Electron Probe X-Ray Microanalysis of Residual Bodies in Aged Cultured Human Glial Cells
Secondary lysosomes of the residual body type are frequent in nondividing cells from phase III cultures of human glial cells. These organelles have previously been shown to be analogous to lipofuscin granules of postmitotic cells in vivo. Most recent studies favor the assumption that residual bodies...
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description | Secondary lysosomes of the residual body type are frequent in nondividing cells from phase III cultures of human glial cells. These organelles have previously been shown to be analogous to lipofuscin granules of postmitotic cells in vivo. Most recent studies favor the assumption that residual bodies mainly result from incomplete degradation within the lysosomal vacuome of endogenous cellular components such as mitochondria and endoplasmic reticulum. Since iron occurs in several metalloenzymes produced by such organelles, it should then be possible to demonstrate accumulated iron within residual bodies. X-ray dispersive analysis of sectioned biological material is often hampered by diffusion and dissolution during preparation, as well as by too low a concentration of the elements. In this study we cultured glial cells on Formvar-coated gold grids and studied them unsectioned, after brief glutaraldehyde fixation and freeze-drying, in a transmission electron microscope at 100 kV in TEM and STEM mode. It was then possible to demonstrate iron in residual bodies of aged cells, presumably because the type of preparation utilized does not permit much dissolution. |
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These organelles have previously been shown to be analogous to lipofuscin granules of postmitotic cells in vivo. Most recent studies favor the assumption that residual bodies mainly result from incomplete degradation within the lysosomal vacuome of endogenous cellular components such as mitochondria and endoplasmic reticulum. Since iron occurs in several metalloenzymes produced by such organelles, it should then be possible to demonstrate accumulated iron within residual bodies. X-ray dispersive analysis of sectioned biological material is often hampered by diffusion and dissolution during preparation, as well as by too low a concentration of the elements. In this study we cultured glial cells on Formvar-coated gold grids and studied them unsectioned, after brief glutaraldehyde fixation and freeze-drying, in a transmission electron microscope at 100 kV in TEM and STEM mode. 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Pathol.; (United States)</title><addtitle>Ultrastruct Pathol</addtitle><description>Secondary lysosomes of the residual body type are frequent in nondividing cells from phase III cultures of human glial cells. These organelles have previously been shown to be analogous to lipofuscin granules of postmitotic cells in vivo. Most recent studies favor the assumption that residual bodies mainly result from incomplete degradation within the lysosomal vacuome of endogenous cellular components such as mitochondria and endoplasmic reticulum. Since iron occurs in several metalloenzymes produced by such organelles, it should then be possible to demonstrate accumulated iron within residual bodies. X-ray dispersive analysis of sectioned biological material is often hampered by diffusion and dissolution during preparation, as well as by too low a concentration of the elements. In this study we cultured glial cells on Formvar-coated gold grids and studied them unsectioned, after brief glutaraldehyde fixation and freeze-drying, in a transmission electron microscope at 100 kV in TEM and STEM mode. It was then possible to demonstrate iron in residual bodies of aged cells, presumably because the type of preparation utilized does not permit much dissolution.</description><subject>550200 - Biochemistry</subject><subject>550300 - Cytology</subject><subject>AGING</subject><subject>aging in vitro</subject><subject>BASIC BIOLOGICAL SCIENCES</subject><subject>BIOCHEMISTRY</subject><subject>CELL CONSTITUENTS</subject><subject>CELL CULTURES</subject><subject>Cell Nucleus - ultrastructure</subject><subject>Cells, Cultured</subject><subject>CHEMICAL ANALYSIS</subject><subject>CHEMISTRY</subject><subject>cultured human glial cells</subject><subject>CYTOCHEMISTRY</subject><subject>DISEASES</subject><subject>DISSOLUTION</subject><subject>ELECTRON MICROPROBE ANALYSIS</subject><subject>ELECTRON MICROSCOPY</subject><subject>Electron Probe Microanalysis</subject><subject>ELEMENTS</subject><subject>Endoplasmic Reticulum - ultrastructure</subject><subject>ENZYME ACTIVITY</subject><subject>GLIOMAS</subject><subject>Humans</subject><subject>IRON</subject><subject>LYSOSOMES</subject><subject>Lysosomes - ultrastructure</subject><subject>METALS</subject><subject>MICROANALYSIS</subject><subject>MICROSCOPY</subject><subject>Mitochondria - ultrastructure</subject><subject>NEOPLASMS</subject><subject>NONDESTRUCTIVE ANALYSIS</subject><subject>ORGANOIDS</subject><subject>TRANSITION ELEMENTS</subject><subject>TRANSMISSION ELECTRON MICROSCOPY</subject><subject>X-ray dispersive analysis</subject><subject>X-RAY EMISSION ANALYSIS</subject><issn>0191-3123</issn><issn>1521-0758</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UUuLFDEQDqKs4-oP8CAED95aU3lMp9HLOqy7woqyKOwtpJNqJ0u6s5t0I_PvzTiDIKJ1qYLvQdVXhDwH9loA694w6EAA14x1IEF08ICsQHFoWKv0Q7La400liMfkSSm3jDElmD4hJy0XQrV8RW7OI7o5p4l-yalHetNc2x39FFxOdrJxV0KhaaDXWIJfbKTvkw9YaJjo2Xf0dLPEecl1uFxGO9GLGCpngzGWp-TRYGPBZ8d-Sr59OP-6uWyuPl983JxdNU5yPTdoa3ktOfoOnPSylz2Xg9a6G9a6B-XRysHLjqOq1QvN3RosA--ZxpaJU_Ly4JvKHExxYUa3dWma6llGtWLdQltJrw6ku5zuFyyzGUNxdU07YVqKaZUCxX65wYFY7y8l42Duchht3hlgZh-5-SvyqnlxNF_6Ef1vxTHjir874GEaUh7tj5SjN7PdxZSHbCcXyt763_Zv_5Bv0cZ562xGc5uWXJ9U_rPcT7Jpn6w</recordid><startdate>1980</startdate><enddate>1980</enddate><creator>Blomquist, E.