Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons
Autophagy is an essential cellular degradation pathway in neurons; defects in autophagy are sufficient to induce neurodegeneration. In this paper, we investigate autophagosome dynamics in primary dorsal root ganglion neurons. Autophagosome biogenesis occurs distally in a constitutive process at the...
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Veröffentlicht in: | The Journal of cell biology 2012-02, Vol.196 (4), p.407-417 |
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description | Autophagy is an essential cellular degradation pathway in neurons; defects in autophagy are sufficient to induce neurodegeneration. In this paper, we investigate autophagosome dynamics in primary dorsal root ganglion neurons. Autophagosome biogenesis occurs distally in a constitutive process at the neurite tip. Autophagosomes initially move bidirectionally and then switch to unidirectional, processive movement toward the cell soma driven by dynein. Autophagosomes copurify with anterograde and retrograde motors, suggesting that the activity of bound kinesin motors is effectively down-regulated to yield robust retrograde motility driven by dynein. Both organelle and soluble cargoes are internalized into autophagosomes, including mitochondria and ubiquitin. As autophagosomes move distally to proximally, they undergo maturation and become increasingly acidified, consistent with the formation of an autolysosomal compartment that may more efficiently degrade cargo. This maturation is accompanied by a switch to bidirectional motility characteristic of lysosomes. Together, autophagosome biogenesis and maturation in primary neurons is a constitutive process that is spatially and temporally regulated along the axon. |
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In this paper, we investigate autophagosome dynamics in primary dorsal root ganglion neurons. Autophagosome biogenesis occurs distally in a constitutive process at the neurite tip. Autophagosomes initially move bidirectionally and then switch to unidirectional, processive movement toward the cell soma driven by dynein. Autophagosomes copurify with anterograde and retrograde motors, suggesting that the activity of bound kinesin motors is effectively down-regulated to yield robust retrograde motility driven by dynein. Both organelle and soluble cargoes are internalized into autophagosomes, including mitochondria and ubiquitin. As autophagosomes move distally to proximally, they undergo maturation and become increasingly acidified, consistent with the formation of an autolysosomal compartment that may more efficiently degrade cargo. This maturation is accompanied by a switch to bidirectional motility characteristic of lysosomes. 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In this paper, we investigate autophagosome dynamics in primary dorsal root ganglion neurons. Autophagosome biogenesis occurs distally in a constitutive process at the neurite tip. Autophagosomes initially move bidirectionally and then switch to unidirectional, processive movement toward the cell soma driven by dynein. Autophagosomes copurify with anterograde and retrograde motors, suggesting that the activity of bound kinesin motors is effectively down-regulated to yield robust retrograde motility driven by dynein. Both organelle and soluble cargoes are internalized into autophagosomes, including mitochondria and ubiquitin. As autophagosomes move distally to proximally, they undergo maturation and become increasingly acidified, consistent with the formation of an autolysosomal compartment that may more efficiently degrade cargo. This maturation is accompanied by a switch to bidirectional motility characteristic of lysosomes. Together, autophagosome biogenesis and maturation in primary neurons is a constitutive process that is spatially and temporally regulated along the axon.