Branch management: mechanisms of axon branching in the developing vertebrate CNS
Key Points Axon branching connects single neurons with multiple targets, which, along with the formation of highly branched terminal arbors, underlies the complex circuitry of the vertebrate CNS. Axon collateral branches extend interstitially from the axon shaft as dynamic filopodia that develop int...
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description | Key Points
Axon branching connects single neurons with multiple targets, which, along with the formation of highly branched terminal arbors, underlies the complex circuitry of the vertebrate CNS.
Axon collateral branches extend interstitially from the axon shaft as dynamic filopodia that develop into branches at appropriate targets regions to form functional maps. Extrinsic guidance cues, growth factors and morphogens regulate axon branching and shape terminal arbors that develop from axon branches.
Growth and guidance of axon branches in response to extracellular cues require dynamic reorganization of the actin and microtubule cytoskeleton. Cycles of cytoskeletal polymerization and depolymerization are highly regulated by actin- and microtubule-associated proteins during branch formation.
Complex signalling pathways that are activated by extracellular cues through their receptors regulate axon branching. The ultimate target of signal transduction pathways is the cytoskeleton, which can reorganize by changes in dynamics to promote or suppress axon branching.
Neuronal activity, which is often stimulated by extracellular cues, can regulate axon branching by transient fluctuations in the levels of intracellular calcium, which acts as a second messenger to activate downstream cytoskeletal effectors. Effects of neural activity can involve competition among neighbouring axon arbors, such as in the retinotectal system, where competitive activity-dependent mechanisms regulate arbor size and complexity.
Future directions in the study of axon branch formation will involve the use of preparations of the vertebrate CNS that recapitulate the complexity of the
in vivo
environment. Improvements in labelling techniques and high-resolution time-lapse microscopy should facilitate such studies.
To enable the complex neural circuitry found in vertebrates, many axons undergo extensive branching. Here, Kalil and Dent review the roles of extracellular cues, intracellular signalling pathways, cytoskeletal dynamics and neuronal activity in axon branching and terminal arbor formation in the vertebrate CNS.
The remarkable ability of a single axon to extend multiple branches and form terminal arbors enables vertebrate neurons to integrate information from divergent regions of the nervous system. Axons select appropriate pathways during development, but it is the branches that extend interstitially from the axon shaft and arborize at specific targets that are responsible for virtually |
doi_str_mv | 10.1038/nrn3650 |
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Axon branching connects single neurons with multiple targets, which, along with the formation of highly branched terminal arbors, underlies the complex circuitry of the vertebrate CNS.
Axon collateral branches extend interstitially from the axon shaft as dynamic filopodia that develop into branches at appropriate targets regions to form functional maps. Extrinsic guidance cues, growth factors and morphogens regulate axon branching and shape terminal arbors that develop from axon branches.
Growth and guidance of axon branches in response to extracellular cues require dynamic reorganization of the actin and microtubule cytoskeleton. Cycles of cytoskeletal polymerization and depolymerization are highly regulated by actin- and microtubule-associated proteins during branch formation.
Complex signalling pathways that are activated by extracellular cues through their receptors regulate axon branching. The ultimate target of signal transduction pathways is the cytoskeleton, which can reorganize by changes in dynamics to promote or suppress axon branching.
Neuronal activity, which is often stimulated by extracellular cues, can regulate axon branching by transient fluctuations in the levels of intracellular calcium, which acts as a second messenger to activate downstream cytoskeletal effectors. Effects of neural activity can involve competition among neighbouring axon arbors, such as in the retinotectal system, where competitive activity-dependent mechanisms regulate arbor size and complexity.
Future directions in the study of axon branch formation will involve the use of preparations of the vertebrate CNS that recapitulate the complexity of the
in vivo
environment. Improvements in labelling techniques and high-resolution time-lapse microscopy should facilitate such studies.
