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Lanoizelet, M.

Publications and source records attributed to Lanoizelet, M..

2 recordsLinked to original sources

Novel dopaminergic neurotransmission in the Octopus visual system

Octopus vulgaris, the common octopus, has a complex brain that evolved independently from that of vertebrates, raising the possibility that it may be built using novel circuit motifs or non-canonical neurochemistry. Through systematic characterization of octopus ligand-gated ion channel genes, we identified novel ionotropic receptors for two neurotransmitters, dopamine and acetylcholine, that play key roles in visual circuits. One of these, DopC1, encodes a dopamine-gated cation channel expressed in deeper layers of the optic lobe (inner granular layer and medulla). A second, AChRB1, encodes an acetylcholine-gated anion channel expressed in photoreceptors and dopaminergic outer granular layer neurons. Dopamine drives excitation, particularly in deeper, DopC1 enriched layers, and thereby may play an important role in feed-forward excitation, whereas acetylcholine evokes inhibition, possibly mediating negative feedback from deeper layers. The octopus visual system thus shows fundamental differences in both neurochemistry and wiring compared to mammals, implying distinct mechanisms of visual information processing.

neuroscience↗

Analysis of a shark reveals ancient habenular asymmetries in gnathostomes and points to Wnt regulation as a driving force in their diversification

The origin of left-right asymmetries in the vertebrate habenula remains largely unknown. Using a transcriptomic approach, we show that in a cartilaginous fish, the catshark Scyliorhinus canicula, habenulae exhibit marked asymmetries both in their medial and their lateral component. Comparisons across gnathostomes suggest that asymmetries in the catshark lateral habenulae reflect an ancestral gnathostome trait, independently lost in tetrapods and neopterygians. Analysis of the mechanisms underlying their formation highlights an essential role of Wnt signaling. Wnt activity is submitted to a dynamic, asymmetric regulation during habenula development, with a Nodal dependent left repression at a stage when precursors for lateral habenulae have exited cell cycles. Pharmacological treatments during this time window reveal that Wnt signaling promotes lateral right neuronal identities in the right lateral habenula, while its repression by Nodal in the left one promotes lateral left neuronal identities. Based on comparisons with the zebrafish and the mouse, we propose that habenular asymmetry formation and diversification in gnathostomes involve the same developmental logic, relying on a conserved temporal regulation of neurogenesis, shaping neuronal identities on both sides, and its modification by a dynamic Wnt activity, right-restricted in the ancestral state and prone to variations in time and space during evolution.

developmental biology↗