were visualized in cells transfected with a chimeric plasmid encoding for the green fluorescent protein (GFP) of Aequorea victoria engineered to be specifically targeted to mitochondria, as described recently (Rizzuto et al. (1995) Curr. Biol. 5, 635–642). The identification of the fluorescent organelles as authentic mitochondria was confirmed by double labeling with rhodamine 123. Acetylsalicylate treatment of hepatocytes induced in mitochondria typical morphological alterations closely analogous to the swelling promoted by acetylsalicylate in isolated mitochondria. Cyclosporin A, which in isolated mitochondria prevents the changes induced by acetylsalicylate, had no protective action but induced per se specific alterations in the morphology of mitochondria. Moreover, exposure of hepatocytes to cyclosporin A followed by acetylsalicylate caused the same mitochondrial changes induced by each of the two compounds separately. The structural alterations caused by acetylsalicylate were constantly associated with a decrease in mitochondrial urea synthesis and cell viability.
doi_str_mv 10.1016/0014-5793(96)00182-2
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(1995) Curr. Biol. 5, 635–642). The identification of the fluorescent organelles as authentic mitochondria was confirmed by double labeling with rhodamine 123. Acetylsalicylate treatment of hepatocytes induced in mitochondria typical morphological alterations closely analogous to the swelling promoted by acetylsalicylate in isolated mitochondria. Cyclosporin A, which in isolated mitochondria prevents the changes induced by acetylsalicylate, had no protective action but induced per se specific alterations in the morphology of mitochondria. Moreover, exposure of hepatocytes to cyclosporin A followed by acetylsalicylate caused the same mitochondrial changes induced by each of the two compounds separately. The structural alterations caused by acetylsalicylate were constantly associated with a decrease in mitochondrial urea synthesis and cell viability.</description><subject>Acetylsalicylate</subject><subject>Animals</subject><subject>ASA</subject><subject>Aspirin - pharmacology</subject><subject>Cell Survival</subject><subject>Cells, Cultured</subject><subject>CsA</subject><subject>cyclosporin</subject><subject>Cyclosporin A</subject><subject>Cyclosporine - pharmacology</subject><subject>Fluorescent Dyes</subject><subject>GFP</subject><subject>Green Fluorescent Proteins</subject><subject>Hepatocyte</subject><subject>Luminescent Proteins - biosynthesis</subject><subject>Luminescent Proteins - genetics</subject><subject>Male</subject><subject>membrane permeability transition</subject><subject>Mitochondria, Liver - drug effects</subject><subject>Mitochondria, Liver - metabolism</subject><subject>mitochondrially targeted green fluorescent protein</subject><subject>MPT</subject><subject>mtGFP</subject><subject>Rat liver mitochondria</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Rhodamine 123</subject><subject>Rhodamines</subject><subject>Transfection</subject><subject>Urea - metabolism</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc9u1DAQxi0EKtvCG4DkE2oPAf_bOLkglarbIhXBAc6W44y3rhIntZ3SPEDfu053VfWEOFkz3ze_GX1G6AMlnymh5RdCqCjWsubHdXmSi4oV7BVa0Urygouyeo1Wz5a36DDGG7K4aH2ADqqSrOuKrNDDD5cGcz34NjjdYd0lCDq5wUfsfDsZaHEzYx1HF5zPLZxVfA2jzlNzgojhfgwQo_Nb3L9EdTNOOmwhZcI2AHhsu2nIVgM-4TEMCTLtuE8Xm18n79Abq7sI7_fvEfqzOf99dllc_bz4fnZ6VRjBCCu4sYQJKBuorGlqtm4bSaS1IExJhIHGSG0F1bzhRhjRSl5Koq0mTdVqwoEfoU87bt5_O0FMqnf5oK7THoYpKinrnAwV2Sh2RhOGGANYNQbX6zArStSSvlqiVUu0qn4qKqZYHvu4509ND-3z0D7urG92-l_XwfxfTLU5_8YWYenX5VN3WfR1B4Kc1p2DoKJx4PN3uQAmqXZw_770EQltq4M</recordid><startdate>19960318</startdate><enddate>19960318</enddate><creator>Venerando, R.</creator><creator>Miotto, G.</creator><creator>Pizzo, P.</creator><creator>Rizzuto, R.</creator><creator>Siliprandi, N.