To enable the complex neural circuitry found in vertebrates, many axons undergo extensive branching. Here, Kalil and Dent review the roles of extracellular cues, intracellular signalling pathways, cytoskeletal dynamics and neuronal activity in axon branching and terminal arbor formation in the vertebrate CNS.
The remarkable ability of a single axon to extend multiple branches and form terminal arbors enables vertebrate neurons to integrate information from divergent regions of the nervous system. Axons select appropriate pathways during development, but it is the branches that extend interstitially from the axon shaft and arborize at specific targets that are responsible for virtually all of the synaptic connectivity in the vertebrate CNS. How do axons form branches at specific target regions? Recent studies have identified molecular cues that activate intracellular signalling pathways in axons and mediate dynamic reorganization of the cytoskeleton to promote the formation of axon branches.</description><identifier>ISSN: 1471-003X</identifier><identifier>EISSN: 1471-0048</identifier><identifier>EISSN: 1469-3178</identifier><identifier>DOI: 10.1038/nrn3650</identifier><identifier>PMID: 24356070</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>14 ; 14/69 ; 631/378/2571 ; 631/378/2571/2576 ; 631/80/128/1276 ; 631/80/128/1653 ; Animal Genetics and Genomics ; Animals ; Axons ; Axons - physiology ; Behavioral Sciences ; Biological Techniques ; Biomedicine ; Brain - embryology ; Brain - growth & development ; Genetic aspects ; Humans ; Nervous system ; Neurobiology ; Neurogenesis ; Neurogenesis - physiology ; Neurosciences ; Physiological aspects ; Retina ; review-article ; Topography ; Vertebrates</subject><ispartof>Nature reviews. Neuroscience, 2014-01, Vol.15 (1), p.7-18</ispartof><rights>Springer Nature Limited 2014</rights><rights>COPYRIGHT 2014 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jan 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c596t-1b00a916c7e9d2fa9138d8436a2542603f73feb83e7dbf68ddb3ae6cdc4a35723</citedby><cites>FETCH-LOGICAL-c596t-1b00a916c7e9d2fa9138d8436a2542603f73feb83e7dbf68ddb3ae6cdc4a35723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nrn3650$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nrn3650$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,777,781,882,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24356070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kalil, Katherine</creatorcontrib><creatorcontrib>Dent, Erik W.</creatorcontrib><title>Branch management: mechanisms of axon branching in the developing vertebrate CNS</title><title>Nature reviews. Neuroscience</title><addtitle>Nat Rev Neurosci</addtitle><addtitle>Nat Rev Neurosci</addtitle><description>Key Points
Axon branching connects single neurons with multiple targets, which, along with the formation of highly branched terminal arbors, underlies the complex circuitry of the vertebrate CNS.
Axon collateral branches extend interstitially from the axon shaft as dynamic filopodia that develop into branches at appropriate targets regions to form functional maps. Extrinsic guidance cues, growth factors and morphogens regulate axon branching and shape terminal arbors that develop from axon branches.
Growth and guidance of axon branches in response to extracellular cues require dynamic reorganization of the actin and microtubule cytoskeleton. Cycles of cytoskeletal polymerization and depolymerization are highly regulated by actin- and microtubule-associated proteins during branch formation.
Complex signalling pathways that are activated by extracellular cues through their receptors regulate axon branching. The ultimate target of signal transduction pathways is the cytoskeleton, which can reorganize by changes in dynamics to promote or suppress axon branching.
Neuronal activity, which is often stimulated by extracellular cues, can regulate axon branching by transient fluctuations in the levels of intracellular calcium, which acts as a second messenger to activate downstream cytoskeletal effectors. Effects of neural activity can involve competition among neighbouring axon arbors, such as in the retinotectal system, where competitive activity-dependent mechanisms regulate arbor size and complexity.
Future directions in the study of axon branch formation will involve the use of preparations of the vertebrate CNS that recapitulate the complexity of the
in vivo
environment. Improvements in labelling techniques and high-resolution time-lapse microscopy should facilitate such studies.
