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Chen, A. Q.

Publications and source records attributed to Chen, A. Q..

2 recordsLinked to original sources

Cryo-EM structures of insect IRs reveal the structural adaptations of a glutamate receptor ancestor for environmental sensing

Ionotropic receptors (IRs) are an ancient, massively expanded family of sensory ion channels that mediate chemical, thermal, and hygrosensory detection across invertebrates. Derived from synaptic ionotropic glutamate receptors (iGluRs), IRs achieve this diverse tuning by assembling conserved co-receptor subunits with highly divergent tuning subunits into obligate heteromers. To understand how this architecture arose from a glutamate receptor ancestor we report cryo-EM structures of three insect IR complexes spanning the major functional subfamilies: IR8a/IR75b, IR25a/IR76b, and IR25a/IR93a/IR40a. All IR complexes retain the tiered iGluR architecture but adopt a distinctive splayed, non-swapped architecture that our phylogenetic reconstructions relate to a sister branch of glutamate delta (GluD) receptors. Our structures reveal a novel, co-receptor-specific helical beam feature that dictates stoichiometry by interlocking the co-receptors and separating the tuning subunits, at the cost of abolishing ligand binding in co-receptors. Comparison of IR8a- and IR25a- containing complexes further illuminates the structural basis of subfamily specificity yielding a predictive code of co-receptor assembly. Lastly, we identify IR-specific coupling mechanisms between the gating machineries of tuning and co-receptor subunits, offering a model for the cooperative gating of IRs. These analyses illuminate how an ancient synaptic receptor was architecturally remodeled into a multimodal family of sensory receptors that drive critical behaviors across invertebrates.

neuroscience↗

Cellular Mechanisms Underlying Embryonic Retinal Waves

Spontaneous activity is a hallmark of developing neural systems. In the retina, spontaneous activity comes in the form of retinal waves, comprised of three stages persisting from embryonic day 16 (E16) to eye opening at postnatal day 14 (P14). Though postnatal retinal waves have been well characterized, little is known about the spatiotemporal properties or the mechanisms mediating embryonic retinal waves, designated Stage 1 waves. Using a custom-built macroscope to record spontaneous calcium transients from whole embryonic retinas, we show that Stage 1 waves are initiated at several locations across the retina and propagate across finite regions of a broad range of areas. A gap junction antagonist, meclofenamic acid, reduced the frequency and size of Stage 1 waves but did not abolish them. The general nAChR antagonist, hexamethonium blocked Stage 1 waves, while they persisted in the presence of 4{beta}2 nAChR antagonist dihydro-{beta}-erythroidine, indicating that the spatiotemporal properties of Stage 1 waves are mediated by a complex circuitry involving subtypes of nAChRs and gap junctions. Stage 1 waves in mice lacking the {beta}2 subunit of the nAChRs ({beta}2-nAChR-KO) were reduced, but in contrast to WT mice, they persisted in the hexamethonium and were completely blocked by meclofenamic acid. To assay the impact of Stage 1 waves on retinal development, we compared the spatial distribution of a subtype of retinal ganglion cells, intrinsically photosensitive retinal ganglion cells (ipRGCs) in WT and {beta}2-nAChR-KO mice. We found that the developmental decrease of ipRGC density is preserved between WT and {beta}2-nAChR-KO mice, indicating that processes regulating ipRGC distribution are not influenced by spontaneous activity.

neuroscience↗