Neurotransmitter release progressively desynchronizes in induced human neurons during synapse maturation and aging

Cell Rep. 2023 Feb 28;42(2):112042. doi: 10.1016/j.celrep.2023.112042. Epub 2023 Jan 25.

Abstract

Rapid release of neurotransmitters in synchrony with action potentials is considered a key hardwired property of synapses. Here, in glutamatergic synapses formed between induced human neurons, we show that action potential-dependent neurotransmitter release becomes progressively desynchronized as synapses mature and age. In this solely excitatory network, the emergence of NMDAR-mediated transmission elicits endoplasmic reticulum (ER) stress leading to downregulation of key presynaptic molecules, synaptotagmin-1 and cysteine string protein α, that synchronize neurotransmitter release. The emergence of asynchronous release with neuronal maturity and subsequent aging is maintained by the high-affinity Ca2+ sensor synaptotagmin-7 and suppressed by the introduction of GABAergic transmission into the network, inhibition of NMDARs, and ER stress. These results suggest that long-term disruption of excitation-inhibition balance affects the synchrony of excitatory neurotransmission in human synapses.

Keywords: CP: Neuroscience; asynchronous release; human synapse; synaptic aging; synaptotagmin.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aging
  • Calcium / metabolism
  • Humans
  • Neurons* / metabolism
  • Neurotransmitter Agents / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Synapses / metabolism
  • Synaptic Transmission* / physiology

Substances

  • Neurotransmitter Agents
  • Receptors, N-Methyl-D-Aspartate
  • Calcium