Expression of transcription factors and signaling molecules in the cerebellar granule cell development
Cerebellar granule cell precursors (GCPs) and granule cells (GCs) constitute a good model system to investigate proliferation of neural precursors and differentiation of neurons. During development, GCPs proliferate in the outer external granule cell layer (outer EGL) and then exit the cell cycle in...
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creator | Shiraishi, Ryo D. Miyashita, Sathoshi Yamashita, Mariko Adachi, Toma Shimoda, Mana M. Owa, Tomoo Hoshino, Mikio |
description | Cerebellar granule cell precursors (GCPs) and granule cells (GCs) constitute a good model system to investigate proliferation of neural precursors and differentiation of neurons. During development, GCPs proliferate in the outer external granule cell layer (outer EGL) and then exit the cell cycle in the inner EGL to become GCs, which inwardly migrate to the inner granule cell layer (IGL). Misregulation of GCP proliferation or GC differentiation leads to maldevelopment of the cerebellum and the formation of a cerebellar tumor, medulloblastoma. Despite many efforts in this field, the mechanisms underlying GC development remain elusive. In this study, we performed detailed immunostaining in the developing cerebellum, with particular focus on GCPs and GCs, looking at several transcription factors, signaling molecules, cell cycle regulators, some of which are known to regulate neural development. Interestingly, we found distinct distribution patterns of certain proteins within the outer and inner EGL, suggesting the existence of subpopulations of GCPs and GCs in those layers. This study provides a basis for future studies on the cerebellar GC development and medulloblastoma. |
doi_str_mv | 10.1016/j.gep.2019.119068 |
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During development, GCPs proliferate in the outer external granule cell layer (outer EGL) and then exit the cell cycle in the inner EGL to become GCs, which inwardly migrate to the inner granule cell layer (IGL). Misregulation of GCP proliferation or GC differentiation leads to maldevelopment of the cerebellum and the formation of a cerebellar tumor, medulloblastoma. Despite many efforts in this field, the mechanisms underlying GC development remain elusive. In this study, we performed detailed immunostaining in the developing cerebellum, with particular focus on GCPs and GCs, looking at several transcription factors, signaling molecules, cell cycle regulators, some of which are known to regulate neural development. Interestingly, we found distinct distribution patterns of certain proteins within the outer and inner EGL, suggesting the existence of subpopulations of GCPs and GCs in those layers. This study provides a basis for future studies on the cerebellar GC development and medulloblastoma.</description><identifier>ISSN: 1567-133X</identifier><identifier>EISSN: 1872-7298</identifier><identifier>DOI: 10.1016/j.gep.2019.119068</identifier><identifier>PMID: 31437514</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Basic Helix-Loop-Helix Transcription Factors - metabolism ; Cell Cycle ; Cell cycle regulator ; Cell Differentiation - physiology ; Cell Division ; Cell Proliferation ; Cerebellar granule cell development ; Cerebellum - metabolism ; Immunohistochemistry - methods ; Ki-67 Antigen - metabolism ; Medulloblastoma - metabolism ; Medulloblastoma - physiopathology ; Mice ; Mice, Inbred ICR ; Neurogenesis - physiology ; Neurons - metabolism ; Signal pathway ; Signal Transduction ; Transcription Factors - metabolism ; Transcriptional factor</subject><ispartof>Gene Expression Patterns, 2019-12, Vol.34, p.119068-119068, Article 119068</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c503t-f752bd93aa6d1c0fc872fd00fbae06ecae222672c75b2a03c32b7172a60f66b33</citedby><cites>FETCH-LOGICAL-c503t-f752bd93aa6d1c0fc872fd00fbae06ecae222672c75b2a03c32b7172a60f66b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1567133X19300596$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31437514$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shiraishi, Ryo D.</creatorcontrib><creatorcontrib>Miyashita, Sathoshi</creatorcontrib><creatorcontrib>Yamashita, Mariko</creatorcontrib><creatorcontrib>Adachi, Toma</creatorcontrib><creatorcontrib>Shimoda, Mana M.</creatorcontrib><creatorcontrib>Owa, Tomoo</creatorcontrib><creatorcontrib>Hoshino, Mikio</creatorcontrib><title>Expression of transcription factors and signaling molecules in the cerebellar granule cell development</title><title>Gene Expression Patterns</title><addtitle>Gene Expr Patterns</addtitle><description>Cerebellar granule cell precursors (GCPs) and granule cells (GCs) constitute a good model system to investigate proliferation of neural precursors and differentiation of neurons. 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This study provides a basis for future studies on the cerebellar GC development and medulloblastoma.