L1CAM/Neuroglian controls the axon–axon interactions establishing layered and lobular mushroom body architecture
Autor: | Eliza Moreno, Dominique Siegenthaler, Eva-Maria Enneking, Jan Pielage |
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Jazyk: | angličtina |
Rok vydání: | 2015 |
Předmět: |
Ankyrins
L1 Cerebral Peduncle Moesin Cell Adhesion Molecules Neuronal Neural Cell Adhesion Molecule L1 Biology Article Cell Line Memory medicine Cell Adhesion Animals Drosophila Proteins Axon Cell adhesion Research Articles Mushroom Bodies Cell Aggregation Microfilament Proteins Gene Expression Regulation Developmental Cell Biology Anatomy Cell aggregation Axons Cell biology Protein Structure Tertiary medicine.anatomical_structure Drosophila melanogaster nervous system Mushroom bodies Axon guidance Intracellular |
Zdroj: | The Journal of Cell Biology |
ISSN: | 1540-8140 0021-9525 |
Popis: | Targeted domain-specific mutations and cell type–specific rescue experiments show that L1CAM/Neuroglian is required for axon–axon interactions and yield insights into the cellular mechanisms controlling establishment of the complex mushroom body architecture. The establishment of neuronal circuits depends on the guidance of axons both along and in between axonal populations of different identity; however, the molecular principles controlling axon–axon interactions in vivo remain largely elusive. We demonstrate that the Drosophila melanogaster L1CAM homologue Neuroglian mediates adhesion between functionally distinct mushroom body axon populations to enforce and control appropriate projections into distinct axonal layers and lobes essential for olfactory learning and memory. We addressed the regulatory mechanisms controlling homophilic Neuroglian-mediated cell adhesion by analyzing targeted mutations of extra- and intracellular Neuroglian domains in combination with cell type–specific rescue assays in vivo. We demonstrate independent and cooperative domain requirements: intercalating growth depends on homophilic adhesion mediated by extracellular Ig domains. For functional cluster formation, intracellular Ankyrin2 association is sufficient on one side of the trans-axonal complex whereas Moesin association is likely required simultaneously in both interacting axonal populations. Together, our results provide novel mechanistic insights into cell adhesion molecule–mediated axon–axon interactions that enable precise assembly of complex neuronal circuits. |
Databáze: | OpenAIRE |
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