Metallothionein and hsp70 expression in HepG2 cells after prolonged cadmium exposure
Cadmium is a widely distributed industrial and environmental pollutant. Principle target organs are soft tissues such as the liver, where cadmium accumulates with a biological half-life of approximately 20–30 years causing a variety of toxic responses. In HepG2, CdCl 2 exposure for short periods (fr...
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creator | Urani, C. Melchioretto, P. Canevali, C. Morazzoni, F. Gribaldo, L. |
description | Cadmium is a widely distributed industrial and environmental pollutant. Principle target organs are soft tissues such as the liver, where cadmium accumulates with a biological half-life of approximately 20–30 years causing a variety of toxic responses. In HepG2, CdCl
2 exposure for short periods (from 1 to 24
h) induces differential expression of stress proteins, including MT and hsp70. However, less is known about the stress response during a prolonged exposure to this metal. MTT assay showed a low cytotoxicity of CdCl
2 (0.1, 0.5, 1, 2, 5, 10
μM), over a period of 72
h. Cadmium uptake by ICP–AES technique and the corresponding expression of stress proteins (MT, hsp70) during the same prolonged time were also analysed. Results show that Cd was continuously and increasingly accumulated, at the highest of the concentrations tested. Metallothionein expression was up-regulated with a saturation curve at 48 as well as 72
h after CdCl
2 exposure. High levels of MT probably confer an acquired tolerance to the stress and protection against cell injury as demonstrated by low cytotoxicity values. On the contrary, the unchanged pattern of hsp70 expression suggests that this protective mechanism, unlike other members of the family, is less involved during CdCl
2 prolonged exposure. |
doi_str_mv | 10.1016/j.tiv.2006.08.014 |
format | Article |
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2 exposure for short periods (from 1 to 24
h) induces differential expression of stress proteins, including MT and hsp70. However, less is known about the stress response during a prolonged exposure to this metal. MTT assay showed a low cytotoxicity of CdCl
2 (0.1, 0.5, 1, 2, 5, 10
μM), over a period of 72
h. Cadmium uptake by ICP–AES technique and the corresponding expression of stress proteins (MT, hsp70) during the same prolonged time were also analysed. Results show that Cd was continuously and increasingly accumulated, at the highest of the concentrations tested. Metallothionein expression was up-regulated with a saturation curve at 48 as well as 72
h after CdCl
2 exposure. High levels of MT probably confer an acquired tolerance to the stress and protection against cell injury as demonstrated by low cytotoxicity values. On the contrary, the unchanged pattern of hsp70 expression suggests that this protective mechanism, unlike other members of the family, is less involved during CdCl
2 prolonged exposure.</description><identifier>ISSN: 0887-2333</identifier><identifier>EISSN: 1879-3177</identifier><identifier>DOI: 10.1016/j.tiv.2006.08.014</identifier><identifier>PMID: 17055695</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Cadmium ; Cadmium Chloride - pharmacokinetics ; Cadmium Chloride - toxicity ; Cell Line, Tumor ; Cell Survival - drug effects ; HepG2 ; Hsp70 ; HSP70 Heat-Shock Proteins - biosynthesis ; Humans ; Liver - drug effects ; Liver - metabolism ; Metallothionein - biosynthesis ; Metallothioneins</subject><ispartof>Toxicology in vitro, 2007-03, Vol.21 (2), p.314-319</ispartof><rights>2006 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-9539a12bc7901d44807c99a5d333ac5be0686443a6fa33d01028600c2ae7a55a3</citedby><cites>FETCH-LOGICAL-c413t-9539a12bc7901d44807c99a5d333ac5be0686443a6fa33d01028600c2ae7a55a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tiv.2006.08.014$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17055695$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Urani, C.</creatorcontrib><creatorcontrib>Melchioretto, P.</creatorcontrib><creatorcontrib>Canevali, C.</creatorcontrib><creatorcontrib>Morazzoni, F.</creatorcontrib><creatorcontrib>Gribaldo, L.</creatorcontrib><title>Metallothionein and hsp70 expression in HepG2 cells after prolonged cadmium exposure</title><title>Toxicology in vitro</title><addtitle>Toxicol In Vitro</addtitle><description>Cadmium is a widely distributed industrial and environmental pollutant. Principle target organs are soft tissues such as the liver, where cadmium accumulates with a biological half-life of approximately 20–30 years causing a variety of toxic responses. In HepG2, CdCl
2 exposure for short periods (from 1 to 24
h) induces differential expression of stress proteins, including MT and hsp70. However, less is known about the stress response during a prolonged exposure to this metal. MTT assay showed a low cytotoxicity of CdCl
2 (0.1, 0.5, 1, 2, 5, 10
μM), over a period of 72
h. Cadmium uptake by ICP–AES technique and the corresponding expression of stress proteins (MT, hsp70) during the same prolonged time were also analysed. Results show that Cd was continuously and increasingly accumulated, at the highest of the concentrations tested. Metallothionein expression was up-regulated with a saturation curve at 48 as well as 72
