Respiration characteristics of mitochondria in parental and giant transformed cells of the murine Nemeth-Kellner lymphoma
Respiration characteristics of mitochondria of the parental and giant cells of murine NK/Ly (Nemeth—Kellner lymphoma) were studied. The giant cell‐enriched ascites were obtained by serial intraperitoneal injections of vinblastine in tumour‐bearing mice. Ascites containing >70% giant cells were us...
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Veröffentlicht in: | Cell biology international 2012-01, Vol.36 (1), p.71-77 |
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description | Respiration characteristics of mitochondria of the parental and giant cells of murine NK/Ly (Nemeth—Kellner lymphoma) were studied. The giant cell‐enriched ascites were obtained by serial intraperitoneal injections of vinblastine in tumour‐bearing mice. Ascites containing >70% giant cells were used. Their diameter of was over 17 μm (∼2800 μm3), while the diameter of the parental cells was 12.7 μm (1100 μm3). The respiration rate of mitochondria in situ was measured by oxygen consumption in intact and digitonin‐permeabilized NK/Ly cells. Endogenous respiration of intact giant NK/Ly cells was three times higher compared to the parental ones, roughly in agreement with the volume change. The giant NK/Ly cells were far more resistant to permeabilization with digitonin than the parental cells, as shown by Trypan Blue and LDH (lactate dehydrogenase) release tests. After digitonin permeabilization, oxygen consumption was reduced to a minimal level (0.06 ng atom O/(s × 106 cells) in both types of cells. Addition of α‐ketoglutarate or succinate to the incubation medium increased oxygen consumption in the parental cells by 46 and 164% respectively. In the giant NK/Ly cells, the corresponding increases were 164 and 276%. Addition of ADP to α‐ketoglutarate‐ or succinate‐supplemented medium further stimulated oxygen consumption of the permeabilized NK/Ly cells; however, the effect of ADP was more pronounced in the giant cells. In addition, indices of respiratory control were significantly higher in the giant cells. Oligomycin suppressed considerably the respiration of the intact giant cells but had a much weaker effect on parental cells. Thus, giant NK/Ly cells possess much higher respiration rates and show tighter coupling between the respiration and oxidative phosphorylation compared with parental cells. |
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The giant cell‐enriched ascites were obtained by serial intraperitoneal injections of vinblastine in tumour‐bearing mice. Ascites containing >70% giant cells were used. Their diameter of was over 17 μm (∼2800 μm3), while the diameter of the parental cells was 12.7 μm (1100 μm3). The respiration rate of mitochondria in situ was measured by oxygen consumption in intact and digitonin‐permeabilized NK/Ly cells. Endogenous respiration of intact giant NK/Ly cells was three times higher compared to the parental ones, roughly in agreement with the volume change. The giant NK/Ly cells were far more resistant to permeabilization with digitonin than the parental cells, as shown by Trypan Blue and LDH (lactate dehydrogenase) release tests. After digitonin permeabilization, oxygen consumption was reduced to a minimal level (0.06 ng atom O/(s × 106 cells) in both types of cells. Addition of α‐ketoglutarate or succinate to the incubation medium increased oxygen consumption in the parental cells by 46 and 164% respectively. In the giant NK/Ly cells, the corresponding increases were 164 and 276%. Addition of ADP to α‐ketoglutarate‐ or succinate‐supplemented medium further stimulated oxygen consumption of the permeabilized NK/Ly cells; however, the effect of ADP was more pronounced in the giant cells. In addition, indices of respiratory control were significantly higher in the giant cells. Oligomycin suppressed considerably the respiration of the intact giant cells but had a much weaker effect on parental cells. Thus, giant NK/Ly cells possess much higher respiration rates and show tighter coupling between the respiration and oxidative phosphorylation compared with parental cells.</description><identifier>ISSN: 1065-6995</identifier><identifier>EISSN: 1095-8355</identifier><identifier>DOI: 10.1042/CBI20110017</identifier><identifier>PMID: 21899518</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adenosine Diphosphate - pharmacology ; Animals ; Cell Line, Tumor ; Cell Membrane Permeability ; Cell Size ; Digitonin - pharmacology ; giant cell transformation ; Giant Cells - drug effects ; Giant Cells - metabolism ; Ketoglutaric Acids - pharmacology ; L-Lactate Dehydrogenase - metabolism ; Lymphoma - metabolism ; Lymphoma - pathology ; membrane permeability ; Mice ; Mice, Inbred C57BL ; Mitochondria - drug effects ; Mitochondria - metabolism ; mitochondrial respiration ; murine Nemeth-Kellner lymphoma (NK/Ly) ; Oligomycins - pharmacology ; Oxidative Phosphorylation ; Oxygen Consumption - drug effects ; Respiration - drug effects ; vinblastine ; Vinblastine - pharmacology</subject><ispartof>Cell biology international, 2012-01, Vol.36 (1), p.71-77</ispartof><rights>The Author(s) Journal compilation © 2012 International Federation for Cell Biology</rights><rights>The Author(s) Journal compilation © 2012 Portland Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3689-d6fe833df0c36fbe9b1d8a4572e4c5ae9a2e096b3c1930395e3f8d32770691793</citedby><cites>FETCH-LOGICAL-c3689-d6fe833df0c36fbe9b1d8a4572e4c5ae9a2e096b3c1930395e3f8d32770691793</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1042%2FCBI20110017$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1042%2FCBI20110017$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21899518$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Horbay, Rostyslav O.</creatorcontrib><creatorcontrib>Manko, Bohdan O.</creatorcontrib><creatorcontrib>Manko, Volodymyr V.</creatorcontrib><creatorcontrib>Lootsik, Maxim D.</creatorcontrib><creatorcontrib>Stoika, Rostyslav S.</creatorcontrib><title>Respiration characteristics of mitochondria in parental and giant transformed cells of the murine Nemeth-Kellner lymphoma</title><title>Cell biology international</title><addtitle>Cell Biol Int</addtitle><description>Respiration characteristics of mitochondria of the parental and giant cells of murine NK/Ly (Nemeth—Kellner lymphoma) were studied. The giant cell‐enriched ascites were obtained by serial intraperitoneal injections of vinblastine in tumour‐bearing mice. Ascites containing >70% giant cells were used. Their diameter of was over 17 μm (∼2800 μm3), while the diameter of the parental cells was 12.7 μm (1100 μm3). The respiration rate of mitochondria in situ was measured by oxygen consumption in intact and digitonin‐permeabilized NK/Ly cells. Endogenous respiration of intact giant NK/Ly cells was three times higher compared to the parental ones, roughly in agreement with the volume change. The giant NK/Ly cells were far more resistant to permeabilization with digitonin than the parental cells, as shown by Trypan Blue and LDH (lactate dehydrogenase) release tests. After digitonin permeabilization, oxygen consumption was reduced to a minimal level (0.06 ng atom O/(s × 106 cells) in both types of cells. Addition of α‐ketoglutarate or succinate to the incubation medium increased oxygen consumption in the parental cells by 46 and 164% respectively. In the giant NK/Ly cells, the corresponding increases were 164 and 276%. Addition of ADP to α‐ketoglutarate‐ or succinate‐supplemented medium further stimulated oxygen consumption of the permeabilized NK/Ly cells; however, the effect of ADP was more pronounced in the giant cells. In addition, indices of respiratory control were significantly higher in the giant cells. Oligomycin suppressed considerably the respiration of the intact giant cells but had a much weaker effect on parental cells. Thus, giant NK/Ly cells possess much higher respiration rates and show tighter coupling between the respiration and oxidative phosphorylation compared with parental cells.</description><subject>Adenosine Diphosphate - pharmacology</subject><subject>Animals</subject><subject>Cell Line, Tumor</subject><subject>Cell Membrane Permeability</subject><subject>Cell Size</subject><subject>Digitonin - pharmacology</subject><subject>giant cell transformation</subject><subject>Giant Cells - drug effects</subject><subject>Giant Cells - metabolism</subject><subject>Ketoglutaric Acids - pharmacology</subject><subject>L-Lactate Dehydrogenase - metabolism</subject><subject>Lymphoma - metabolism</subject><subject>Lymphoma - pathology</subject><subject>membrane permeability</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>mitochondrial respiration</subject><subject>murine Nemeth-Kellner lymphoma (NK/Ly)</subject><subject>Oligomycins - pharmacology</subject><subject>Oxidative Phosphorylation</subject><subject>Oxygen Consumption - drug effects</subject><subject>Respiration - drug effects</subject><subject>vinblastine</subject><subject>Vinblastine - pharmacology</subject><issn>1065-6995</issn><issn>1095-8355</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc1v1DAQxa0K1JbSE3fkGwcU8Eec2EdYQSlUi6BU7c3yOpPGJbGD7RXsf4_DlooTJ4_Hv_c084zQM0peUVKz16u354xQSghtD9AxJUpUkgvxaKkbUTVKiSP0JKW7QtBaNofoiFFZulQeo91XSLOLJrvgsR1MNDZDdCk7m3Do8eRysEPwXXQGO49nE8FnM2LjO3zrjM84R-NTH-IEHbYwjn90eQA8baPzgNcwQR6qT-XJQ8TjbpqHMJmn6HFvxgSn9-cJunr_7tvqQ3Xx-ex89eaisryRquqaHiTnXU_Kvd-A2tBOmlq0DGorDCjDgKhmwy1VnHAlgPey46xtSaNoq_gJerH3nWP4sYWU9eTSMqfxELZJK6KYVLyWhXy5J20MKUXo9RzdZOJOU6KXqPU_URf6-b3vdlNWf2D_ZlsAugd-uhF2__Na6jWjbBm22mvKD8CvB42J33XT8lbo6_WZvvwov9wwdqnX_De785iG</recordid><startdate>201201</startdate><enddate>201201</enddate><creator>Horbay, Rostyslav O.</creator><creator>Manko, Bohdan O.</creator><creator>Manko, Volodymyr V.</creator><creator>Lootsik, Maxim D.</creator><creator>Stoika, Rostyslav S.