Receptor architecture of the macaque lateral geniculate nucleus.
Overview
- Faculty of Design and Architecture, Nagoya City University, 2-1-10, Kita Chikusa, Chikusa-ku, Nagoya, 464−0083 Japan
- Division and Sensory and Cognitive Brain Mapping, Department of System Neuroscience, National Institute for Physiological Sciences, Okazaki, 444–8585 Japan
- Japan Society for the Promotion of Science, Tokyo, 102−0083 Japan
- Laboratory for Imagination and Executive Functions, RIKEN Center for Brain Science, Wako, 351−0198 Japan
- C. & O. Vogt Institute of Brain Research, Heinrich-Heine University Düsseldorf, 40225 Düsseldorf, Germany
- Research Centre Jülich, Institute of Neuroscience and Medicine (INM-1), 52425 Jülich, Germany
- Department of Psychology, School of Public Policy and Management, Nanchang University, Nanchang, 330031 China
- The Graduate Institute of Advanced Studies, SOKENDAI, Hayama, 240−0115 Japan
- Core for Spin Life Sciences, Okazaki Collaborative Platform, National Institutes of Natural Sciences, Okazaki, 444–8585 Japan
Abstract
The lateral geniculate nucleus (LGN) is a key thalamic nucleus in the primate visual system that relays visual information from the retina to cortical visual areas. While functional and microanatomical characteristics of the LGN and its layers have been extensively studied, previous investigations on its receptor architecture have been restricted to a small subset of neurotransmitter receptors. To characterise the receptor architecture of the macaque LGN in greater detail, we analysed in vitro autoradiography data to quantify the density of 15 neurotransmitter receptors at the sublayer level, thus improving our understanding of the molecular architecture supporting primate visual function. For comparison, we also determined the densities of these receptors in the primary visual cortex (V1) at a laminar level. Though comparable in shape, the receptor fingeprints of magnocellular layers were larger than those of parvocellular layers. In contrast, receptor fingerprints of cytoarchitectonic layers in V1 differed in both shape and size. Ionotropic/
Supplementary Information: The online version contains supplementary material available at 10.1007/
Reproduced under the paper's license (CC BY), from the paper cited above.
Code
The paper links to its data, not to its authors' code: see the Data section.
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Data
Datasets cited
- doi:10.25493/
vs8j-v0e , at the source; found in “Data availability”
Data availability
The original data, including numbers of receptor densities used for generating figures shown in this manuscript, are provided in the Supplementary Tables (Tables S1 and S2) and have been made publicly available via the EBRAINS platform (https://
Reproduced under the paper's license (CC BY), from the paper cited above.
Versions
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Version 2, 28 September 2026
- Publisher: n/a → Springer Science+Business Media
Version 1, 28 September 2026: the first record
Recorded: type, language, journal, volume, issue, pages, dates, 7 authors, 6 keywords, 9 MeSH terms, 1 funder, 116 references.
Cite
This paper
Saito, M., Rapan, L., Niu, M., Zhao, L., Tsujimura, S.-i., Takemura, H., & Palomero-Gallagher, N. (2026). Receptor architecture of the macaque lateral geniculate nucleus. Brain structure & function, 231(5), 67. https://
BibTeX
@article{saito2026recept
author = {Saito, Marina and Rapan, Lucija and Niu, Meiqi and Zhao, Ling and Tsujimura, Sei-ichi and Takemura, Hiromasa and Palomero-Gallagher, Nicola},
title = {{Receptor architecture of the macaque lateral geniculate nucleus}},
journal = {Brain structure \& function},
year = {2026},
month = may,
volume = {231},
number = {5},
pages = {67},
publisher = {Springer Science+Business Media},
issn = {1863-2653},
doi = {10.1007/
url = {https://
pmid = {42154062},
pmcid = {PMC13186819}
}
RIS
TY - JOUR
AU - Saito, Marina
AU - Rapan, Lucija
AU - Niu, Meiqi
AU - Zhao, Ling
AU - Tsujimura, Sei-ichi
AU - Takemura, Hiromasa
AU - Palomero-Gallagher, Nicola
TI - Receptor architecture of the macaque lateral geniculate nucleus
T2 - Brain structure & function
J2 - Brain Struct Funct
PY - 2026
DA - 2026/
VL - 231
IS - 5
SP - 67
SN - 1863-2653
PB - Springer Science+Business Media
DO - 10.1007/
UR - https://
LA - en
ER -
CSL-JSON
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