h after CdCl
2 exposure. High levels of MT probably confer an acquired tolerance to the stress and protection against cell injury as demonstrated by low cytotoxicity values. On the contrary, the unchanged pattern of hsp70 expression suggests that this protective mechanism, unlike other members of the family, is less involved during CdCl
2 prolonged exposure.</description><subject>Cadmium</subject><subject>Cadmium Chloride - pharmacokinetics</subject><subject>Cadmium Chloride - toxicity</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>HepG2</subject><subject>Hsp70</subject><subject>HSP70 Heat-Shock Proteins - biosynthesis</subject><subject>Humans</subject><subject>Liver - drug effects</subject><subject>Liver - metabolism</subject><subject>Metallothionein - biosynthesis</subject><subject>Metallothioneins</subject><issn>0887-2333</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMtKLDEURYNc0fbxAU6kRndW5UlSqSQ4EvEFihMdh3RyWtPUy6RK9O9N0w3O7h0dOKy92SxCzihUFGhzsa6m8FkxgKYCVQGt98iCKqlLTqX8QxaglCwZ5_yQHKW0BgChGByQQypBiEaLBXl5wsm27TC9h6HH0Be298V7GiUU-DVGTCn_i_y_x_GOFQ7bNhV2NWEsxji0Q_-GvnDWd2HuNokhzRFPyP7KtglPd_eYvN7evFzfl4_Pdw_XV4-lqymfSi24tpQtndRAfV0rkE5rK3xebJ1YIjSqqWtum5Xl3AMFphoAxyxKK4Tlx-TvtjdP-ZgxTaYLaTPR9jjMyTBQQjNG_wtS3XChqM4g3YIuDilFXJkxhs7Gb0PBbJybtcnOzca5AWWy85w535XPyw79b2InOQOXWwCzi8-A0SQXsHfoQ0Q3GT-Ef9T_AAdUkS0</recordid><startdate>20070301</startdate><enddate>20070301</enddate><creator>Urani, C.</creator><creator>Melchioretto, P.</creator><creator>Canevali, C.</creator><creator>Morazzoni, F.</creator><creator>Gribaldo, L.</creator><general>Elsevier Ltd</general><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>7U7</scope><scope>C1K</scope></search><sort><creationdate>20070301</creationdate><title>Metallothionein and hsp70 expression in HepG2 cells after prolonged cadmium exposure</title><author>Urani, C. ; Melchioretto, P. ; Canevali, C. ; Morazzoni, F. ; Gribaldo, L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-9539a12bc7901d44807c99a5d333ac5be0686443a6fa33d01028600c2ae7a55a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Cadmium</topic><topic>Cadmium Chloride - pharmacokinetics</topic><topic>Cadmium Chloride - toxicity</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>HepG2</topic><topic>Hsp70</topic><topic>HSP70 Heat-Shock Proteins - biosynthesis</topic><topic>Humans</topic><topic>Liver - drug effects</topic><topic>Liver - metabolism</topic><topic>Metallothionein - biosynthesis</topic><topic>Metallothioneins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Urani, C.</creatorcontrib><creatorcontrib>Melchioretto, P.</creatorcontrib><creatorcontrib>Canevali, C.</creatorcontrib><creatorcontrib>Morazzoni, F.</creatorcontrib><creatorcontrib>Gribaldo, L.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Toxicology in vitro</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Urani, C.</au><au>Melchioretto, P.</au><au>Canevali, C.</au><au>Morazzoni, F.</au><au>Gribaldo, L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metallothionein and hsp70 expression in HepG2 cells after prolonged cadmium exposure</atitle><jtitle>Toxicology in vitro</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2007-03-01</date><risdate>2007</risdate><volume>21</volume><issue>2</issue><spage>314</spage><epage>319</epage><pages>314-319</pages><issn>0887-2333</issn><eissn>1879-3177</eissn><abstract>Cadmium is a widely distributed industrial and environmental pollutant. Principle target organs are soft tissues such as the liver, where cadmium accumulates with a biological half-life of approximately 20–30 years causing a variety of toxic responses. In HepG2, CdCl
2 exposure for short periods (from 1 to 24
h) induces differential expression of stress proteins, including MT and hsp70. However, less is known about the stress response during a prolonged exposure to this metal. MTT assay showed a low cytotoxicity of CdCl
2 (0.1, 0.5, 1, 2, 5, 10
μM), over a period of 72
h. Cadmium uptake by ICP–AES technique and the corresponding expression of stress proteins (MT, hsp70) during the same prolonged time were also analysed. Results show that Cd was continuously and increasingly accumulated, at the highest of the concentrations tested. Metallothionein expression was up-regulated with a saturation curve at 48 as well as 72
h after CdCl
2 exposure. High levels of MT probably confer an acquired tolerance to the stress and protection against cell injury as demonstrated by low cytotoxicity values. On the contrary, the unchanged pattern of hsp70 expression suggests that this protective mechanism, unlike other members of the family, is less involved during CdCl
2 prolonged exposure.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>17055695</pmid><doi>10.1016/j.tiv.2006.08.014</doi><tpages>6</tpages></addata></record> |
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subjects | Cadmium Cadmium Chloride - pharmacokinetics Cadmium Chloride - toxicity Cell Line, Tumor Cell Survival - drug effects HepG2 Hsp70 HSP70 Heat-Shock Proteins - biosynthesis Humans Liver - drug effects Liver - metabolism Metallothionein - biosynthesis Metallothioneins |
title | Metallothionein and hsp70 expression in HepG2 cells after prolonged cadmium exposure |
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