Loading…
Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus
Accumulation of the heavy‐chain neurofilaments reflects the maturation status of neuronal structures. The spatial distribution and postnatal developmental dynamic of neurons expressing nonphosphorylated heavy‐chain neurofilaments (labeled by SMI‐32 antibody) were analyzed in the dorsal lateral genic...
Saved in:
Published in: | Journal of comparative neurology (1911) 2021-05, Vol.529 (7), p.1430-1441 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3 |
---|---|
cites | cdi_FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3 |
container_end_page | 1441 |
container_issue | 7 |
container_start_page | 1430 |
container_title | Journal of comparative neurology (1911) |
container_volume | 529 |
creator | Mikhalkin, Aleksandr Nikitina, Nina Merkulyeva, Natalia |
description | Accumulation of the heavy‐chain neurofilaments reflects the maturation status of neuronal structures. The spatial distribution and postnatal developmental dynamic of neurons expressing nonphosphorylated heavy‐chain neurofilaments (labeled by SMI‐32 antibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat. Both interlaminar and intralaminar differences in the dynamic of SMI‐32 staining were observed. The following results were obtained: (a) Ascending dorsoventral gradient in the density of SMI‐32 immunopositive (SMI‐32(+)) neurons (the greatest neuronal density in layer Cm, the minor in the top sublayer of layer A). This gradient was most prominent at the earliest stages of postnatal development (1st–2nd weeks) and slowly flattened up to adulthood; (b) Layer A1 exhibits increases in SMI‐32‐positive cells earlier than layer A; (c) The general transient increment in the number and density of SMI‐32(+) neurons around 2–5 postnatal weeks. Since SMI‐32 antibody is considered to be a putative marker for Y cells forming a motion processing stream, we suggest that peculiarities of SMI‐32 staining at geniculate level could reflect the heterogeneity of Y cell subpopulations and the heterochrony of their postnatal maturation.
Postnatal development of the SMI‐32 labeling in the dorsal lateral geniculate nucleus (LGNd) of kittens aged 0–123 postnatal days, and in adults (Ad). Left—a representational examples of the SMI‐32 labeling, in kittens aged 0 days, 10 days, and in adult. Right—a number of SMI‐32 immunopositive (SMI‐32(+)) neurons in layers A, A1, and Cm of the LGNd. Different phases of the postnatal development (eyes opening, precritical period, critical period maximum) are marked by colors. |
doi_str_mv | 10.1002/cne.25028 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2441260150</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2509242322</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3</originalsourceid><addsrcrecordid>eNp1kc9O3DAQxi1UxG6BAy9QWeJCDwH_WSfxEa1oQULl0p4tx5mQrBJ7a8etcuMNyjPyJHUa6KFSD9bIM7_5xuMPoTNKLikh7MpYuGSCsPIArSmReSbLnL5D61SjmZR5sULvQ9gRQqTk5RFacSYJlWyzRr9uYQTvTOudnbBr8N6F0epR91gbE4fY67Fzdq5YZ_etC-n4KWWhxi3oH9PL07NpdWexhehd0_V6ADvialoSNsy9YwvY6BHXzockPbf7FB_BdmYeAdhG00MMJ-iw0X2A09d4jL59uvm6vc3uHz7fba_vM8MFLzNpGmoqJmRdFUU978WatI-uOM-rqq7KgtZUlJRrmYuUz4UgErQhDU1Xavgxulh09959jxBGNXTBQN9rCy4GxTYbynJCBUno-T_ozkVv0-tU-vQ0lXHGEvVxoYx3IXho1N53g_aTokTNLqnkkvrjUmI_vCrGaoD6L_lmSwKuFuBn18P0fyW1_XKzSP4Gh42fOA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2509242322</pqid></control><display><type>article</type><title>Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Mikhalkin, Aleksandr ; Nikitina, Nina ; Merkulyeva, Natalia</creator><creatorcontrib>Mikhalkin, Aleksandr ; Nikitina, Nina ; Merkulyeva, Natalia</creatorcontrib><description>Accumulation of the heavy‐chain neurofilaments reflects the maturation status of neuronal structures. The spatial distribution and postnatal developmental dynamic of neurons expressing nonphosphorylated heavy‐chain neurofilaments (labeled by SMI‐32 antibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat. Both interlaminar and intralaminar differences in the dynamic of SMI‐32 staining were observed. The following results were obtained: (a) Ascending dorsoventral gradient in the density of SMI‐32 immunopositive (SMI‐32(+)) neurons (the greatest neuronal density in layer Cm, the minor in the top sublayer of layer A). This gradient was most prominent at the earliest stages of postnatal development (1st–2nd weeks) and slowly flattened up to adulthood; (b) Layer A1 exhibits increases in SMI‐32‐positive cells earlier than layer A; (c) The general transient increment in the number and density of SMI‐32(+) neurons around 2–5 postnatal weeks. Since SMI‐32 antibody is considered to be a putative marker for Y cells forming a motion processing stream, we suggest that peculiarities of SMI‐32 staining at geniculate level could reflect the heterogeneity of Y cell subpopulations and the heterochrony of their postnatal maturation.