To enable the complex neural circuitry found in vertebrates, many axons undergo extensive branching. Here, Kalil and Dent review the roles of extracellular cues, intracellular signalling pathways, cytoskeletal dynamics and neuronal activity in axon branching and terminal arbor formation in the vertebrate CNS.
The remarkable ability of a single axon to extend multiple branches and form terminal arbors enables vertebrate neurons to integrate information from divergent regions of the nervous system. Axons select appropriate pathways during development, but it is the branches that extend interstitially from the axon shaft and arborize at specific targets that are responsible for virtually all of the synaptic connectivity in the vertebrate CNS. How do axons form branches at specific target regions? Recent studies have identified molecular cues that activate intracellular signalling pathways in axons and mediate dynamic reorganization of the cytoskeleton to promote the formation of axon branches.</description><subject>14</subject><subject>14/69</subject><subject>631/378/2571</subject><subject>631/378/2571/2576</subject><subject>631/80/128/1276</subject><subject>631/80/128/1653</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Axons</subject><subject>Axons - physiology</subject><subject>Behavioral Sciences</subject><subject>Biological Techniques</subject><subject>Biomedicine</subject><subject>Brain - embryology</subject><subject>Brain - growth & development</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Nervous system</subject><subject>Neurobiology</subject><subject>Neurogenesis</subject><subject>Neurogenesis - physiology</subject><subject>Neurosciences</subject><subject>Physiological aspects</subject><subject>Retina</subject><subject>review-article</subject><subject>Topography</subject><subject>Vertebrates</subject><issn>1471-003X</issn><issn>1471-0048</issn><issn>1469-3178</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</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><recordid>eNqFkkuLFDEQxxtR3HUVv4EEPOhl1qTz6ngQ1sEXLCqo4C2kk0pPlu5kTHoG_fZm3HH2gSA5VFH1qz9VlWqaxwSfEky7FzFHKji-0xwTJskCY9bdPfj0-1HzoJQLjIkgUtxvjlpGucASHzefX2cT7QpNJpoBJojzSzSBXZkYylRQ8sj8TBH1f6gQBxQimleAHGxhTOtdZAt5hgrMgJYfvzxs7nkzFni0tyfNt7dvvi7fL84_vfuwPDtfWK7EvCA9xkYRYSUo1_rq0s51jArTctYKTL2kHvqOgnS9F51zPTUgrLPMUC5betK8utRdb_oJnK2dZzPqdQ6Tyb90MkHfzMSw0kPaaoYFbRWuAs_3Ajn92ECZ9RSKhXE0EdKmaMI5U0wp1f4fZQrL2pWgFX16C71ImxzrJjQRAgvRSSGuqMGMoEP0qbZod6L6rP4M71rCd1qn_6DqczAFmyL4UOM3Cp5dFticSsngD-sgWO_uRO_vpJJPrm_vwP09jKuRS03FAfK1OW5p_QY-H8RV</recordid><startdate>20140101</startdate><enddate>20140101</enddate><creator>Kalil, Katherine</creator><creator>Dent, Erik W.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</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>3V.</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140101</creationdate><title>Branch management: mechanisms of axon branching in the developing vertebrate CNS</title><author>Kalil, Katherine ; Dent, Erik W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c596t-1b00a916c7e9d2fa9138d8436a2542603f73feb83e7dbf68ddb3ae6cdc4a35723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>14</topic><topic>14/69</topic><topic>631/378/2571</topic><topic>631/378/2571/2576</topic><topic>631/80/128/1276</topic><topic>631/80/128/1653</topic><topic>Animal Genetics and Genomics</topic><topic>Animals</topic><topic>Axons</topic><topic>Axons - physiology</topic><topic>Behavioral Sciences</topic><topic>Biological Techniques</topic><topic>Biomedicine</topic><topic>Brain - embryology</topic><topic>Brain - growth & development</topic><topic>Genetic aspects</topic><topic>Humans</topic><topic>Nervous system</topic><topic>Neurobiology</topic><topic>Neurogenesis</topic><topic>Neurogenesis - physiology</topic><topic>Neurosciences</topic><topic>Physiological aspects</topic><topic>Retina</topic><topic>review-article</topic><topic>Topography</topic><topic>Vertebrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kalil, Katherine</creatorcontrib><creatorcontrib>Dent, Erik W.