Influence of donor age on vinblastine-induced chromosome malsegregation in cultured peripheral lymphocytes

The incidence of spontaneous aneuploidy in human somatic and germ cells is known to be positively associated with aging. However, the influence of age on the individual susceptibility to chemically induced chromosome malsegregation has not been elucidated. In this study the spindle poison vinblastin...

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Veröffentlicht in:Mutagenesis 2002-01, Vol.17 (1), p.83-88
Hauptverfasser: Leopardi, Paola, Marcon, Francesca, Dobrowolny, Gabriella, Zijno, Andrea, Crebelli, Riccardo
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container_start_page 83
container_title Mutagenesis
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creator Leopardi, Paola
Marcon, Francesca
Dobrowolny, Gabriella
Zijno, Andrea
Crebelli, Riccardo
description The incidence of spontaneous aneuploidy in human somatic and germ cells is known to be positively associated with aging. However, the influence of age on the individual susceptibility to chemically induced chromosome malsegregation has not been elucidated. In this study the spindle poison vinblastine (VBL) was used as a model compound to assess the influence of donor age on chemically induced chromosome malsegregation in cultured lymphocytes. Blood cultures from 20 female donors belonging to two different age groups (10 50 years) were treated with VBL (7.5 ng/ml) from 43 h after mitogen stimulation until harvest at 60 h, i.e. during the time interval corresponding to G2/M. In order to block cytokinesis, cytochalasin B (6 μg/ml) was added to cultures at 44 h. For each donor the incidence of micronuclei, polyploidy and malsegregation (non-disjunction and loss) of chromosomes X and 8 was determined using fluorescence in situ hybridization with chromosome-specific centromeric probes. Both background incidence of micronuclei and spontaneous chromosome X non-disjunction were significantly elevated in older donors. Individual responses to VBL treatment showed wide interindividual variability, which was not significantly associated with the age of the donor. In both age classes chromosome X was more susceptible than chromosome 8 to both spontaneous and VBL-induced malsegregation. These results indicate that donor age has a limited influence on the aneugenic effects exerted by VBL in peripheral lymphocytes in vitro. Other factors have to be considered to account for the large interindividual variation in sensitivity to VBL challenge observed in this work.
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However, the influence of age on the individual susceptibility to chemically induced chromosome malsegregation has not been elucidated. In this study the spindle poison vinblastine (VBL) was used as a model compound to assess the influence of donor age on chemically induced chromosome malsegregation in cultured lymphocytes. Blood cultures from 20 female donors belonging to two different age groups (10 &lt;30 years and 10 &gt;50 years) were treated with VBL (7.5 ng/ml) from 43 h after mitogen stimulation until harvest at 60 h, i.e. during the time interval corresponding to G2/M. In order to block cytokinesis, cytochalasin B (6 μg/ml) was added to cultures at 44 h. For each donor the incidence of micronuclei, polyploidy and malsegregation (non-disjunction and loss) of chromosomes X and 8 was determined using fluorescence in situ hybridization with chromosome-specific centromeric probes. Both background incidence of micronuclei and spontaneous chromosome X non-disjunction were significantly elevated in older donors. Individual responses to VBL treatment showed wide interindividual variability, which was not significantly associated with the age of the donor. In both age classes chromosome X was more susceptible than chromosome 8 to both spontaneous and VBL-induced malsegregation. These results indicate that donor age has a limited influence on the aneugenic effects exerted by VBL in peripheral lymphocytes in vitro. 