Postnatal development of the SMI‐32 labeling in the dorsal lateral geniculate nucleus (LGNd) of kittens aged 0–123 postnatal days, and in adults (Ad). Left—a representational examples of the SMI‐32 labeling, in kittens aged 0 days, 10 days, and in adult. Right—a number of SMI‐32 immunopositive (SMI‐32(+)) neurons in layers A, A1, and Cm of the LGNd. Different phases of the postnatal development (eyes opening, precritical period, critical period maximum) are marked by colors.</description><identifier>ISSN: 0021-9967</identifier><identifier>EISSN: 1096-9861</identifier><identifier>DOI: 10.1002/cne.25028</identifier><identifier>PMID: 32901924</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Animals ; cat ; Cats ; critical period ; Developmental stages ; Female ; Geniculate Bodies - cytology ; interlaminar differences ; Lateral geniculate nucleus ; Male ; Motion detection ; Neurofilament Proteins - analysis ; Neurofilaments ; Neurogenesis - physiology ; Neurons ; Neurons - cytology ; postnatal development ; RRID: AB_2715852 ; Spatial distribution ; Y cells</subject><ispartof>Journal of comparative neurology (1911), 2021-05, Vol.529 (7), p.1430-1441</ispartof><rights>2020 Wiley Periodicals LLC</rights><rights>2020 Wiley Periodicals LLC.</rights><rights>2021 Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3</citedby><cites>FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3</cites><orcidid>0000-0003-2342-6357 ; 0000-0003-1276-1918</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32901924$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mikhalkin, Aleksandr</creatorcontrib><creatorcontrib>Nikitina, Nina</creatorcontrib><creatorcontrib>Merkulyeva, Natalia</creatorcontrib><title>Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus</title><title>Journal of comparative neurology (1911)</title><addtitle>J Comp Neurol</addtitle><description>Accumulation of the heavy‐chain neurofilaments reflects the maturation status of neuronal structures. The spatial distribution and postnatal developmental dynamic of neurons expressing nonphosphorylated heavy‐chain neurofilaments (labeled by SMI‐32 antibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat. Both interlaminar and intralaminar differences in the dynamic of SMI‐32 staining were observed. The following results were obtained: (a) Ascending dorsoventral gradient in the density of SMI‐32 immunopositive (SMI‐32(+)) neurons (the greatest neuronal density in layer Cm, the minor in the top sublayer of layer A). This gradient was most prominent at the earliest stages of postnatal development (1st–2nd weeks) and slowly flattened up to adulthood; (b) Layer A1 exhibits increases in SMI‐32‐positive cells earlier than layer A; (c) The general transient increment in the number and density of SMI‐32(+) neurons around 2–5 postnatal weeks. Since SMI‐32 antibody is considered to be a putative marker for Y cells forming a motion processing stream, we suggest that peculiarities of SMI‐32 staining at geniculate level could reflect the heterogeneity of Y cell subpopulations and the heterochrony of their postnatal maturation.
