Dissociation of Axonal Neurofilament Content from Its Transport Rate
The axonal cytoskeleton of neurofilament (NF) is a long-lived network of fibrous elements believed to be a stationary structure maintained by a small pool of transported cytoskeletal precursors. Accordingly, it may be predicted that NF content in axons can vary independently from the transport rate...
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description | The axonal cytoskeleton of neurofilament (NF) is a long-lived network of fibrous elements believed to be a stationary structure maintained by a small pool of transported cytoskeletal precursors. Accordingly, it may be predicted that NF content in axons can vary independently from the transport rate of NF. In the present report, we confirm this prediction by showing that human NFH transgenic mice and transgenic mice expressing human NFL Ser55 (Asp) develop nearly identical abnormal patterns of NF accumulation and distribution in association with opposite changes in NF slow transport rates. We also show that the rate of NF transport in wild-type mice remains constant along a length of the optic axon where NF content varies 3-fold. Moreover, knockout mice lacking NFH develop even more extreme (6-fold) proximal to distal variation in NF number, which is associated with a normal wild-type rate of NF transport. The independence of regional NF content and NF transport is consistent with previous evidence suggesting that the rate of incorporation of transported NF precursors into a metabolically stable stationary cytoskeletal network is the major determinant of axonal NF content, enabling the generation of the striking local variations in NF number seen along axons. |
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Accordingly, it may be predicted that NF content in axons can vary independently from the transport rate of NF. In the present report, we confirm this prediction by showing that human NFH transgenic mice and transgenic mice expressing human NFL Ser55 (Asp) develop nearly identical abnormal patterns of NF accumulation and distribution in association with opposite changes in NF slow transport rates. We also show that the rate of NF transport in wild-type mice remains constant along a length of the optic axon where NF content varies 3-fold. Moreover, knockout mice lacking NFH develop even more extreme (6-fold) proximal to distal variation in NF number, which is associated with a normal wild-type rate of NF transport. The independence of regional NF content and NF transport is consistent with previous evidence suggesting that the rate of incorporation of transported NF precursors into a metabolically stable stationary cytoskeletal network is the major determinant of axonal NF content, enabling the generation of the striking local variations in NF number seen along axons.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0133848</identifier><identifier>PMID: 26208164</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Animals ; Axonal Transport ; Axons ; Axons - metabolism ; Biology ; Cytoskeleton ; Dementia ; Dissociation ; Female ; Genetic engineering ; Humans ; Immunoglobulins ; Intermediate Filaments - metabolism ; Laboratory animals ; Male ; Medicine ; Mice ; Mice, Knockout ; Mice, Transgenic ; Neurochemistry ; Neurosciences ; Optic Nerve - metabolism ; Phosphatase ; Phosphorylation ; Population ; Predictions ; Proteins ; Psychiatry ; Rodents ; Transgenic mice ; Transport rate</subject><ispartof>PloS one, 2015-07, Vol.10 (7), p.e0133848-e0133848</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Yuan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Yuan et al 2015 Yuan et al</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-8006903a16f70cb85ab1e6f1401e8974c8308637312b8aa77a20f358a4eea3e43</citedby><cites>FETCH-LOGICAL-c692t-8006903a16f70cb85ab1e6f1401e8974c8308637312b8aa77a20f358a4eea3e43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514674/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514674/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,862,883,2098,2917,23849,27907,27908,53774,53776,79351,79352</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26208164$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Reddy, Hemachandra</contributor><creatorcontrib>Yuan, Aidong</creatorcontrib><creatorcontrib>Hassinger, Linda</creatorcontrib><creatorcontrib>Rao, Mala V</creatorcontrib><creatorcontrib>Julien, Jean-Pierre</creatorcontrib><creatorcontrib>Miller, Christopher C J</creatorcontrib><creatorcontrib>Nixon, Ralph A</creatorcontrib><title>Dissociation of Axonal Neurofilament Content from Its Transport Rate</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>The axonal cytoskeleton of neurofilament (NF) is a long-lived network of fibrous elements believed to be a stationary structure maintained by a small pool of transported cytoskeletal precursors. Accordingly, it may be predicted that NF content in axons can vary independently from the transport rate of NF. In the present report, we confirm this prediction by showing that human NFH transgenic mice and transgenic mice expressing human NFL Ser55 (Asp) develop nearly identical abnormal patterns of NF accumulation and distribution in association with opposite changes in NF slow transport rates. We also show that the rate of NF transport in wild-type mice remains constant along a length of the optic axon where NF content varies 3-fold. Moreover, knockout mice lacking NFH develop even more extreme (6-fold) proximal to distal variation in NF number, which is associated with a normal wild-type rate of NF transport. The independence of regional NF content and NF transport is consistent with previous evidence suggesting that the rate of incorporation of transported NF precursors into a metabolically stable stationary cytoskeletal network is the major determinant of axonal NF content, enabling the generation of the striking local variations in NF number seen along axons.