</description><subject>Animals</subject><subject>Basic Helix-Loop-Helix Transcription Factors - metabolism</subject><subject>Cell Cycle</subject><subject>Cell cycle regulator</subject><subject>Cell Differentiation - physiology</subject><subject>Cell Division</subject><subject>Cell Proliferation</subject><subject>Cerebellar granule cell development</subject><subject>Cerebellum - metabolism</subject><subject>Immunohistochemistry - methods</subject><subject>Ki-67 Antigen - metabolism</subject><subject>Medulloblastoma - metabolism</subject><subject>Medulloblastoma - physiopathology</subject><subject>Mice</subject><subject>Mice, Inbred ICR</subject><subject>Neurogenesis - physiology</subject><subject>Neurons - metabolism</subject><subject>Signal pathway</subject><subject>Signal Transduction</subject><subject>Transcription Factors - metabolism</subject><subject>Transcriptional factor</subject><issn>1567-133X</issn><issn>1872-7298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1rGzEQhkVpaBy3P6CXomMu6-hjV9qlpxKcDzDkkkBuQqsduTJaaSutTfLvI-Mkx55mmHnfl5kHoZ-UrCih4mq32sK0YoR2K0o7ItovaEFbySrJuvZr6RshK8r58zm6yHlHiqcT3Td0zmnNZUPrBbLrlylBzi4GHC2ekw7ZJDfNx4HVZo4pYx0GnN02aO_CFo_Rg9l7yNgFPP8FbCBBD97rhLfFX1Zl5D0e4AA-TiOE-Ts6s9pn-PFel-jpZv14fVdtHm7vr_9sKtMQPldWNqwfOq61GKgh1pRn7ECI7TUQAUYDY0xIZmTTM0244ayXVDItiBWi53yJLk-5U4r_9pBnNbp8PEYHiPusGGtpWze1rIuUnqQmxZwTWDUlN-r0qihRR7xqpwpedcSrTniL59d7_L4fYfh0fPAsgt8nAZQnDw6SysZBMDC4BGZWQ3T_iX8DhLyNCA</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Shiraishi, Ryo D.</creator><creator>Miyashita, Sathoshi</creator><creator>Yamashita, Mariko</creator><creator>Adachi, Toma</creator><creator>Shimoda, Mana M.</creator><creator>Owa, Tomoo</creator><creator>Hoshino, Mikio</creator><general>Elsevier B.V</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></search><sort><creationdate>20191201</creationdate><title>Expression of transcription factors and signaling molecules in the cerebellar granule cell development</title><author>Shiraishi, Ryo D. ; Miyashita, Sathoshi ; Yamashita, Mariko ; Adachi, Toma ; Shimoda, Mana M. ; Owa, Tomoo ; Hoshino, Mikio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c503t-f752bd93aa6d1c0fc872fd00fbae06ecae222672c75b2a03c32b7172a60f66b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Basic Helix-Loop-Helix Transcription Factors - metabolism</topic><topic>Cell Cycle</topic><topic>Cell cycle regulator</topic><topic>Cell Differentiation - physiology</topic><topic>Cell Division</topic><topic>Cell Proliferation</topic><topic>Cerebellar granule cell development</topic><topic>Cerebellum - metabolism</topic><topic>Immunohistochemistry - methods</topic><topic>Ki-67 Antigen - metabolism</topic><topic>Medulloblastoma - metabolism</topic><topic>Medulloblastoma - physiopathology</topic><topic>Mice</topic><topic>Mice, Inbred ICR</topic><topic>Neurogenesis - physiology</topic><topic>Neurons - metabolism</topic><topic>Signal pathway</topic><topic>Signal Transduction</topic><topic>Transcription Factors - metabolism</topic><topic>Transcriptional factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shiraishi, Ryo D.</creatorcontrib><creatorcontrib>Miyashita, Sathoshi</creatorcontrib><creatorcontrib>Yamashita, Mariko</creatorcontrib><creatorcontrib>Adachi, Toma</creatorcontrib><creatorcontrib>Shimoda, Mana M.</creatorcontrib><creatorcontrib>Owa, Tomoo</creatorcontrib><creatorcontrib>Hoshino, Mikio</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><jtitle>Gene Expression Patterns</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shiraishi, Ryo D.</au><au>Miyashita, Sathoshi</au><au>Yamashita, Mariko</au><au>Adachi, Toma</au><au>Shimoda, Mana M.</au><au>Owa, Tomoo</au><au>Hoshino, Mikio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of transcription factors and signaling molecules in the cerebellar granule cell development</atitle><jtitle>Gene Expression Patterns</jtitle><addtitle>Gene Expr Patterns</addtitle><date>2019-12-01</date><risdate>2019</risdate><volume>34</volume><spage>119068</spage><epage>119068</epage><pages>119068-119068</pages><artnum>119068</artnum><issn>1567-133X</issn><eissn>1872-7298</eissn><abstract>Cerebellar granule cell precursors (GCPs) and granule cells (GCs) constitute a good model system to investigate proliferation of neural precursors and differentiation of neurons. During development, GCPs proliferate in the outer external granule cell layer (outer EGL) and then exit the cell cycle in the inner EGL to become GCs, which inwardly migrate to the inner granule cell layer (IGL). Misregulation of GCP proliferation or GC differentiation leads to maldevelopment of the cerebellum and the formation of a cerebellar tumor, medulloblastoma. Despite many efforts in this field, the mechanisms underlying GC development remain elusive. In this study, we performed detailed immunostaining in the developing cerebellum, with particular focus on GCPs and GCs, looking at several transcription factors, signaling molecules, cell cycle regulators, some of which are known to regulate neural development. Interestingly, we found distinct distribution patterns of certain proteins within the outer and inner EGL, suggesting the existence of subpopulations of GCPs and GCs in those layers. 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subjects | Animals Basic Helix-Loop-Helix Transcription Factors - metabolism Cell Cycle Cell cycle regulator Cell Differentiation - physiology Cell Division Cell Proliferation Cerebellar granule cell development Cerebellum - metabolism Immunohistochemistry - methods Ki-67 Antigen - metabolism Medulloblastoma - metabolism Medulloblastoma - physiopathology Mice Mice, Inbred ICR Neurogenesis - physiology Neurons - metabolism Signal pathway Signal Transduction Transcription Factors - metabolism Transcriptional factor |
title | Expression of transcription factors and signaling molecules in the cerebellar granule cell development |
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