Postnatal development of the SMI‐32 labeling in the dorsal lateral geniculate nucleus (LGNd) of kittens aged 0–123 postnatal days, and in adults (Ad). Left—a representational examples of the SMI‐32 labeling, in kittens aged 0 days, 10 days, and in adult. Right—a number of SMI‐32 immunopositive (SMI‐32(+)) neurons in layers A, A1, and Cm of the LGNd. Different phases of the postnatal development (eyes opening, precritical period, critical period maximum) are marked by colors.</description><subject>Animals</subject><subject>cat</subject><subject>Cats</subject><subject>critical period</subject><subject>Developmental stages</subject><subject>Female</subject><subject>Geniculate Bodies - cytology</subject><subject>interlaminar differences</subject><subject>Lateral geniculate nucleus</subject><subject>Male</subject><subject>Motion detection</subject><subject>Neurofilament Proteins - analysis</subject><subject>Neurofilaments</subject><subject>Neurogenesis - physiology</subject><subject>Neurons</subject><subject>Neurons - cytology</subject><subject>postnatal development</subject><subject>RRID: AB_2715852</subject><subject>Spatial distribution</subject><subject>Y cells</subject><issn>0021-9967</issn><issn>1096-9861</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kc9O3DAQxi1UxG6BAy9QWeJCDwH_WSfxEa1oQULl0p4tx5mQrBJ7a8etcuMNyjPyJHUa6KFSD9bIM7_5xuMPoTNKLikh7MpYuGSCsPIArSmReSbLnL5D61SjmZR5sULvQ9gRQqTk5RFacSYJlWyzRr9uYQTvTOudnbBr8N6F0epR91gbE4fY67Fzdq5YZ_etC-n4KWWhxi3oH9PL07NpdWexhehd0_V6ADvialoSNsy9YwvY6BHXzockPbf7FB_BdmYeAdhG00MMJ-iw0X2A09d4jL59uvm6vc3uHz7fba_vM8MFLzNpGmoqJmRdFUU978WatI-uOM-rqq7KgtZUlJRrmYuUz4UgErQhDU1Xavgxulh09959jxBGNXTBQN9rCy4GxTYbynJCBUno-T_ozkVv0-tU-vQ0lXHGEvVxoYx3IXho1N53g_aTokTNLqnkkvrjUmI_vCrGaoD6L_lmSwKuFuBn18P0fyW1_XKzSP4Gh42fOA</recordid><startdate>20210501</startdate><enddate>20210501</enddate><creator>Mikhalkin, Aleksandr</creator><creator>Nikitina, Nina</creator><creator>Merkulyeva, Natalia</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, 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>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2342-6357</orcidid><orcidid>https://orcid.org/0000-0003-1276-1918</orcidid></search><sort><creationdate>20210501</creationdate><title>Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus</title><author>Mikhalkin, Aleksandr ; Nikitina, Nina ; Merkulyeva, Natalia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>cat</topic><topic>Cats</topic><topic>critical period</topic><topic>Developmental stages</topic><topic>Female</topic><topic>Geniculate Bodies - cytology</topic><topic>interlaminar differences</topic><topic>Lateral geniculate nucleus</topic><topic>Male</topic><topic>Motion detection</topic><topic>Neurofilament Proteins - analysis</topic><topic>Neurofilaments</topic><topic>Neurogenesis - physiology</topic><topic>Neurons</topic><topic>Neurons - cytology</topic><topic>postnatal development</topic><topic>RRID: AB_2715852</topic><topic>Spatial distribution</topic><topic>Y cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mikhalkin, Aleksandr</creatorcontrib><creatorcontrib>Nikitina, Nina</creatorcontrib><creatorcontrib>Merkulyeva, Natalia</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of comparative neurology (1911)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mikhalkin, Aleksandr</au><au>Nikitina, Nina</au><au>Merkulyeva, Natalia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus</atitle><jtitle>Journal of comparative neurology (1911)</jtitle><addtitle>J Comp Neurol</addtitle><date>2021-05-01</date><risdate>2021</risdate><volume>529</volume><issue>7</issue><spage>1430</spage><epage>1441</epage><pages>1430-1441</pages><issn>0021-9967</issn><eissn>1096-9861</eissn><abstract>Accumulation