</description><subject>Animals</subject><subject>Axonal Transport</subject><subject>Axons</subject><subject>Axons - metabolism</subject><subject>Biology</subject><subject>Cytoskeleton</subject><subject>Dementia</subject><subject>Dissociation</subject><subject>Female</subject><subject>Genetic engineering</subject><subject>Humans</subject><subject>Immunoglobulins</subject><subject>Intermediate Filaments - metabolism</subject><subject>Laboratory animals</subject><subject>Male</subject><subject>Medicine</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Neurochemistry</subject><subject>Neurosciences</subject><subject>Optic Nerve - metabolism</subject><subject>Phosphatase</subject><subject>Phosphorylation</subject><subject>Population</subject><subject>Predictions</subject><subject>Proteins</subject><subject>Psychiatry</subject><subject>Rodents</subject><subject>Transgenic mice</subject><subject>Transport rate</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1v0zAUhiMEYmPwDxBEQkJw0eKvOM4NUtXxUWli0hjcWifuSesqiYudoPHvcdZsatAucC4c2c95bb_nTZKXlMwpz-mHnet9C_V871qcE8q5EupRckoLzmaSEf746P8keRbCjpCMKymfJicsLioqxWlyfm5DcMZCZ12buipd3Liomn7D3rvK1tBg26VL13bDXHnXpKsupNce2rB3vkuvoMPnyZMK6oAvxvks-fH50_Xy6-zi8stqubiYGVmwbqYIkQXhQGWVE1OqDEqKsqKCUFRFLoziREmec8pKBZDnwEjFMwUCETgKfpa8Pujuaxf0aEDQVBZKUqroQKwOxNrBTu-9bcD_0Q6svl1wfqPBd9bUqCWLjhUoTZYrQZUs1ojlWipmEA0TMmp9HE_rywbXJhrgoZ6ITndau9Ub91uLjAqZD5d5Nwp496vH0OnGBoN1DS26_vbehShYrkhE3_yDPvy6kdpAfIBtKxfPNYOoXgjGijhYFqn5A1T81thYE9MS24rTgveTAjN0-6bbQB-CXn2_-n_28ueUfXvEbhHqbhtc3Q9RC1NQHEDjXQgeq3uTKdFD2O_c0EPY9Rj2WPbquEH3RXfp5n8B4-z33w</recordid><startdate>20150724</startdate><enddate>20150724</enddate><creator>Yuan, Aidong</creator><creator>Hassinger, Linda</creator><creator>Rao, Mala V</creator><creator>Julien, Jean-Pierre</creator><creator>Miller, Christopher C J</creator><creator>Nixon, Ralph A</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150724</creationdate><title>Dissociation of Axonal Neurofilament Content from Its Transport Rate</title><author>Yuan, Aidong ; Hassinger, Linda ; Rao, Mala V ; Julien, Jean-Pierre ; Miller, Christopher C J ; Nixon, Ralph A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-8006903a16f70cb85ab1e6f1401e8974c8308637312b8aa77a20f358a4eea3e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Axonal Transport</topic><topic>Axons</topic><topic>Axons - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yuan, Aidong</au><au>Hassinger, Linda</au><au>Rao, Mala V</au><au>Julien, Jean-Pierre</au><au>Miller, Christopher C J</au><au>Nixon, Ralph A</au><au>Reddy, Hemachandra</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dissociation of Axonal Neurofilament Content from Its Transport Rate</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-07-24</date><risdate>2015</risdate><volume>10</volume><issue>7</issue><spage>e0133848</spage><epage>e0133848</epage><pages>e0133848-e0133848</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>The axonal cytoskeleton of neurofilament (NF) is a long-lived network of fibrous elements believed to be a stationary structure maintained by a small pool of transported cytoskeletal precursors. Accordingly, it may be predicted that NF content in axons can vary independently from the transport rate of NF. In the present report, we confirm this prediction by showing that human NFH transgenic mice and transgenic mice expressing human NFL Ser55 (Asp) develop nearly identical abnormal patterns of NF accumulation and distribution in association with opposite changes in NF slow transport rates. We also show that the rate of NF transport in wild-type mice remains constant along a length of the optic axon where NF content varies 3-fold. Moreover, knockout mice lacking NFH develop even more extreme (6-fold) proximal to distal variation in NF number, which is associated with a normal wild-type rate of NF transport. The independence of regional NF content and NF transport is consistent with previous evidence suggesting that the rate of incorporation of transported NF precursors into a metabolically stable stationary cytoskeletal network is the major determinant of axonal NF content, enabling the generation of the striking local variations in NF number seen along axons.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26208164</pmid><doi>10.1371/journal.pone.0133848</doi><oa>free_for_read</oa></addata></record> |
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subjects | Animals Axonal Transport Axons Axons - metabolism Biology Cytoskeleton Dementia Dissociation Female Genetic engineering Humans Immunoglobulins Intermediate Filaments - metabolism Laboratory animals Male Medicine Mice Mice, Knockout Mice, Transgenic Neurochemistry Neurosciences Optic Nerve - metabolism Phosphatase Phosphorylation Population Predictions Proteins Psychiatry Rodents Transgenic mice Transport rate |
title | Dissociation of Axonal Neurofilament Content from Its Transport Rate |
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