Organellar clusters formed by mitochondrial‐rough endoplasmic reticulum associations: An ordered arrangement of mitochondria in hepatocytes
Our objective was to determine if mitochondrial‐rough endoplasmic reticulum (mt‐RER) associations provide for an ordered arrangement of mitochondria in the cell. If such an ordered arrangement exists, it might be manifested by grouping of mitochondria according to size and biochemical properties. Li...
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Veröffentlicht in: | Hepatology (Baltimore, Md.) Md.), 1995-09, Vol.22 (3), p.837-846 |
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description | Our objective was to determine if mitochondrial‐rough endoplasmic reticulum (mt‐RER) associations provide for an ordered arrangement of mitochondria in the cell. If such an ordered arrangement exists, it might be manifested by grouping of mitochondria according to size and biochemical properties. Liver homogenate was subjected to rate zonal centrifugation for fractionating mitochondrial clusters. These clusters were then examined for morphological and biochemical characteristics. Scanning electron microscopy (SEM) showed that (1) mitochondria were held together in clusters by rough endoplasmic reticulum, (2) clusters consisted of mitochondria of comparable size, and (3) a 45‐fold difference in average mitochondrial volume existed between the organelles of the fastest and slowest sedimenting clusters. Transmission electron microscopy (TEM) affirmed that all of the organellar clusters examined were mitochondria associated with rough endoplasmic reticulum. Cytochrome oxidase and mitochondrial DNA were found to be proportional to mitochondrial volume, indicating that these components were synthesized in proportion to increases in volume. Conversely, succinic dehydrogenase and ornithine carbamoyl transferase were increased disproportionately (2.9‐fold and six‐fold, respectively) with increase in mitochondrial volume. It is evident from this biochemical heterogeneity that clusters composed of larger mitochondria differ functionally from clusters of smaller mitochondria. The size‐ordered arrangement suggests that this organization is in some way related to the biogenesis of hepatocyte mitochondria. It is also conjectured that the biochemical heterogeneity is a consequence of addition of selected proteins (e.g., succinic dehydrogenase and carbamoyl transferase) to mitochondria in a developmental process as they mature into larger organelles. (Hepatology 1995; 22:837–846.) |
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If such an ordered arrangement exists, it might be manifested by grouping of mitochondria according to size and biochemical properties. Liver homogenate was subjected to rate zonal centrifugation for fractionating mitochondrial clusters. These clusters were then examined for morphological and biochemical characteristics. Scanning electron microscopy (SEM) showed that (1) mitochondria were held together in clusters by rough endoplasmic reticulum, (2) clusters consisted of mitochondria of comparable size, and (3) a 45‐fold difference in average mitochondrial volume existed between the organelles of the fastest and slowest sedimenting clusters. Transmission electron microscopy (TEM) affirmed that all of the organellar clusters examined were mitochondria associated with rough endoplasmic reticulum. Cytochrome oxidase and mitochondrial DNA were found to be proportional to mitochondrial volume, indicating that these components were synthesized in proportion to increases in volume. Conversely, succinic dehydrogenase and ornithine carbamoyl transferase were increased disproportionately (2.9‐fold and six‐fold, respectively) with increase in mitochondrial volume. It is evident from this biochemical heterogeneity that clusters composed of larger mitochondria differ functionally from clusters of smaller mitochondria. The size‐ordered arrangement suggests that this organization is in some way related to the biogenesis of hepatocyte mitochondria. It is also conjectured that the biochemical heterogeneity is a consequence of addition of selected proteins (e.g., succinic dehydrogenase and carbamoyl transferase) to mitochondria in a developmental process as they mature into larger organelles. (Hepatology 1995; 22:837–846.)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.1840220323</identifier><identifier>PMID: 7657291</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Philadelphia, PA: W.B. Saunders</publisher><subject>Animals ; Biological and medical sciences ; Cell structures and functions ; DNA, Mitochondrial - metabolism ; Electron Transport Complex IV - metabolism ; Endoplasmic Reticulum - physiology ; Endoplasmic Reticulum - ultrastructure ; Fundamental and applied biological sciences. Psychology ; Liver - cytology ; Liver - physiology ; Male ; Microscopy, Electron ; Microscopy, Electron, Scanning ; Mitochondria and cell respiration ; Mitochondria, Liver - enzymology ; Mitochondria, Liver - physiology ; Mitochondria, Liver - ultrastructure ; Molecular and cellular