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Celebrating the Birthday of AMPA Receptor Nanodomains: Illuminating the Nanoscale Organization of Excitatory Synapses with 10 Nanocandles

Research output: Contribution to JournalArticleAcademicpeer-review

Abstract

A decade ago, in 2013, and over the course of 4 summer months, three separate observations were reported that each shed light independently on a new molecular organization that fundamentally reshaped our perception of excitatory synaptic transmission (Fukata et al., 2013; MacGillavry et al., 2013; Nair et al., 2013). This discovery unveiled an intricate arrangement of AMPA-type glutamate receptors and their principal scaffolding protein PSD-95, at synapses. This breakthrough was made possible, thanks to advanced super-resolution imaging techniques. It fundamentally changed our understanding of excitatory synaptic architecture and paved the way for a brand-new area of research. In this Progressions article, the primary investigators of the nanoscale organization of synapses have come together to chronicle the tale of their discovery. We recount the initial inquiry that prompted our research, the preceding studies that inspired our work, the technical obstacles that were encountered, and the breakthroughs that were made in the subsequent decade in the realm of nanoscale synaptic transmission. We review the new discoveries made possible by the democratization of super-resolution imaging techniques in the field of excitatory synaptic physiology and architecture, first by the extension to other glutamate receptors and to presynaptic proteins and then by the notion of trans-synaptic organization. After describing the organizational modifications occurring in various pathologies, we discuss briefly the latest technical developments made possible by super-resolution imaging and emerging concepts in synaptic physiology.
Original languageEnglish
Article numbere2104232024
Pages (from-to)1-18
Number of pages18
JournalJournal of Neuroscience
Volume44
Issue number23
DOIs
Publication statusPublished - 5 Jun 2024
Externally publishedYes

Funding

E.H. was supported by funding from the Minist\u00E8re de l\u2019Enseignement Sup\u00E9rieur et de la Recherche [ANR SyTune ANR-21-CE37-0010 and SytGAP ANR-21-NEUC-0003 and E.U. Horizon-Hlth-2022-Disease-06 (101080580)] Centre National de la Recherche Scientifique. Y.F. was supported by grants from the Ministry of Education, Culture, Sports, Science and Technology (21K19390 and 22H02723), the Japan Agency for Medical Research and Development (JP23wm0525022), and the Takeda Science Foundation. M.F. was supported by grants from the Ministry of Education, Culture, Sports, Science and Technology (23H00374, 23H04243, and 23K18228), the Japan Agency for Medical Research and Development (JP23ek0109649), and the Takeda Science Foundation. D.N. was supported by the Science and Engineering Research Board-Core Research Grant (CRG/2019/006899 and CRG/2022/002726), STARS program grant CBR-FABRIC (Funding for Aging Brain Research & Innovation Collaborations), and DBT-IISc partnership program. H.D.M. was supported by the Dutch Research Council (OCENW.KLEIN.163 and OCENW.M.21.285) and Alzheimer NL (WE.03-2022-09). We thank all scientists for the century of research that inspires us day in day out, and we apologize to those whose work could not be cited owing to space constraints.

FundersFunder number
DBT-IISc
Centre National de la Recherche Scientifique
CBR-FABRIC
Ministère de l'Enseignement Supérieur et de la Recherche
???publication-publication-funding-organisation-not-added???ANR-21-NEUC-0003
Japan Agency for Medical Research and DevelopmentJP23wm0525022
Nederlandse Organisatie voor Wetenschappelijk OnderzoekOCENW.KLEIN.163, OCENW.M.21.285
Takeda Science FoundationJP23ek0109649, 23H04243, 23K18228, 23H00374
Ministry of Education, Culture, Sports, Science and Technology21K19390, 22H02723
ANR-21-CE37-0010101080580
Science and Engineering Research BoardCRG/2019/006899, CRG/2022/002726
Alzheimer NLWE.03-2022-09

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