</creator><creator>Fredriksson, B.-A.</creator><creator>Brunk, U.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</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>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>1980</creationdate><title>Electron Probe X-Ray Microanalysis of Residual Bodies in Aged Cultured Human Glial Cells</title><author>Blomquist, E. ; Fredriksson, B.-A. ; Brunk, U.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-eaaaad842ed91c4d4b4b24f8889f68b15dea4fd492e5555b382c61a01dd08e703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>550200 - Biochemistry</topic><topic>550300 - Cytology</topic><topic>AGING</topic><topic>aging in vitro</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>BIOCHEMISTRY</topic><topic>CELL CONSTITUENTS</topic><topic>CELL CULTURES</topic><topic>Cell Nucleus - ultrastructure</topic><topic>Cells, Cultured</topic><topic>CHEMICAL ANALYSIS</topic><topic>CHEMISTRY</topic><topic>cultured human glial cells</topic><topic>CYTOCHEMISTRY</topic><topic>DISEASES</topic><topic>DISSOLUTION</topic><topic>ELECTRON MICROPROBE ANALYSIS</topic><topic>ELECTRON MICROSCOPY</topic><topic>Electron Probe Microanalysis</topic><topic>ELEMENTS</topic><topic>Endoplasmic Reticulum - ultrastructure</topic><topic>ENZYME ACTIVITY</topic><topic>GLIOMAS</topic><topic>Humans</topic><topic>IRON</topic><topic>LYSOSOMES</topic><topic>Lysosomes - ultrastructure</topic><topic>METALS</topic><topic>MICROANALYSIS</topic><topic>MICROSCOPY</topic><topic>Mitochondria - ultrastructure</topic><topic>NEOPLASMS</topic><topic>NONDESTRUCTIVE ANALYSIS</topic><topic>ORGANOIDS</topic><topic>TRANSITION ELEMENTS</topic><topic>TRANSMISSION ELECTRON MICROSCOPY</topic><topic>X-ray dispersive analysis</topic><topic>X-RAY EMISSION ANALYSIS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Blomquist, E.</creatorcontrib><creatorcontrib>Fredriksson, B.-A.</creatorcontrib><creatorcontrib>Brunk, U.</creatorcontrib><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><collection>OSTI.GOV</collection><jtitle>Ultrastruct. Pathol.; (United States)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Blomquist, E.</au><au>Fredriksson, B.-A.</au><au>Brunk, U.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electron Probe X-Ray Microanalysis of Residual Bodies in Aged Cultured Human Glial Cells</atitle><jtitle>Ultrastruct. Pathol.; (United States)</jtitle><addtitle>Ultrastruct Pathol</addtitle><date>1980</date><risdate>1980</risdate><volume>1</volume><issue>1</issue><spage>11</spage><epage>17</epage><pages>11-17</pages><issn>0191-3123</issn><eissn>1521-0758</eissn><abstract>Secondary lysosomes of the residual body type are frequent in nondividing cells from phase III cultures of human glial cells. These organelles have previously been shown to be analogous to lipofuscin granules of postmitotic cells in vivo. Most recent studies favor the assumption that residual bodies mainly result from incomplete degradation within the lysosomal vacuome of endogenous cellular components such as mitochondria and endoplasmic reticulum. Since iron occurs in several metalloenzymes produced by such organelles, it should then be possible to demonstrate accumulated iron within residual bodies. X-ray dispersive analysis of sectioned biological material is often hampered by diffusion and dissolution during preparation, as well as by too low a concentration of the elements. In this study we cultured glial cells on Formvar-coated gold grids and studied them unsectioned, after brief glutaraldehyde fixation and freeze-drying, in a transmission electron microscope at 100 kV in TEM and STEM mode. It was then possible to demonstrate iron in residual bodies of aged cells, presumably because the type of preparation utilized does not permit much dissolution.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>7233572</pmid><doi>10.3109/01913128009141391</doi><tpages>7</tpages></addata></record> |
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subjects | 550200 - Biochemistry 550300 - Cytology AGING aging in vitro BASIC BIOLOGICAL SCIENCES BIOCHEMISTRY CELL CONSTITUENTS CELL CULTURES Cell Nucleus - ultrastructure Cells, Cultured CHEMICAL ANALYSIS CHEMISTRY cultured human glial cells CYTOCHEMISTRY DISEASES DISSOLUTION ELECTRON MICROPROBE ANALYSIS ELECTRON MICROSCOPY Electron Probe Microanalysis ELEMENTS Endoplasmic Reticulum - ultrastructure ENZYME ACTIVITY GLIOMAS Humans IRON LYSOSOMES Lysosomes - ultrastructure METALS MICROANALYSIS MICROSCOPY Mitochondria - ultrastructure NEOPLASMS NONDESTRUCTIVE ANALYSIS ORGANOIDS TRANSITION ELEMENTS TRANSMISSION ELECTRON MICROSCOPY X-ray dispersive analysis X-RAY EMISSION ANALYSIS |
title | Electron Probe X-Ray Microanalysis of Residual Bodies in Aged Cultured Human Glial Cells |
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