biology ; Organelles - physiology ; Organelles - ultrastructure ; Ornithine Carbamoyltransferase - metabolism ; Rats ; Rats, Wistar ; Succinate Dehydrogenase - metabolism</subject><ispartof>Hepatology (Baltimore, Md.), 1995-09, Vol.22 (3), p.837-846</ispartof><rights>Copyright © 1995 American Association for the Study of Liver Diseases</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2963-af7b2d422046f3c57c58686ea7a26cb8136aac3aeaf6c96410f0e17d80fee7e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.1840220323$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.1840220323$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27933,27934,45583,45584</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3657386$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7657291$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cascarano, Joseph</creatorcontrib><creatorcontrib>Chambers, Patricia A.</creatorcontrib><creatorcontrib>Schwartz, Eileen</creatorcontrib><creatorcontrib>Poorkaj, Parvoneh</creatorcontrib><creatorcontrib>Gondo, Roy E.</creatorcontrib><title>Organellar clusters formed by mitochondrial‐rough endoplasmic reticulum associations: An ordered arrangement of mitochondria in hepatocytes</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Our objective was to determine if mitochondrial‐rough endoplasmic reticulum (mt‐RER) associations provide for an ordered arrangement of mitochondria in the cell. If such an ordered arrangement exists, it might be manifested by grouping of mitochondria according to size and biochemical properties. Liver homogenate was subjected to rate zonal centrifugation for fractionating mitochondrial clusters. These clusters were then examined for morphological and biochemical characteristics. Scanning electron microscopy (SEM) showed that (1) mitochondria were held together in clusters by rough endoplasmic reticulum, (2) clusters consisted of mitochondria of comparable size, and (3) a 45‐fold difference in average mitochondrial volume existed between the organelles of the fastest and slowest sedimenting clusters. Transmission electron microscopy (TEM) affirmed that all of the organellar clusters examined were mitochondria associated with rough endoplasmic reticulum. Cytochrome oxidase and mitochondrial DNA were found to be proportional to mitochondrial volume, indicating that these components were synthesized in proportion to increases in volume. Conversely, succinic dehydrogenase and ornithine carbamoyl transferase were increased disproportionately (2.9‐fold and six‐fold, respectively) with increase in mitochondrial volume. It is evident from this biochemical heterogeneity that clusters composed of larger mitochondria differ functionally from clusters of smaller mitochondria. The size‐ordered arrangement suggests that this organization is in some way related to the biogenesis of hepatocyte mitochondria. It is also conjectured that the biochemical heterogeneity is a consequence of addition of selected proteins (e.g., succinic dehydrogenase and carbamoyl transferase) to mitochondria in a developmental process as they mature into larger organelles. (Hepatology 1995; 22:837–846.)</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell structures and functions</subject><subject>DNA, Mitochondrial - metabolism</subject><subject>Electron Transport Complex IV - metabolism</subject><subject>Endoplasmic Reticulum - physiology</subject><subject>Endoplasmic Reticulum - ultrastructure</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Liver - cytology</subject><subject>Liver - physiology</subject><subject>Male</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Electron, Scanning</subject><subject>Mitochondria and cell respiration</subject><subject>Mitochondria, Liver - enzymology</subject><subject>Mitochondria, Liver - physiology</subject><subject>Mitochondria, Liver - ultrastructure</subject><subject>Molecular and cellular biology</subject><subject>Organelles - physiology</subject><subject>Organelles - ultrastructure</subject><subject>Ornithine Carbamoyltransferase - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Succinate Dehydrogenase - metabolism</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkL9uFDEQhy1EFI5AS4fkAqXbw3927V26KAoEKVJSJPVqzju-M_Lah72r6DpeACnPyJPg050CVFQjeT7_ZuYj5B1nS86Y-LjB7ZK3NROCSSFfkAVvhK6kbNhLsmBCs6rjsntFXuf8jTHW1aI9JadaNVp0fEF-3qY1BPQeEjV-zhOmTG1MIw50taOjm6LZxDAkB_7Xj6cU5_WGYhji1kMenaEJJ2dmP48Uco7GweRiyJ_oRaAxDZhKDqQEYY0jholG-08mdYGWC6C87CbMb8iJBZ_x7bGekYfPV_eX19XN7Zevlxc3lRGdkhVYvRJDXU6ulZWm0aZpVasQNAhlVi2XCsBIQLDKdKrmzDLkemiZRdRYyzNyfsjdpvh9xjz1o8tmbyFgnHOvdd12rd6DywNoUsw5oe23yY2Qdj1n_d5_X7bv__gvH94fk-dVcfiMH4WX_odjH7IBb4sZ4_IzJgsmW1Ww7oA9Oo-7_wztr6_u_lrhN-B0o7M</recordid><startdate>199509</startdate><enddate>199509</enddate><creator>Cascarano, Joseph</creator><creator>Chambers, Patricia A.</creator><creator>Schwartz, Eileen</creator><creator>Poorkaj, Parvoneh</creator><creator>Gondo, Roy E.