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Psychology Journals</collection><collection>ProQuest Biological Science Journals</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Nature reviews. Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kalil, Katherine</au><au>Dent, Erik W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Branch management: mechanisms of axon branching in the developing vertebrate CNS</atitle><jtitle>Nature reviews. Neuroscience</jtitle><stitle>Nat Rev Neurosci</stitle><addtitle>Nat Rev Neurosci</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>15</volume><issue>1</issue><spage>7</spage><epage>18</epage><pages>7-18</pages><issn>1471-003X</issn><eissn>1471-0048</eissn><eissn>1469-3178</eissn><abstract>Key Points
Axon branching connects single neurons with multiple targets, which, along with the formation of highly branched terminal arbors, underlies the complex circuitry of the vertebrate CNS.
Axon collateral branches extend interstitially from the axon shaft as dynamic filopodia that develop into branches at appropriate targets regions to form functional maps. Extrinsic guidance cues, growth factors and morphogens regulate axon branching and shape terminal arbors that develop from axon branches.
Growth and guidance of axon branches in response to extracellular cues require dynamic reorganization of the actin and microtubule cytoskeleton. Cycles of cytoskeletal polymerization and depolymerization are highly regulated by actin- and microtubule-associated proteins during branch formation.
Complex signalling pathways that are activated by extracellular cues through their receptors regulate axon branching. The ultimate target of signal transduction pathways is the cytoskeleton, which can reorganize by changes in dynamics to promote or suppress axon branching.
Neuronal activity, which is often stimulated by extracellular cues, can regulate axon branching by transient fluctuations in the levels of intracellular calcium, which acts as a second messenger to activate downstream cytoskeletal effectors. Effects of neural activity can involve competition among neighbouring axon arbors, such as in the retinotectal system, where competitive activity-dependent mechanisms regulate arbor size and complexity.
Future directions in the study of axon branch formation will involve the use of preparations of the vertebrate CNS that recapitulate the complexity of the
in vivo
environment. Improvements in labelling techniques and high-resolution time-lapse microscopy should facilitate such studies.
To enable the complex neural circuitry found in vertebrates, many axons undergo extensive branching. Here, Kalil and Dent review the roles of extracellular cues, intracellular signalling pathways, cytoskeletal dynamics and neuronal activity in axon branching and terminal arbor formation in the vertebrate CNS.
The remarkable ability of a single axon to extend multiple branches and form terminal arbors enables vertebrate neurons to integrate information from divergent regions of the nervous system. Axons select appropriate pathways during development, but it is the branches that extend interstitially from the axon shaft and arborize at specific targets that are responsible for virtually all of the synaptic connectivity in the vertebrate CNS. How do axons form branches at specific target regions? Recent studies have identified molecular cues that activate intracellular signalling pathways in axons and mediate dynamic reorganization of the cytoskeleton to promote the formation of axon branches.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>24356070</pmid><doi>10.1038/nrn3650</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 14 14/69 631/378/2571 631/378/2571/2576 631/80/128/1276 631/80/128/1653 Animal Genetics and Genomics Animals Axons Axons - physiology Behavioral Sciences Biological Techniques Biomedicine Brain - embryology Brain - growth & development Genetic aspects Humans Nervous system Neurobiology Neurogenesis Neurogenesis - physiology Neurosciences Physiological aspects Retina review-article Topography Vertebrates |
title | Branch management: mechanisms of axon branching in the developing vertebrate CNS |
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