A new experimental protocol as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic assay to assess the haematotoxic potential of new drugs
In this work, a first attempt to set-up a new in vitro experimental protocol with culture in liquid medium and flow cytometry analysis of bone marrow progenitors is described. This protocol is proposed as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic in vitro a...
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Veröffentlicht in: | Toxicology (Amsterdam) 2006-08, Vol.20 (5), p.750-756 |
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creator | Dal Negro, Gianni Vandin, Luca Bonato, Monica Repeto, Paolo Sciuscio, Davide |
description | In this work, a first attempt to set-up a new in vitro experimental protocol with culture in liquid medium and flow cytometry analysis of bone marrow progenitors is described. This protocol is proposed as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic in vitro assay currently used to assess the toxic potential of new drugs in the bone marrow. This new experimental approach should enable to speed up the procedure of the in vitro haematotoxic potential assessment, to reduce inter-experimental variability and to enhance result accuracy. Preliminary results obtained demonstrated that the progenitor cell count by flow cytometry replacing the light microscopy granulocyte/macrophage colony count represents a tremendous improvement in terms of accuracy and standardisation. Moreover, differential counts of cell sub-populations can be performed by using specific monoclonal antibodies. Furthermore, this method demonstrated to be time-saving, since 4
day cell incubation period is required instead of 7–14
day incubation in the CFU-GM clonogenic assay. On the basis of results obtained so far, the new experimental protocol proposed looks a promising alternative to the CFU-GM clonogenic assay currently used. |
doi_str_mv | 10.1016/j.tiv.2005.10.015 |
format | Article |
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day cell incubation period is required instead of 7–14
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day cell incubation period is required instead of 7–14
day incubation in the CFU-GM clonogenic assay. On the basis of results obtained so far, the new experimental protocol proposed looks a promising alternative to the CFU-GM clonogenic assay currently used.</description><subject>Animals</subject><subject>Bone marrow</subject><subject>Cell Lineage</subject><subject>Colony-forming unit-granulocyte/macrophages</subject><subject>Colony-Forming Units Assay - methods</subject><subject>Culture Media</subject><subject>Doxorubicin - toxicity</subject><subject>Flow Cytometry</subject><subject>Granulocytes - drug effects</subject><subject>Granulocytes - physiology</subject><subject>Hematopoietic Stem Cells - drug effects</subject><subject>In vitro</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - physiology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Inbred DBA</subject><subject>Monoclonal antibodies</subject><subject>Zidovudine - toxicity</subject><issn>0887-2333</issn><issn>0300-483X</issn><issn>1879-3177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhi0EotvCD-CCfEJwyNYfm9gRp2pFW6QiLvRsee1J1qvEDrbTdn8TfxLvh8SNk-3xO8_MvIPQB0qWlNDmerfM7mnJCKnLe0lo_QotqBRtxakQr9GCSCkqxjm_QJcp7UgRSkbeogvacEZXrVygPzfYwzOGlwmiG8FnPeAphhxMGLBOWHushwzR61IKcA44bwGXz-D3VRfi6HyPZ-9y1Uft5yGYfYbrUZsYpq3uAX9e3z5Wdz--YFNSQg_emcJNen9glQukdERuNYw6l8IvRTCFXFpxpZfQHfuzce7TO_Sm00OC9-fzCj3efvu1vq8eft59X988VIZLlisrrLWbjaU1txQos4xqsHUDgmw6w0zNxMq2q5q03LbCSmZl1zSiWUlr67pkXaFPJ24x4vcMKavRJQPDoD2EOSnatryRvClCehKWaVOK0KmpmKjjXlGiDhtSO1VsU4cNHULkCP94hs-bEey_jPNKiuDrSQBlxCcHUSXjwBuwLoLJygb3H_xfJFylhQ</recordid><startdate>20060801</startdate><enddate>20060801</enddate><creator>Dal Negro, Gianni</creator><creator>Vandin, Luca</creator><creator>Bonato, Monica</creator><creator>Repeto, Paolo</creator><creator>Sciuscio, Davide</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20060801</creationdate><title>A new experimental protocol as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic assay to assess the haematotoxic potential of new drugs</title><author>Dal Negro, Gianni ; Vandin, Luca ; Bonato, Monica ; Repeto, Paolo ; Sciuscio, Davide</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c382t-d7dddbbd153d1e12d21aed56e70bfc2c5274d945093d97d82d8f667648dd55153</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Bone marrow</topic><topic>Cell Lineage</topic><topic>Colony-forming unit-granulocyte/macrophages</topic><topic>Colony-Forming Units Assay - methods</topic><topic>Culture Media</topic><topic>Doxorubicin - toxicity</topic><topic>Flow Cytometry</topic><topic>Granulocytes - drug effects</topic><topic>Granulocytes - physiology</topic><topic>Hematopoietic Stem Cells - drug effects</topic><topic>In vitro</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - physiology</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Inbred DBA</topic><topic>Monoclonal antibodies</topic><topic>Zidovudine - toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dal Negro, Gianni</creatorcontrib><creatorcontrib>Vandin, Luca</creatorcontrib><creatorcontrib>Bonato, Monica</creatorcontrib><creatorcontrib>Repeto, Paolo</creatorcontrib><creatorcontrib>Sciuscio, Davide</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</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><jtitle>Toxicology (Amsterdam)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dal Negro, Gianni</au><au>Vandin, Luca</au><au>Bonato, Monica</au><au>Repeto, Paolo</au><au>Sciuscio, Davide</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A new experimental protocol as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic assay to assess the haematotoxic potential of new drugs</atitle><jtitle>Toxicology (Amsterdam)</jtitle><addtitle>Toxicol In Vitro</addtitle><date>2006-08-01</date><risdate>2006</risdate><volume>20</volume><issue>5</issue><spage>750</spage><epage>756</epage><pages>750-756</pages><issn>0887-2333</issn><issn>0300-483X</issn><eissn>1879-3177</eissn><abstract>In this work, a first attempt to set-up a new in vitro experimental protocol with culture in liquid medium and flow cytometry analysis of bone marrow progenitors is described. This protocol is proposed as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic in vitro assay currently used to assess the toxic potential of new drugs in the bone marrow. This new experimental approach should enable to speed up the procedure of the in vitro haematotoxic potential assessment, to reduce inter-experimental variability and to enhance result accuracy. Preliminary results obtained demonstrated that the progenitor cell count by flow cytometry replacing the light microscopy granulocyte/macrophage colony count represents a tremendous improvement in terms of accuracy and standardisation. Moreover, differential counts of cell sub-populations can be performed by using specific monoclonal antibodies. Furthermore, this method demonstrated to be time-saving, since 4
day cell incubation period is required instead of 7–14
day incubation in the CFU-GM clonogenic assay. On the basis of results obtained so far, the new experimental protocol proposed looks a promising alternative to the CFU-GM clonogenic assay currently used.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>16321498</pmid><doi>10.1016/j.tiv.2005.10.015</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Bone marrow Cell Lineage Colony-forming unit-granulocyte/macrophages Colony-Forming Units Assay - methods Culture Media Doxorubicin - toxicity Flow Cytometry Granulocytes - drug effects Granulocytes - physiology Hematopoietic Stem Cells - drug effects In vitro Macrophages - drug effects Macrophages - physiology Male Mice Mice, Inbred C57BL Mice, Inbred DBA Monoclonal antibodies Zidovudine - toxicity |
title | A new experimental protocol as an alternative to the colony-forming unit-granulocyte/macrophage (CFU-GM) clonogenic assay to assess the haematotoxic potential of new drugs |
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