| First Author | Mesnard CS | Year | 2022 |
| Journal | Exp Eye Res | Volume | 225 |
| Pages | 109279 | PubMed ID | 36280223 |
| Mgi Jnum | J:345105 | Mgi Id | MGI:7380097 |
| Doi | 10.1016/j.exer.2022.109279 | Citation | Mesnard CS, et al. (2022) Synaptotagmins 1 and 7 in vesicle release from rods of mouse retina. Exp Eye Res 225:109279 |
| abstractText | Synaptotagmins are the primary Ca(2+) sensors for synaptic exocytosis. Previous work suggested synaptotagmin-1 (Syt1) mediates evoked vesicle release from cone photoreceptor cells in the vertebrate retina whereas release from rods may involve another sensor in addition to Syt1. We found immunohistochemical evidence for syntaptotagmin-7 (Syt7) in mouse rod terminals and so performed electroretinograms (ERG) and single-cell recordings using mice in which Syt1 and/or Syt7 were conditionally removed from rods and/or cones. Synaptic release was measured in mouse rods by recording presynaptic anion currents activated during glutamate re-uptake and from exocytotic membrane capacitance changes. Deleting Syt1 from rods reduced glutamate release evoked by short depolarizing steps but not long steps whereas deleting Syt7 from rods reduced release evoked by long but not short steps. Deleting both sensors completely abolished depolarization-evoked release from rods. Effects of various intracellular Ca(2+) buffers showed that Syt1-mediated release from rods involves vesicles close to ribbon-associated Ca(2+) channels whereas Syt7-mediated release evoked by longer steps involves more distant release sites. Spontaneous release from rods was unaffected by eliminating Syt7. While whole animal knockout of Syt7 slightly reduced ERG b-waves and oscillatory potentials, selective elimination of Syt7 from rods had no effect on ERGs. Furthermore, eliminating Syt1 from rods and cones abolished ERG b-waves and additional elimination of Syt7 had no further effect. These results show that while Syt7 contributes to slow non-ribbon release from rods, Syt1 is the principal sensor shaping rod and cone inputs to bipolar cells in response to light flashes. |