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However, the influence of age on the individual susceptibility to chemically induced chromosome malsegregation has not been elucidated. In this study the spindle poison vinblastine (VBL) was used as a model compound to assess the influence of donor age on chemically induced chromosome malsegregation in cultured lymphocytes. Blood cultures from 20 female donors belonging to two different age groups (10 &lt;30 years and 10 &gt;50 years) were treated with VBL (7.5 ng/ml) from 43 h after mitogen stimulation until harvest at 60 h, i.e. during the time interval corresponding to G2/M. In order to block cytokinesis, cytochalasin B (6 μg/ml) was added to cultures at 44 h. For each donor the incidence of micronuclei, polyploidy and malsegregation (non-disjunction and loss) of chromosomes X and 8 was determined using fluorescence in situ hybridization with chromosome-specific centromeric probes. Both background incidence of micronuclei and spontaneous chromosome X non-disjunction were significantly elevated in older donors. Individual responses to VBL treatment showed wide interindividual variability, which was not significantly associated with the age of the donor. In both age classes chromosome X was more susceptible than chromosome 8 to both spontaneous and VBL-induced malsegregation. These results indicate that donor age has a limited influence on the aneugenic effects exerted by VBL in peripheral lymphocytes in vitro. Other factors have to be considered to account for the large interindividual variation in sensitivity to VBL challenge observed in this work.</description><subject>Adult</subject><subject>Aging - blood</subject><subject>Aging - genetics</subject><subject>Aging - pathology</subject><subject>Aneuploidy</subject><subject>Biological and medical sciences</subject><subject>Cells, Cultured - drug effects</subject><subject>Cells, Cultured - ultrastructure</subject><subject>Chromosome Segregation - drug effects</subject><subject>Chromosomes, Human - drug effects</subject><subject>Chromosomes, Human, Pair 8 - drug effects</subject><subject>Cytochalasin B - pharmacology</subject><subject>Drug Resistance</subject><subject>Drug toxicity and drugs side effects treatment</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetic Variation</subject><subject>Humans</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Lymphocytes - drug effects</subject><subject>Lymphocytes - ultrastructure</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Micronucleus Tests</subject><subject>Middle Aged</subject><subject>Miscellaneous (drug allergy, mutagens, teratogens...)</subject><subject>Molecular and cellular biology</subject><subject>Molecular genetics</subject><subject>Mutagenesis. Repair</subject><subject>Nondisjunction, Genetic</subject><subject>Pharmacology. Drug treatments</subject><subject>Spindle Apparatus - drug effects</subject><subject>Vinblastine - pharmacology</subject><subject>Vinblastine - toxicity</subject><subject>X Chromosome - drug effects</subject><issn>0267-8357</issn><issn>1464-3804</issn><issn>1464-3804</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpF0M1v1DAQBXALgehSuHJEvsAtW0-c-OOIKmgrrYSEirTqxfI6k10Xxw52gtj_npRd0dMc5vfe4RHyHtgamOZXwzzZPV6BXMNa8RdkBY1oKq5Y85KsWC1kpXgrL8ibUh4ZA1kL9ppcAMi2rrlekce72IcZo0OaetqlmDJdCmmK9LePu2DL5CNWPnazw466Q05DKmlAOthQcJ9xbye_aB-pm8M050WNmP14wGwDDcdhPCR3nLC8Ja_6p8y7870kP75-ub--rTbfbu6uP28q13A2VQ2reeuglU4KBazeIecotLSgVe9apW3XcAHYyZ0WTgMDjrW2suuVtVwrfkk-nXrHnH7NWCYz-OIwBBsxzcWA4qxhQixwfYIup1Iy9mbMfrD5aICZp3XNaV0D0oBRfAl8ODfPuwG7Z36ecwEfz8AWZ0OfbXS-PDsuWtb8K6pOzpcJ__z_2_zTCMlla263D2a7eQB1s7033_lf0JyVDw</recordid><startdate>200201</startdate><enddate>200201</enddate><creator>Leopardi, Paola</creator><creator>Marcon, Francesca</creator><creator>Dobrowolny, Gabriella</creator><creator>Zijno, Andrea</creator><creator>Crebelli, Riccardo</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</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>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>200201</creationdate><title>Influence of donor age on vinblastine-induced chromosome malsegregation in cultured peripheral lymphocytes</title><author>Leopardi, Paola ; Marcon, Francesca ; Dobrowolny, Gabriella ; Zijno, Andrea ; Crebelli, Riccardo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-40235c157c768102be33e697a198fc589ad4361ed7b96c91013e29a7df8aa3983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aging - blood</topic><topic>Aging - genetics</topic><topic>Aging - pathology</topic><topic>Aneuploidy</topic><topic>Biological and medical sciences</topic><topic>Cells, Cultured - drug effects</topic><topic>Cells, Cultured - ultrastructure</topic><topic>Chromosome Segregation - drug effects</topic><topic>Chromosomes, Human - drug effects</topic><topic>Chromosomes, Human, Pair 8 - drug effects</topic><topic>Cytochalasin B - pharmacology</topic><topic>Drug Resistance</topic><topic>Drug toxicity and drugs side effects treatment</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetic Variation</topic><topic>Humans</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Lymphocytes - drug effects</topic><topic>Lymphocytes - ultrastructure</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Micronucleus Tests</topic><topic>Middle Aged</topic><topic>Miscellaneous (drug allergy, mutagens, teratogens...)