</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19960318</creationdate><title>Mitochondrial alterations induced by aspirin in rat hepatocytes expressing mitochondrially targeted green fluorescent protein (mtGFP)</title><author>Venerando, R. ; Miotto, G. ; Pizzo, P. ; Rizzuto, R. ; Siliprandi, N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4202-3cf024e6be8fcb925db707ffe4c604cebc7af41a3b3c4c4d73670afa0b8da03e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Acetylsalicylate</topic><topic>Animals</topic><topic>ASA</topic><topic>Aspirin - pharmacology</topic><topic>Cell Survival</topic><topic>Cells, Cultured</topic><topic>CsA</topic><topic>cyclosporin</topic><topic>Cyclosporin A</topic><topic>Cyclosporine - pharmacology</topic><topic>Fluorescent Dyes</topic><topic>GFP</topic><topic>Green Fluorescent Proteins</topic><topic>Hepatocyte</topic><topic>Luminescent Proteins - biosynthesis</topic><topic>Luminescent Proteins - genetics</topic><topic>Male</topic><topic>membrane permeability transition</topic><topic>Mitochondria, Liver - drug effects</topic><topic>Mitochondria, Liver - metabolism</topic><topic>mitochondrially targeted green fluorescent protein</topic><topic>MPT</topic><topic>mtGFP</topic><topic>Rat liver mitochondria</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Rhodamine 123</topic><topic>Rhodamines</topic><topic>Transfection</topic><topic>Urea - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Venerando, R.</creatorcontrib><creatorcontrib>Miotto, G.</creatorcontrib><creatorcontrib>Pizzo, P.</creatorcontrib><creatorcontrib>Rizzuto, R.</creatorcontrib><creatorcontrib>Siliprandi, N.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Venerando, R.</au><au>Miotto, G.</au><au>Pizzo, P.</au><au>Rizzuto, R.</au><au>Siliprandi, N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mitochondrial alterations induced by aspirin in rat hepatocytes expressing mitochondrially targeted green fluorescent protein (mtGFP)</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>1996-03-18</date><risdate>1996</risdate><volume>382</volume><issue>3</issue><spage>256</spage><epage>260</epage><pages>256-260</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>Mitochondria in primary living hepatocytes were visualized in cells transfected with a chimeric plasmid encoding for the green fluorescent protein (GFP) of Aequorea victoria engineered to be specifically targeted to mitochondria, as described recently (Rizzuto et al. (1995) Curr. Biol. 5, 635–642). The identification of the fluorescent organelles as authentic mitochondria was confirmed by double labeling with rhodamine 123. Acetylsalicylate treatment of hepatocytes induced in mitochondria typical morphological alterations closely analogous to the swelling promoted by acetylsalicylate in isolated mitochondria. Cyclosporin A, which in isolated mitochondria prevents the changes induced by acetylsalicylate, had no protective action but induced per se specific alterations in the morphology of mitochondria. Moreover, exposure of hepatocytes to cyclosporin A followed by acetylsalicylate caused the same mitochondrial changes induced by each of the two compounds separately. 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source Wiley Online Library - AutoHoldings Journals; MEDLINE; Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection
subjects Acetylsalicylate
Animals
ASA
Aspirin - pharmacology
Cell Survival
Cells, Cultured
CsA
cyclosporin
Cyclosporin A
Cyclosporine - pharmacology
Fluorescent Dyes
GFP
Green Fluorescent Proteins
Hepatocyte
Luminescent Proteins - biosynthesis
Luminescent Proteins - genetics
Male
membrane permeability transition
Mitochondria, Liver - drug effects
Mitochondria, Liver - metabolism
mitochondrially targeted green fluorescent protein
MPT
mtGFP
Rat liver mitochondria
Rats
Rats, Wistar
Rhodamine 123
Rhodamines
Transfection
Urea - metabolism
title Mitochondrial alterations induced by aspirin in rat hepatocytes expressing mitochondrially targeted green fluorescent protein (mtGFP)
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