of the heavy‐chain neurofilaments reflects the maturation status of neuronal structures. The spatial distribution and postnatal developmental dynamic of neurons expressing nonphosphorylated heavy‐chain neurofilaments (labeled by SMI‐32 antibody) were analyzed in the dorsal lateral geniculate nucleus (LGNd) of the cat. Both interlaminar and intralaminar differences in the dynamic of SMI‐32 staining were observed. The following results were obtained: (a) Ascending dorsoventral gradient in the density of SMI‐32 immunopositive (SMI‐32(+)) neurons (the greatest neuronal density in layer Cm, the minor in the top sublayer of layer A). This gradient was most prominent at the earliest stages of postnatal development (1st–2nd weeks) and slowly flattened up to adulthood; (b) Layer A1 exhibits increases in SMI‐32‐positive cells earlier than layer A; (c) The general transient increment in the number and density of SMI‐32(+) neurons around 2–5 postnatal weeks. Since SMI‐32 antibody is considered to be a putative marker for Y cells forming a motion processing stream, we suggest that peculiarities of SMI‐32 staining at geniculate level could reflect the heterogeneity of Y cell subpopulations and the heterochrony of their postnatal maturation.
Postnatal development of the SMI‐32 labeling in the dorsal lateral geniculate nucleus (LGNd) of kittens aged 0–123 postnatal days, and in adults (Ad). Left—a representational examples of the SMI‐32 labeling, in kittens aged 0 days, 10 days, and in adult. Right—a number of SMI‐32 immunopositive (SMI‐32(+)) neurons in layers A, A1, and Cm of the LGNd. Different phases of the postnatal development (eyes opening, precritical period, critical period maximum) are marked by colors.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>32901924</pmid><doi>10.1002/cne.25028</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-2342-6357</orcidid><orcidid>https://orcid.org/0000-0003-1276-1918</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-9967 |
ispartof | Journal of comparative neurology (1911), 2021-05, Vol.529 (7), p.1430-1441 |
issn | 0021-9967 1096-9861 |
language | eng |
recordid | cdi_proquest_miscellaneous_2441260150 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Animals cat Cats critical period Developmental stages Female Geniculate Bodies - cytology interlaminar differences Lateral geniculate nucleus Male Motion detection Neurofilament Proteins - analysis Neurofilaments Neurogenesis - physiology Neurons Neurons - cytology postnatal development RRID: AB_2715852 Spatial distribution Y cells |
title | Heterochrony of postnatal accumulation of nonphosphorylated heavy‐chain neurofilament by neurons of the cat dorsal lateral geniculate nucleus |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T10%3A37%3A09IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Heterochrony%20of%20postnatal%20accumulation%20of%20nonphosphorylated%20heavy%E2%80%90chain%20neurofilament%20by%20neurons%20of%20the%20cat%20dorsal%20lateral%20geniculate%20nucleus&rft.jtitle=Journal%20of%20comparative%20neurology%20(1911)&rft.au=Mikhalkin,%20Aleksandr&rft.date=2021-05-01&rft.volume=529&rft.issue=7&rft.spage=1430&rft.epage=1441&rft.pages=1430-1441&rft.issn=0021-9967&rft.eissn=1096-9861&rft_id=info:doi/10.1002/cne.25028&rft_dat=%3Cproquest_cross%3E2509242322%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3538-9cf1cb259db77d00992f924ab336bbdb871d15813a96524a65509eac0f15241c3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2509242322&rft_id=info:pmid/32901924&rfr_iscdi=true |