Innexin expression and localization in the Drosophila antenna indicate gap junction or hemichannel involvement in antennal chemosensory sensilla.

Autor: Prelic S; Dept. Evolutionary Neuroethology, Max Planck Institute for Chemical Ecology, Jena, Germany., Keesey IW; Dept. Evolutionary Neuroethology, Max Planck Institute for Chemical Ecology, Jena, Germany., Lavista-Llanos S; Dept. Evolutionary Neuroethology, Max Planck Institute for Chemical Ecology, Jena, Germany., Hansson BS; Dept. Evolutionary Neuroethology, Max Planck Institute for Chemical Ecology, Jena, Germany., Wicher D; Dept. Evolutionary Neuroethology, Max Planck Institute for Chemical Ecology, Jena, Germany. dwicher@ice.mpg.de.
Jazyk: angličtina
Zdroj: Cell and tissue research [Cell Tissue Res] 2024 Oct; Vol. 398 (1), pp. 35-62. Date of Electronic Publication: 2024 Aug 23.
DOI: 10.1007/s00441-024-03909-3
Abstrakt: Odor detection in insects is largely mediated by structures on antennae called sensilla, which feature a strongly conserved architecture and repertoire of olfactory sensory neurons (OSNs) and various support cell types. In Drosophila, OSNs are tightly apposed to supporting cells, whose connection with neurons and functional roles in odor detection remain unclear. Coupling mechanisms between these neuronal and non-neuronal cell types have been suggested based on morphological observations, concomitant physiological activity during odor stimulation, and known interactions that occur in other chemosensory systems. For instance, it is not known whether cell-cell coupling via gap junctions between OSNs and neighboring cells exists, or whether hemichannels interconnect cellular and extracellular sensillum compartments. Here, we show that innexins, which form hemichannels and gap junctions in invertebrates, are abundantly expressed in adult drosophilid antennae. By surveying antennal transcriptomes and performing various immunohistochemical stainings in antennal tissues, we discover innexin-specific patterns of expression and localization, with a majority of innexins strongly localizing to glial and non-neuronal cells, likely support and epithelial cells. Finally, by injecting gap junction-permeable dye into a pre-identified sensillum, we observe no dye coupling between neuronal and non-neuronal cells. Together with evidence of non-neuronal innexin localization, we conclude that innexins likely do not conjoin neurons to support cells, but that junctions and hemichannels may instead couple support cells among each other or to their shared sensillum lymph to achieve synchronous activity. We discuss how coupling of sensillum microenvironments or compartments may potentially contribute to facilitate chemosensory functions of odor sensing and sensillum homeostasis.
(© 2024. The Author(s).)
Databáze: MEDLINE
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