1
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Dynamic instability of dendrite tips generates the highly branched morphologies of sensory neurons

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The highly ramified arbors of neuronal dendrites provide the substrate for the high connectivity and computational power of the brain. Altered dendritic morphology is associated with neuronal diseases. Many molecules have been shown to play crucial roles in shaping and maintaining dendrite morphology. However, the underlying principles by which molecular interactions generate branched morphologies are not understood. To elucidate these principles, we visualized the growth of dendrites throughout larval development of Drosophila sensory neurons and found that the tips of dendrites undergo dynamic instability, transitioning rapidly and stochastically between growing, shrinking, and paused states. By incorporating these measured dynamics into an agent-based computational model, we showed that the complex and highly variable dendritic morphologies of these cells are a consequence of the stochastic dynamics of their dendrite tips. These principles may generalize to branching of other neuronal cell types, as well as to branching at the subcellular and tissue levels.

          Abstract

          Abstract

          The complex and highly variable dendritic morphologies emerge from the stochastic dynamics of dendrite tips.

          Related collections

          Most cited references72

          • Record: found
          • Abstract: not found
          • Article: not found

          Novel Type of Phase Transition in a System of Self-Driven Particles

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Cellular motility driven by assembly and disassembly of actin filaments.

            Motile cells extend a leading edge by assembling a branched network of actin filaments that produces physical force as the polymers grow beneath the plasma membrane. A core set of proteins including actin, Arp2/3 complex, profilin, capping protein, and ADF/cofilin can reconstitute the process in vitro, and mathematical models of the constituent reactions predict the rate of motion. Signaling pathways converging on WASp/Scar proteins regulate the activity of Arp2/3 complex, which mediates the initiation of new filaments as branches on preexisting filaments. After a brief spurt of growth, capping protein terminates the elongation of the filaments. After filaments have aged by hydrolysis of their bound ATP and dissociation of the gamma phosphate, ADF/cofilin proteins promote debranching and depolymerization. Profilin catalyzes the exchange of ADP for ATP, refilling the pool of ATP-actin monomers bound to profilin, ready for elongation.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Dynamic instability of microtubule growth.

              We report here that microtubules in vitro coexist in growing and shrinking populations which interconvert rather infrequently. This dynamic instability is a general property of microtubules and may be fundamental in explaining cellular microtubule organization.
                Bookmark

                Author and article information

                Contributors
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: InvestigationRole: MethodologyRole: Project administrationRole: ValidationRole: VisualizationRole: Writing - original draft
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: InvestigationRole: MethodologyRole: Project administrationRole: SoftwareRole: ValidationRole: VisualizationRole: Writing - original draft
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: MethodologyRole: SoftwareRole: SupervisionRole: Validation
                Role: ConceptualizationRole: Formal analysisRole: MethodologyRole: Writing - original draft
                Role: Investigation
                Role: ConceptualizationRole: Data curationRole: Formal analysisRole: Funding acquisitionRole: MethodologyRole: Project administrationRole: ResourcesRole: SupervisionRole: ValidationRole: VisualizationRole: Writing - original draftRole: Writing - review & editing
                Journal
                Sci Adv
                Sci Adv
                sciadv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                June 2022
                29 June 2022
                : 8
                : 26
                : eabn0080
                Affiliations
                [1 ]Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA.
                [2 ]Department of Physics, Yale University, New Haven, CT 06511, USA.
                [3 ]IBM T.J. Watson Research Center, Yorktown Heights, NY 10598, USA.
                [4 ]Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, 100084 Beijing, China.
                [5 ]Quantitative Biology Institute, Yale University, New Haven, CT 06511, USA.
                Author notes
                [* ]Corresponding author. Email: joe.howard@ 123456yale.edu
                [†]

                These authors contributed equally to this work.

                Author information
                https://orcid.org/0000-0002-5665-8157
                https://orcid.org/0000-0002-5826-5891
                https://orcid.org/0000-0002-7437-4801
                https://orcid.org/0000-0001-7915-8094
                Article
                abn0080
                10.1126/sciadv.abn0080
                9242452
                35767611
                771bca82-d464-4c36-83f1-92b319703ebf
                Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 28 October 2021
                : 12 May 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100000002, National Institutes of Health;
                Award ID: R01 NS118884
                Funded by: FundRef http://dx.doi.org/10.13039/100000052, NIH Office of the Director;
                Award ID: DP1 MH110065
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 31671389
                Funded by: Fonds de Recherch du Quebec Nature et Technologies;
                Categories
                Research Article
                Biomedicine and Life Sciences
                SciAdv r-articles
                Biophysics
                Developmental Biology
                Developmental Biology
                Custom metadata
                Nicole Falcasantos

                Comments

                Comment on this article