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Connectomics of the Octopus vulgaris vertical lobe provides insight into conserved and novel principles of a memory acquisition network.
Bidel, Flavie; Meirovitch, Yaron; Schalek, Richard Lee; Lu, Xiaotang; Pavarino, Elisa Catherine; Yang, Fuming; Peleg, Adi; Wu, Yuelong; Shomrat, Tal; Berger, Daniel Raimund; Shaked, Adi; Lichtman, Jeff William; Hochner, Binyamin.
Afiliação
  • Bidel F; Department of Neurobiology, Silberman Institute of Life Sciences, The Hebrew University, Jerusalem, Israel.
  • Meirovitch Y; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Schalek RL; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Lu X; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Pavarino EC; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Yang F; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Peleg A; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Wu Y; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Shomrat T; Faculty of Marine Sciences, Ruppin Academic Center, Michmoret, Israel.
  • Berger DR; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Shaked A; Department of Neurobiology, Silberman Institute of Life Sciences, The Hebrew University, Jerusalem, Israel.
  • Lichtman JW; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States.
  • Hochner B; Department of Neurobiology, Silberman Institute of Life Sciences, The Hebrew University, Jerusalem, Israel.
Elife ; 122023 Jul 06.
Article em En | MEDLINE | ID: mdl-37410519
Here, we present the first analysis of the connectome of a small volume of the Octopus vulgaris vertical lobe (VL), a brain structure mediating the acquisition of long-term memory in this behaviorally advanced mollusk. Serial section electron microscopy revealed new types of interneurons, cellular components of extensive modulatory systems, and multiple synaptic motifs. The sensory input to the VL is conveyed via~1.8 × 106 axons that sparsely innervate two parallel and interconnected feedforward networks formed by the two types of amacrine interneurons (AM), simple AMs (SAMs) and complex AMs (CAMs). SAMs make up 89.3% of the~25 × 106VL cells, each receiving a synaptic input from only a single input neuron on its non-bifurcating primary neurite, suggesting that each input neuron is represented in only~12 ± 3.4SAMs. This synaptic site is likely a 'memory site' as it is endowed with LTP. The CAMs, a newly described AM type, comprise 1.6% of the VL cells. Their bifurcating neurites integrate multiple inputs from the input axons and SAMs. While the SAM network appears to feedforward sparse 'memorizable' sensory representations to the VL output layer, the CAMs appear to monitor global activity and feedforward a balancing inhibition for 'sharpening' the stimulus-specific VL output. While sharing morphological and wiring features with circuits supporting associative learning in other animals, the VL has evolved a unique circuit that enables associative learning based on feedforward information flow.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Conectoma / Octopodiformes Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Israel

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Conectoma / Octopodiformes Limite: Animals Idioma: En Revista: Elife Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Israel