4.7 Article

Differentiation and Characterization of Excitatory and Inhibitory Synapses by Cryo-electron Tomography and Correlative Microscopy

期刊

JOURNAL OF NEUROSCIENCE
卷 38, 期 6, 页码 1493-1510

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1548-17.2017

关键词

correlative light and electron microscopy; cryo-electron tomography; neurotransmitter receptor; postsynaptic density; synaptic ultrastructure; synaptic vesicle

资金

  1. Chinese Academy of Sciences [XDB02050000]
  2. National Natural Science Foundation of China [30725017, 91232722, 31070935]
  3. China Ministry of Science and Technology [2009CB941300]
  4. National Institutes of Health (NIH) [GM071940]
  5. NIH [S10RR23057, S10OD018111]
  6. National Science Foundation [DBI-133813]
  7. BBSRC [BB/S003339/1] Funding Source: UKRI

向作者/读者索取更多资源

As key functional units in neural circuits, different types of neuronal synapses play distinct roles in brain information processing, learning, and memory. Synaptic abnormalities are believed to underlie various neurological and psychiatric disorders. Here, by combining cryo-electron tomography and cryo-correlative light and electron microscopy, we distinguished intact excitatory and inhibitory synapses of cultured hippocampal neurons, and visualized the in situ 3D organization of synaptic organelles and macromolecules in their native state. Quantitative analyses of >100 synaptic tomograms reveal that excitatory synapses contain a mesh-like postsynaptic density (PSD) with thickness ranging from 20 to 50 nm. In contrast, the PSD in inhibitory synapses assumes a thin sheet-like structure similar to 12 nm from the postsynaptic membrane. On the presynaptic side, spherical synaptic vesicles (SVs) of 25-60 nm diameter and discus-shaped ellipsoidal SVs of various sizes coexist in both synaptic types, with more ellipsoidal ones in inhibitory synapses. High-resolution tomograms obtained using a Volta phase plate and electron filtering and counting reveal glutamate receptor-like and GABAA receptor-like structures that interact with putative scaffolding and adhesion molecules, reflecting details of receptor anchoring and PSD organization. These results provide an updated view of the ultrastructure of excitatory and inhibitory synapses, and demonstrate the potential of our approach to gain insight into the organizational principles of cellular architecture underlying distinct synaptic functions.

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