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Axonal spheroids in neurodegeneration
Axonal spheroids are bubble-like biological features that form on most degenerating axons, yet little is known about their influence on degenerative processes. Their formation and growth has been observed in response to various degenerative triggers such as injury, oxidative stress, inflammatory fac...
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Published in: | Molecular and cellular neuroscience 2021-12, Vol.117, p.103679-103679, Article 103679 |
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description | Axonal spheroids are bubble-like biological features that form on most degenerating axons, yet little is known about their influence on degenerative processes. Their formation and growth has been observed in response to various degenerative triggers such as injury, oxidative stress, inflammatory factors, and neurotoxic molecules. They often contain cytoskeletal elements and organelles, and, depending on the pathological insult, can colocalize with disease-related proteins such as amyloid precursor protein (APP), ubiquitin, and motor proteins. Initial formation of axonal spheroids depends on the disruption of axonal and membrane tension governed by cytoskeleton structure and calcium levels. Shortly after spheroid formation, the engulfment signal phosphatidylserine (PS) is exposed on the outer leaflet of spheroid plasma membrane, suggesting an important role for axonal spheroids in phagocytosis and debris clearance during degeneration. Spheroids can grow until they rupture, allowing pro-degenerative factors to exit the axon into extracellular space and accelerating neurodegeneration. Though much remains to be discovered in this area, axonal spheroid research promises to lend insight into the etiologies of neurodegenerative disease, and may be an important target for therapeutic intervention. This review summarizes over 100 years of work, describing what is known about axonal spheroid structure, regulation and function.
•Axonal spheroids accumulate disease-associated proteins, organelles, and cytoskeletal elements .•Axonal cytoskeleton rearrangements and membrane rupture cause influx of ions like calcium, promoting spheroid formation and growth.•Spheroids can recruit phagocytes via phosphatidylserine, indicating a potential role for spheroids in cellular waste elimination.•Spheroid contents can activate pro-degeneration receptors and known degeneration pathways. |
doi_str_mv | 10.1016/j.mcn.2021.103679 |
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•Axonal spheroids accumulate disease-associated proteins, organelles, and cytoskeletal elements .•Axonal cytoskeleton rearrangements and membrane rupture cause influx of ions like calcium, promoting spheroid formation and growth.•Spheroids can recruit phagocytes via phosphatidylserine, indicating a potential role for spheroids in cellular waste elimination.•Spheroid contents can activate pro-degeneration receptors and known degeneration pathways.</description><identifier>ISSN: 1044-7431</identifier><identifier>EISSN: 1095-9327</identifier><identifier>DOI: 10.1016/j.mcn.2021.103679</identifier><identifier>PMID: 34678457</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Axonal spheroids ; Axons ; Cytoskeleton ; Degeneration ; Humans ; Neurodegenerative disease ; Neurodegenerative Diseases</subject><ispartof>Molecular and cellular neuroscience, 2021-12, Vol.117, p.103679-103679, Article 103679</ispartof><rights>2021 Elsevier Inc.</rights><rights>Copyright © 2021 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c451t-f6fc19140912314dfc18ae00d853e835b558dd4b13576622124e4256babfd7553</citedby><cites>FETCH-LOGICAL-c451t-f6fc19140912314dfc18ae00d853e835b558dd4b13576622124e4256babfd7553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,777,781,882,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34678457$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yong, Yu</creatorcontrib><creatorcontrib>Hunter-Chang, Sarah</creatorcontrib><creatorcontrib>Stepanova, Ekaterina</creatorcontrib><creatorcontrib>Deppmann, Christopher</creatorcontrib><title>Axonal spheroids in neurodegeneration</title><title>Molecular and cellular neuroscience</title><addtitle>Mol Cell Neurosci</addtitle><description>Axonal spheroids are bubble-like biological features that form on most degenerating axons, yet little is known about their influence on degenerative processes. Their formation and growth has been observed in response to various degenerative triggers such as injury, oxidative stress, inflammatory factors, and neurotoxic molecules. They often contain cytoskeletal elements and organelles, and, depending on the pathological insult, can colocalize with disease-related proteins such as amyloid precursor protein (APP), ubiquitin, and motor proteins. Initial formation of axonal spheroids depends on the disruption of axonal and membrane tension governed by cytoskeleton structure and calcium levels. Shortly after spheroid formation, the engulfment signal phosphatidylserine (PS) is exposed on the outer leaflet of spheroid plasma membrane, suggesting an important role for axonal spheroids in phagocytosis and debris clearance during degeneration. Spheroids can grow until they rupture, allowing pro-degenerative factors to exit the axon into extracellular space and accelerating neurodegeneration. Though much remains to be discovered in this area, axonal spheroid research promises to lend insight into the etiologies of neurodegenerative disease, and may be an important target for therapeutic intervention. This review summarizes over 100 years of work, describing what is known about axonal spheroid structure, regulation and function.
