| First Author | Chanaday NL | Year | 2021 |
| Journal | Neuron | Volume | 109 |
| Issue | 8 | Pages | 1314-1332.e5 |
| PubMed ID | 33711258 | Mgi Jnum | J:332454 |
| Mgi Id | MGI:6706929 | Doi | 10.1016/j.neuron.2021.02.023 |
| Citation | Chanaday NL, et al. (2021) Presynaptic store-operated Ca(2+) entry drives excitatory spontaneous neurotransmission and augments endoplasmic reticulum stress. Neuron 109(8):1314-1332.e5 |
| abstractText | Store-operated calcium entry (SOCE) is activated by depletion of Ca(2+) from the endoplasmic reticulum (ER) and mediated by stromal interaction molecule (STIM) proteins. Here, we show that in rat and mouse hippocampal neurons, acute ER Ca(2+) depletion increases presynaptic Ca(2+) levels and glutamate release through a pathway dependent on STIM2 and the synaptic Ca(2+) sensor synaptotagmin-7 (syt7). In contrast, synaptotagmin-1 (syt1) can suppress SOCE-mediated spontaneous release, and STIM2 is required for the increase in spontaneous release seen during syt1 loss of function. We also demonstrate that chronic ER stress activates the same pathway leading to syt7-dependent potentiation of spontaneous glutamate release. During ER stress, inhibition of SOCE or syt7-driven fusion partially restored basal neurotransmission and decreased expression of pro-apoptotic markers, indicating that these processes participate in the amplification of ER-stress-related damage. Taken together, we propose that presynaptic SOCE links ER stress and augmented spontaneous neurotransmission, which may, in turn, facilitate neurodegeneration. |
