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A biologically inspired repair mechanism for neuronal reconstructions with a focus on human dendrites.
Groden, Moritz; Moessinger, Hannah M; Schaffran, Barbara; DeFelipe, Javier; Benavides-Piccione, Ruth; Cuntz, Hermann; Jedlicka, Peter.
Afiliación
  • Groden M; 3R Computer-Based Modelling, Faculty of Medicine, ICAR3R, Justus Liebig University Giessen, Giessen, Germany.
  • Moessinger HM; Ernst Strüngmann Institute (ESI) for Neuroscience in cooperation with the Max Planck Society, Frankfurt am Main, Germany.
  • Schaffran B; Ernst Strüngmann Institute (ESI) for Neuroscience in cooperation with the Max Planck Society, Frankfurt am Main, Germany.
  • DeFelipe J; Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
  • Benavides-Piccione R; Laboratorio Cajal de Circuitos Corticales (CTB), Universidad Politécnica de Madrid, Spain.
  • Cuntz H; Instituto Cajal (CSIC), Madrid, Spain.
  • Jedlicka P; Laboratorio Cajal de Circuitos Corticales (CTB), Universidad Politécnica de Madrid, Spain.
PLoS Comput Biol ; 20(2): e1011267, 2024 Feb.
Article en En | MEDLINE | ID: mdl-38394339
ABSTRACT
Investigating and modelling the functionality of human neurons remains challenging due to the technical limitations, resulting in scarce and incomplete 3D anatomical reconstructions. Here we used a morphological modelling approach based on optimal wiring to repair the parts of a dendritic morphology that were lost due to incomplete tissue samples. In Drosophila, where dendritic regrowth has been studied experimentally using laser ablation, we found that modelling the regrowth reproduced a bimodal distribution between regeneration of cut branches and invasion by neighbouring branches. Interestingly, our repair model followed growth rules similar to those for the generation of a new dendritic tree. To generalise the repair algorithm from Drosophila to mammalian neurons, we artificially sectioned reconstructed dendrites from mouse and human hippocampal pyramidal cell morphologies, and showed that the regrown dendrites were morphologically similar to the original ones. Furthermore, we were able to restore their electrophysiological functionality, as evidenced by the recovery of their firing behaviour. Importantly, we show that such repairs also apply to other neuron types including hippocampal granule cells and cerebellar Purkinje cells. We then extrapolated the repair to incomplete human CA1 pyramidal neurons, where the anatomical boundaries of the particular brain areas innervated by the neurons in question were known. Interestingly, the repair of incomplete human dendrites helped to simulate the recently observed increased synaptic thresholds for dendritic NMDA spikes in human versus mouse dendrites. To make the repair tool available to the neuroscience community, we have developed an intuitive and simple graphical user interface (GUI), which is available in the TREES toolbox (www.treestoolbox.org).
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dendritas / Neuronas Límite: Animals / Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dendritas / Neuronas Límite: Animals / Humans Idioma: En Revista: PLoS Comput Biol Asunto de la revista: BIOLOGIA / INFORMATICA MEDICA Año: 2024 Tipo del documento: Article País de afiliación: Alemania