</description><subject>Animals</subject><subject>Autophagy</subject><subject>Axons - physiology</subject><subject>Biological Transport</subject><subject>Biosynthesis</subject><subject>Cell Compartmentation</subject><subject>Cellular biology</subject><subject>Dyneins - metabolism</subject><subject>Fluorescent Antibody Technique</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Image Processing, Computer-Assisted</subject><subject>Maturation</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Motility</subject><subject>Neurodegeneration</subject><subject>Neurons</subject><subject>Neurons - cytology</subject><subject>Neurons - metabolism</subject><subject>Phagosomes - physiology</subject><subject>Superoxide Dismutase - physiology</subject><subject>Superoxide Dismutase-1</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFvFCEUh4nR2LV69GqIF71M5QHDDBeTpmnVpIkXPZM3DLPLZgZWYDT976V23agHuZDAly-_936EvAR2AawX7_Z2uOAMgCng7BHZQCtZ04Nkj8mGMQ6Nbnl7Rp7lvGeMyU6Kp-SMcyGgl3JDxsu1xMMOtzHHxWXqgy8ei6OjzwXn-Y5iGOmCZU31bU0-bGlJGPIhpkJL_IFppGXnqHXzTKsDq4Iekl8w3dHg1hRDfk6eTDhn9-J4n5OvN9dfrj42t58_fLq6vG1sC7w0na0HNaLUzo2da_WIoHjPRztZqQaNGlqllbAda3mHWuIkYZhAuXZgAsQ5ef_gPazD4kbrQo06m2MaE9Gbv3-C35lt_G4E74XWvAreHAUpfltdLmbx-X4yDC6u2WjOOyUYyEq-_S8JgoueM_kr1et_0H1cU6iLqD4lQTDVVah5gGyKOSc3nVIDM_dFm1q0ORVd-Vd_jnqifzcrfgIwC6YQ</recordid><startdate>20120220</startdate><enddate>20120220</enddate><creator>Maday, Sandra</creator><creator>Wallace, Karen E</creator><creator>Holzbaur, Erika L F</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120220</creationdate><title>Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons</title><author>Maday, Sandra ; Wallace, Karen E ; Holzbaur, Erika L F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-7cccca9aa49eed7e59da16282dcfc46b9a9156963c70527a94af41bf16e5b0313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Autophagy</topic><topic>Axons - physiology</topic><topic>Biological Transport</topic><topic>Biosynthesis</topic><topic>Cell Compartmentation</topic><topic>Cellular biology</topic><topic>Dyneins - metabolism</topic><topic>Fluorescent Antibody Technique</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Image Processing, Computer-Assisted</topic><topic>Maturation</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Motility</topic><topic>Neurodegeneration</topic><topic>Neurons</topic><topic>Neurons - cytology</topic><topic>Neurons - metabolism</topic><topic>Phagosomes - physiology</topic><topic>Superoxide Dismutase - physiology</topic><topic>Superoxide Dismutase-1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Maday, Sandra</creatorcontrib><creatorcontrib>Wallace, Karen E</creatorcontrib><creatorcontrib>Holzbaur, Erika L F</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Maday, Sandra</au><au>Wallace, Karen E</au><au>Holzbaur, Erika L F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>2012-02-20</date><risdate>2012</risdate><volume>196</volume><issue>4</issue><spage>407</spage><epage>417</epage><pages>407-417</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>Autophagy is an essential cellular degradation pathway in neurons; defects in autophagy are sufficient to induce neurodegeneration. In this paper, we investigate autophagosome dynamics in primary dorsal root ganglion neurons. Autophagosome biogenesis occurs distally in a constitutive process at the neurite tip. Autophagosomes initially move bidirectionally and then switch to unidirectional, processive movement toward the cell soma driven by dynein. Autophagosomes copurify with anterograde and retrograde motors, suggesting that the activity of bound kinesin motors is effectively down-regulated to yield robust retrograde motility driven by dynein. Both organelle and soluble cargoes are internalized into autophagosomes, including mitochondria and ubiquitin. As autophagosomes move distally to proximally, they undergo maturation and become increasingly acidified, consistent with the formation of an autolysosomal compartment that may more efficiently degrade cargo. This maturation is accompanied by a switch to bidirectional motility characteristic of lysosomes. Together, autophagosome biogenesis and maturation in primary neurons is a constitutive process that is spatially and temporally regulated along the axon.</abstract><cop>United States</cop><pub>Rockefeller University Press</pub><pmid>22331844</pmid><doi>10.1083/jcb.201106120</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Autophagy Axons - physiology Biological Transport Biosynthesis Cell Compartmentation Cellular biology Dyneins - metabolism Fluorescent Antibody Technique Green Fluorescent Proteins - metabolism Image Processing, Computer-Assisted Maturation Mice Mice, Transgenic Motility Neurodegeneration Neurons Neurons - cytology Neurons - metabolism Phagosomes - physiology Superoxide Dismutase - physiology Superoxide Dismutase-1 |
title | Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons |
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