</topic><topic>Molecular and cellular biology</topic><topic>Molecular genetics</topic><topic>Mutagenesis. Repair</topic><topic>Nondisjunction, Genetic</topic><topic>Pharmacology. Drug treatments</topic><topic>Spindle Apparatus - drug effects</topic><topic>Vinblastine - pharmacology</topic><topic>Vinblastine - toxicity</topic><topic>X Chromosome - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Leopardi, Paola</creatorcontrib><creatorcontrib>Marcon, Francesca</creatorcontrib><creatorcontrib>Dobrowolny, Gabriella</creatorcontrib><creatorcontrib>Zijno, Andrea</creatorcontrib><creatorcontrib>Crebelli, Riccardo</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><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>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><jtitle>Mutagenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Leopardi, Paola</au><au>Marcon, Francesca</au><au>Dobrowolny, Gabriella</au><au>Zijno, Andrea</au><au>Crebelli, Riccardo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of donor age on vinblastine-induced chromosome malsegregation in cultured peripheral lymphocytes</atitle><jtitle>Mutagenesis</jtitle><addtitle>Mutagenesis</addtitle><date>2002-01</date><risdate>2002</risdate><volume>17</volume><issue>1</issue><spage>83</spage><epage>88</epage><pages>83-88</pages><issn>0267-8357</issn><issn>1464-3804</issn><eissn>1464-3804</eissn><coden>MUTAEX</coden><abstract>The incidence of spontaneous aneuploidy in human somatic and germ cells is known to be positively associated with aging. However, the influence of age on the individual susceptibility to chemically induced chromosome malsegregation has not been elucidated. In this study the spindle poison vinblastine (VBL) was used as a model compound to assess the influence of donor age on chemically induced chromosome malsegregation in cultured lymphocytes. Blood cultures from 20 female donors belonging to two different age groups (10 &lt;30 years and 10 &gt;50 years) were treated with VBL (7.5 ng/ml) from 43 h after mitogen stimulation until harvest at 60 h, i.e. during the time interval corresponding to G2/M. In order to block cytokinesis, cytochalasin B (6 μg/ml) was added to cultures at 44 h. For each donor the incidence of micronuclei, polyploidy and malsegregation (non-disjunction and loss) of chromosomes X and 8 was determined using fluorescence in situ hybridization with chromosome-specific centromeric probes. Both background incidence of micronuclei and spontaneous chromosome X non-disjunction were significantly elevated in older donors. Individual responses to VBL treatment showed wide interindividual variability, which was not significantly associated with the age of the donor. In both age classes chromosome X was more susceptible than chromosome 8 to both spontaneous and VBL-induced malsegregation. These results indicate that donor age has a limited influence on the aneugenic effects exerted by VBL in peripheral lymphocytes in vitro. Other factors have to be considered to account for the large interindividual variation in sensitivity to VBL challenge observed in this work.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>11752239</pmid><doi>10.1093/mutage/17.1.83</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aging - blood
Aging - genetics
Aging - pathology
Aneuploidy
Biological and medical sciences
Cells, Cultured - drug effects
Cells, Cultured - ultrastructure
Chromosome Segregation - drug effects
Chromosomes, Human - drug effects
Chromosomes, Human, Pair 8 - drug effects
Cytochalasin B - pharmacology
Drug Resistance
Drug toxicity and drugs side effects treatment
Female
Fundamental and applied biological sciences. Psychology
Genetic Variation
Humans
In Situ Hybridization, Fluorescence
Lymphocytes - drug effects
Lymphocytes - ultrastructure
Male
Medical sciences
Micronucleus Tests
Middle Aged
Miscellaneous (drug allergy, mutagens, teratogens...)
Molecular and cellular biology
Molecular genetics
Mutagenesis. Repair
Nondisjunction, Genetic
Pharmacology. Drug treatments
Spindle Apparatus - drug effects
Vinblastine - pharmacology
Vinblastine - toxicity
X Chromosome - drug effects
title Influence of donor age on vinblastine-induced chromosome malsegregation in cultured peripheral lymphocytes
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