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. 2018 Sep 11;7:e34997. doi: 10.7554/eLife.34997

Figure 7. Models summarizing findings of this work.

Figure 7.

(A) AS MNs asymmetrically regulate dorso-ventral bending during forward and backward locomotion, by excitatory chemical transmission to dorsal muscles and ventral GABAergic VD MNs, thus causing ventral inhibition. Interconnections (arrows, chemical synapses; curved lines, electrical synapses; thickness of lines indicates relative synapse number as an approximation of synaptic strength; color shade represents strength of functional connections measured in this work) of AS MNs and their other synaptic partners,that is the PINs AVB and AVA, via both chemical synapses from the PINs and (reciprocal) electrical synapses from AS MNs are also shown. Data in this work suggest (chemical) excitatory regulation of AS MNs by AVA and AVB during forward and backward locomotion, respectively, and reciprocal electrical regulation of AVA by AS MNs. (B) Interconnections and functional roles of AS MNs and other VNC MNs during the propagation of the undulatory wave along the body. Depolarization (which could be initiated by AVB, not shown here, or by proprioceptive feedback from the adjacent body segment) of AS MNs causes contraction of the dorsal BWMs and simultaneous relaxation of ventral BWMs through the excitation of VD MNs. This phase is followed by contraction of ventral BWMs, e.g. through the electric coupling of AS and VA MNs, and relaxation of the dorsal BWMs through VD-DD electrical coupling or VA-DD chemical synapses. Cholinergic (orange) and GABAergic (blue) cell types are indicated. Antero-posterior localization of cell bodies and connectivity to other cell types are arbitrary.