</creator><general>W.B. Saunders</general><general>Wiley</general><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>7X8</scope></search><sort><creationdate>199509</creationdate><title>Organellar clusters formed by mitochondrial‐rough endoplasmic reticulum associations: An ordered arrangement of mitochondria in hepatocytes</title><author>Cascarano, Joseph ; Chambers, Patricia A. ; Schwartz, Eileen ; Poorkaj, Parvoneh ; Gondo, Roy E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2963-af7b2d422046f3c57c58686ea7a26cb8136aac3aeaf6c96410f0e17d80fee7e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell structures and functions</topic><topic>DNA, Mitochondrial - metabolism</topic><topic>Electron Transport Complex IV - metabolism</topic><topic>Endoplasmic Reticulum - physiology</topic><topic>Endoplasmic Reticulum - ultrastructure</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Liver - cytology</topic><topic>Liver - physiology</topic><topic>Male</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Electron, Scanning</topic><topic>Mitochondria and cell respiration</topic><topic>Mitochondria, Liver - enzymology</topic><topic>Mitochondria, Liver - physiology</topic><topic>Mitochondria, Liver - ultrastructure</topic><topic>Molecular and cellular biology</topic><topic>Organelles - physiology</topic><topic>Organelles - ultrastructure</topic><topic>Ornithine Carbamoyltransferase - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Succinate Dehydrogenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cascarano, Joseph</creatorcontrib><creatorcontrib>Chambers, Patricia A.</creatorcontrib><creatorcontrib>Schwartz, Eileen</creatorcontrib><creatorcontrib>Poorkaj, Parvoneh</creatorcontrib><creatorcontrib>Gondo, Roy E.</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cascarano, Joseph</au><au>Chambers, Patricia A.</au><au>Schwartz, Eileen</au><au>Poorkaj, Parvoneh</au><au>Gondo, Roy E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Organellar clusters formed by mitochondrial‐rough endoplasmic reticulum associations: An ordered arrangement of mitochondria in hepatocytes</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>1995-09</date><risdate>1995</risdate><volume>22</volume><issue>3</issue><spage>837</spage><epage>846</epage><pages>837-846</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>Our objective was to determine if mitochondrial‐rough endoplasmic reticulum (mt‐RER) associations provide for an ordered arrangement of mitochondria in the cell. If such an ordered arrangement exists, it might be manifested by grouping of mitochondria according to size and biochemical properties. Liver homogenate was subjected to rate zonal centrifugation for fractionating mitochondrial clusters. These clusters were then examined for morphological and biochemical characteristics. Scanning electron microscopy (SEM) showed that (1) mitochondria were held together in clusters by rough endoplasmic reticulum, (2) clusters consisted of mitochondria of comparable size, and (3) a 45‐fold difference in average mitochondrial volume existed between the organelles of the fastest and slowest sedimenting clusters. Transmission electron microscopy (TEM) affirmed that all of the organellar clusters examined were mitochondria associated with rough endoplasmic reticulum. Cytochrome oxidase and mitochondrial DNA were found to be proportional to mitochondrial volume, indicating that these components were synthesized in proportion to increases in volume. Conversely, succinic dehydrogenase and ornithine carbamoyl transferase were increased disproportionately (2.9‐fold and six‐fold, respectively) with increase in mitochondrial volume. It is evident from this biochemical heterogeneity that clusters composed of larger mitochondria differ functionally from clusters of smaller mitochondria. The size‐ordered arrangement suggests that this organization is in some way related to the biogenesis of hepatocyte mitochondria. It is also conjectured that the biochemical heterogeneity is a consequence of addition of selected proteins (e.g., succinic dehydrogenase and carbamoyl transferase) to mitochondria in a developmental process as they mature into larger organelles. (Hepatology 1995; 22:837–846.)</abstract><cop>Philadelphia, PA</cop><pub>W.B. Saunders</pub><pmid>7657291</pmid><doi>10.1002/hep.1840220323</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences Cell structures and functions DNA, Mitochondrial - metabolism Electron Transport Complex IV - metabolism Endoplasmic Reticulum - physiology Endoplasmic Reticulum - ultrastructure Fundamental and applied biological sciences. Psychology Liver - cytology Liver - physiology Male Microscopy, Electron Microscopy, Electron, Scanning Mitochondria and cell respiration Mitochondria, Liver - enzymology Mitochondria, Liver - physiology Mitochondria, Liver - ultrastructure Molecular and cellular biology Organelles - physiology Organelles - ultrastructure Ornithine Carbamoyltransferase - metabolism Rats Rats, Wistar Succinate Dehydrogenase - metabolism |
title | Organellar clusters formed by mitochondrial‐rough endoplasmic reticulum associations: An ordered arrangement of mitochondria in hepatocytes |
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