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>201201</creationdate><title>Respiration characteristics of mitochondria in parental and giant transformed cells of the murine Nemeth-Kellner lymphoma</title><author>Horbay, Rostyslav O. ; Manko, Bohdan O. ; Manko, Volodymyr V. ; Lootsik, Maxim D. ; Stoika, Rostyslav S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3689-d6fe833df0c36fbe9b1d8a4572e4c5ae9a2e096b3c1930395e3f8d32770691793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adenosine Diphosphate - pharmacology</topic><topic>Animals</topic><topic>Cell Line, Tumor</topic><topic>Cell Membrane Permeability</topic><topic>Cell Size</topic><topic>Digitonin - pharmacology</topic><topic>giant cell transformation</topic><topic>Giant Cells - drug effects</topic><topic>Giant Cells - metabolism</topic><topic>Ketoglutaric Acids - pharmacology</topic><topic>L-Lactate Dehydrogenase - metabolism</topic><topic>Lymphoma - metabolism</topic><topic>Lymphoma - pathology</topic><topic>membrane permeability</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>mitochondrial respiration</topic><topic>murine Nemeth-Kellner lymphoma (NK/Ly)</topic><topic>Oligomycins - pharmacology</topic><topic>Oxidative Phosphorylation</topic><topic>Oxygen Consumption - drug effects</topic><topic>Respiration - drug effects</topic><topic>vinblastine</topic><topic>Vinblastine - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Horbay, Rostyslav O.</creatorcontrib><creatorcontrib>Manko, Bohdan O.</creatorcontrib><creatorcontrib>Manko, Volodymyr V.</creatorcontrib><creatorcontrib>Lootsik, Maxim D.</creatorcontrib><creatorcontrib>Stoika, Rostyslav S.</creatorcontrib><collection>Istex</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>Cell biology international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Horbay, Rostyslav O.</au><au>Manko, Bohdan O.</au><au>Manko, Volodymyr V.</au><au>Lootsik, Maxim D.</au><au>Stoika, Rostyslav S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Respiration characteristics of mitochondria in parental and giant transformed cells of the murine Nemeth-Kellner lymphoma</atitle><jtitle>Cell biology international</jtitle><addtitle>Cell Biol Int</addtitle><date>2012-01</date><risdate>2012</risdate><volume>36</volume><issue>1</issue><spage>71</spage><epage>77</epage><pages>71-77</pages><issn>1065-6995</issn><eissn>1095-8355</eissn><abstract>Respiration characteristics of mitochondria of the parental and giant cells of murine NK/Ly (Nemeth—Kellner lymphoma) were studied. The giant cell‐enriched ascites were obtained by serial intraperitoneal injections of vinblastine in tumour‐bearing mice. Ascites containing >70% giant cells were used. Their diameter of was over 17 μm (∼2800 μm3), while the diameter of the parental cells was 12.7 μm (1100 μm3). The respiration rate of mitochondria in situ was measured by oxygen consumption in intact and digitonin‐permeabilized NK/Ly cells. Endogenous respiration of intact giant NK/Ly cells was three times higher compared to the parental ones, roughly in agreement with the volume change. The giant NK/Ly cells were far more resistant to permeabilization with digitonin than the parental cells, as shown by Trypan Blue and LDH (lactate dehydrogenase) release tests. After digitonin permeabilization, oxygen consumption was reduced to a minimal level (0.06 ng atom O/(s × 106 cells) in both types of cells. Addition of α‐ketoglutarate or succinate to the incubation medium increased oxygen consumption in the parental cells by 46 and 164% respectively. In the giant NK/Ly cells, the corresponding increases were 164 and 276%. Addition of ADP to α‐ketoglutarate‐ or succinate‐supplemented medium further stimulated oxygen consumption of the permeabilized NK/Ly cells; however, the effect of ADP was more pronounced in the giant cells. In addition, indices of respiratory control were significantly higher in the giant cells. Oligomycin suppressed considerably the respiration of the intact giant cells but had a much weaker effect on parental cells. Thus, giant NK/Ly cells possess much higher respiration rates and show tighter coupling between the respiration and oxidative phosphorylation compared with parental cells.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21899518</pmid><doi>10.1042/CBI20110017</doi><tpages>7</tpages></addata></record> |
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subjects | Adenosine Diphosphate - pharmacology Animals Cell Line, Tumor Cell Membrane Permeability Cell Size Digitonin - pharmacology giant cell transformation Giant Cells - drug effects Giant Cells - metabolism Ketoglutaric Acids - pharmacology L-Lactate Dehydrogenase - metabolism Lymphoma - metabolism Lymphoma - pathology membrane permeability Mice Mice, Inbred C57BL Mitochondria - drug effects Mitochondria - metabolism mitochondrial respiration murine Nemeth-Kellner lymphoma (NK/Ly) Oligomycins - pharmacology Oxidative Phosphorylation Oxygen Consumption - drug effects Respiration - drug effects vinblastine Vinblastine - pharmacology |
title | Respiration characteristics of mitochondria in parental and giant transformed cells of the murine Nemeth-Kellner lymphoma |
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