Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김두리 | - |
dc.date.accessioned | 2022-08-08T01:58:08Z | - |
dc.date.available | 2022-08-08T01:58:08Z | - |
dc.date.issued | 2020-11 | - |
dc.identifier.citation | FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, v. 8, article no. 588556, page. 1-17 | en_US |
dc.identifier.issn | 2296-634X | - |
dc.identifier.uri | https://www.frontiersin.org/articles/10.3389/fcell.2020.588556/full | - |
dc.identifier.uri | https://repository.hanyang.ac.kr/handle/20.500.11754/172206 | - |
dc.description.abstract | Actin networks and actin-binding proteins (ABPs) are most abundant in the cytoskeleton of neurons. The function of ABPs in neurons is nucleation of actin polymerization, polymerization or depolymerization regulation, bundling of actin through crosslinking or stabilization, cargo movement along actin filaments, and anchoring of actin to other cellular components. In axons, ABP-actin interaction forms a dynamic, deep actin network, which regulates axon extension, guidance, axon branches, and synaptic structures. In dendrites, actin and ABPs are related to filopodia attenuation, spine formation, and synapse plasticity. ABP phosphorylation or mutation changes ABP-actin binding, which regulates axon or dendritic plasticity. In addition, hyperactive ABPs might also be expressed as aggregates of abnormal proteins in neurodegeneration. Those changes cause many neurological disorders. Here, we will review direct visualization of ABP and actin using various electron microscopy (EM) techniques, super resolution microscopy (SRM), and correlative light and electron microscopy (CLEM) with discussion of important ABPs in neuron. | en_US |
dc.description.sponsorship | This research was supported by the KBRI basic research program through Korea Brain Research Institute funded by Ministry of Science and ICT (20-BR-01-09), the Organelle Network Research Center (NRF-2017R1A5A1015366), and the National Research Foundation of Korea (NRF) grant funded by the Korea Government (MSIT) (No. 2018R1C1B6003436). | en_US |
dc.language.iso | en | en_US |
dc.publisher | FRONTIERS MEDIA SA | en_US |
dc.subject | electron microscopy | en_US |
dc.subject | super-resolution microscopy | en_US |
dc.subject | correlative light and electron microscopy | en_US |
dc.subject | actin binding protein | en_US |
dc.subject | actin | en_US |
dc.subject | neuronal cell | en_US |
dc.title | Direct Visualization of Actin Filaments and Actin-Binding Proteins in Neuronal Cells | en_US |
dc.type | Article | en_US |
dc.relation.volume | 8 | - |
dc.identifier.doi | 10.3389/fcell.2020.588556 | - |
dc.relation.page | 1-17 | - |
dc.relation.journal | FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY | - |
dc.contributor.googleauthor | Jung, Minkyo | - |
dc.contributor.googleauthor | Kim, Doory | - |
dc.contributor.googleauthor | Mun, Ji Young | - |
dc.relation.code | 2020050935 | - |
dc.sector.campus | S | - |
dc.sector.daehak | COLLEGE OF NATURAL SCIENCES[S] | - |
dc.sector.department | DEPARTMENT OF CHEMISTRY | - |
dc.identifier.pid | doorykim | - |
dc.identifier.orcid | https://orcid.org/0000-0002-2675-106X | - |
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