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Ultrastructure of Synaptic Connectivity within Subregions of the Suprachiasmatic Nucleus Revealed by a Genetically Encoded Tag and Serial Blockface Electron Microscopy.
Calligaro, Hugo; Shoghi, Azarin; Chen, Xinyue; Kim, Keun-Young; Yu, Hsin Liu; Khov, Brian; Finander, Benjamin; Le, Hiep; Ellisman, Mark H; Panda, Satchidananda.
Affiliation
  • Calligaro H; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Shoghi A; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Chen X; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Kim KY; Department of Neurosciences, University of California at San Diego School of Medicine, La Jolla, CA 92161.
  • Yu HL; National Center for Microscopy and Imaging Research, University of California, San Diego, La Jolla, CA 92161.
  • Khov B; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Finander B; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Le H; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Ellisman MH; Salk Institute for Biological Studies, La Jolla, CA 92037.
  • Panda S; Department of Neurosciences, University of California at San Diego School of Medicine, La Jolla, CA 92161.
eNeuro ; 10(8)2023 08.
Article in En | MEDLINE | ID: mdl-37500494
ABSTRACT
The hypothalamic suprachiasmatic nucleus (SCN) is the central circadian pacemaker in vertebrates. The SCN receives photic information exclusively through melanopsin-expressing retinal ganglion cells (mRGCs) to synchronize circadian rhythms with the environmental light cycles. The SCN is composed of two major peptidergic neuron types in the core and shell regions of the SCN. Determining how mRGCs interact with the network of synaptic connections onto and between SCN neurons is key to understand how light regulates the circadian clock and to elucidate the relevant local circuits within the SCN. To map these connections, we used a newly developed Cre-dependent electron microscopy (EM) reporter, APEX2, to label the mitochondria of mRGC axons. Serial blockface scanning electron microscopy was then used to resolve the fine 3D structure of mRGC axons and synaptic boutons in the SCN of a male mouse. The resulting maps reveal patterns of connectomic organization in the core and shell of the SCN. We show that these regions are composed of different neuronal subtypes and differ with regard to the pattern of mRGC input, as the shell receives denser mRGC synaptic input compared with the core. This finding challenges the present view that photic information coming directly from the retina is received primarily by the core region of the SCN.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Suprachiasmatic Nucleus / Circadian Clocks Limits: Animals Language: En Journal: ENeuro Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Suprachiasmatic Nucleus / Circadian Clocks Limits: Animals Language: En Journal: ENeuro Year: 2023 Document type: Article