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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Veröffentlicht in:Ultrastruct. Pathol.; (United States) 1980, Vol.1 (1), p.11-17
Hauptverfasser: Blomquist, E., Fredriksson, B.-A., Brunk, U.
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container_title Ultrastruct. Pathol.; (United States)
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Fredriksson, B.-A.
Brunk, U.
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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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. 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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 &amp; 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. 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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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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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