•Axonal spheroids accumulate disease-associated proteins, organelles, and cytoskeletal elements .•Axonal cytoskeleton rearrangements and membrane rupture cause influx of ions like calcium, promoting spheroid formation and growth.•Spheroids can recruit phagocytes via phosphatidylserine, indicating a potential role for spheroids in cellular waste elimination.•Spheroid contents can activate pro-degeneration receptors and known degeneration pathways.</description><subject>Axonal spheroids</subject><subject>Axons</subject><subject>Cytoskeleton</subject><subject>Degeneration</subject><subject>Humans</subject><subject>Neurodegenerative disease</subject><subject>Neurodegenerative Diseases</subject><issn>1044-7431</issn><issn>1095-9327</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LAzEQhoMoVqs_wIv04nFrvrOLIJTiFxS86Dlkk9k2pU1Ksi36792yWvTiaWaY932HeRC6InhMMJG3y_HahjHFlHQzk6o6QmcEV6KoGFXH-57zQnFGBug85yXGWNCKnaIB41KVXKgzdDP5iMGsRnmzgBS9yyMfRgG2KTqYQ4BkWh_DBTppzCrD5XcdovfHh7fpczF7fXqZTmaF5YK0RSMbSyrCcUUoI9x1U2kAY1cKBiUTtRClc7wmTCgpKSWUA6dC1qZunBKCDdF9n7vZ1mtwFkKbzEpvkl-b9Kmj8frvJviFnsedLhWnpVJdAOkDbIo5J2gOXoL1nple6o6Z3jPTPbPOc_376MHxA6kT3PUC6F7feUg6Ww_BgvMJbKtd9P_EfwEhWnx3</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Yong, Yu</creator><creator>Hunter-Chang, Sarah</creator><creator>Stepanova, Ekaterina</creator><creator>Deppmann, Christopher</creator><general>Elsevier Inc</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>5PM</scope></search><sort><creationdate>20211201</creationdate><title>Axonal spheroids in neurodegeneration</title><author>Yong, Yu ; Hunter-Chang, Sarah ; Stepanova, Ekaterina ; Deppmann, Christopher</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c451t-f6fc19140912314dfc18ae00d853e835b558dd4b13576622124e4256babfd7553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Axonal spheroids</topic><topic>Axons</topic><topic>Cytoskeleton</topic><topic>Degeneration</topic><topic>Humans</topic><topic>Neurodegenerative disease</topic><topic>Neurodegenerative Diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yong, Yu</creatorcontrib><creatorcontrib>Hunter-Chang, Sarah</creatorcontrib><creatorcontrib>Stepanova, Ekaterina</creatorcontrib><creatorcontrib>Deppmann, Christopher</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular and cellular neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yong, Yu</au><au>Hunter-Chang, Sarah</au><au>Stepanova, Ekaterina</au><au>Deppmann, Christopher</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Axonal spheroids in neurodegeneration</atitle><jtitle>Molecular and cellular neuroscience</jtitle><addtitle>Mol Cell Neurosci</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>117</volume><spage>103679</spage><epage>103679</epage><pages>103679-103679</pages><artnum>103679</artnum><issn>1044-7431</issn><eissn>1095-9327</eissn><abstract>Axonal spheroids are bubble-like biological features that form on most degenerating axons, yet little is known about their influence on degenerative processes. Their formation and growth has been observed in response to various degenerative triggers such as injury, oxidative stress, inflammatory factors, and neurotoxic molecules. They often contain cytoskeletal elements and organelles, and, depending on the pathological insult, can colocalize with disease-related proteins such as amyloid precursor protein (APP), ubiquitin, and motor proteins. Initial formation of axonal spheroids depends on the disruption of axonal and membrane tension governed by cytoskeleton structure and calcium levels. Shortly after spheroid formation, the engulfment signal phosphatidylserine (PS) is exposed on the outer leaflet of spheroid plasma membrane, suggesting an important role for axonal spheroids in phagocytosis and debris clearance during degeneration. Spheroids can grow until they rupture, allowing pro-degenerative factors to exit the axon into extracellular space and accelerating neurodegeneration. Though much remains to be discovered in this area, axonal spheroid research promises to lend insight into the etiologies of neurodegenerative disease, and may be an important target for therapeutic intervention. This review summarizes over 100 years of work, describing what is known about axonal spheroid structure, regulation and function.
•Axonal spheroids accumulate disease-associated proteins, organelles, and cytoskeletal elements .•Axonal cytoskeleton rearrangements and membrane rupture cause influx of ions like calcium, promoting spheroid formation and growth.•Spheroids can recruit phagocytes via phosphatidylserine, indicating a potential role for spheroids in cellular waste elimination.•Spheroid contents can activate pro-degeneration receptors and known degeneration pathways.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>34678457</pmid><doi>10.1016/j.mcn.2021.103679</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Axonal spheroids Axons Cytoskeleton Degeneration Humans Neurodegenerative disease Neurodegenerative Diseases |
title | Axonal spheroids in neurodegeneration |
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