Key points• The mouse retina has become a key model for research on the function and dysfunction of the early stages of vision, but its photoreceptors have proven difficult to access with whole-cell recording techniques.• We have optimized the mouse retinal slice preparation to the degree required for studying photoreceptors with a reasonably high yield.• We find that single photon processing in rods is considerably more efficient than previously thought, implying a more favourable transmission at the rod-rod bipolar cell synapse.• Cones were recorded much more frequently than their numeric proportion of ∼3% allowing us to obtain direct functional evidence suggestive of rod-cone coupling in the mouse.• This study opens the way for further investigations into mammalian photoreceptor function by exploiting the powerful molecular genetic approaches available in the mouse.
AbstractResearch on photoreceptors has led to important insights into how light signals are detected and processed in the outer retina. Most information about photoreceptor function, however, comes from lower vertebrates. The large majority of mammalian studies are based on suction pipette recordings of outer segment currents, a technique that doesn't allow examination of phenomena occurring downstream of phototransduction. Only a small number of whole-cell recordings have been made, mainly in the macaque. Due to the growing importance of the mouse in vision research, we have optimized a retinal slice preparation that allows the reliable collection of perforated-patch recordings from light responding rods and cones. Unexpectedly, the frequency of cone recordings was much higher than their numeric proportion of ∼3%. This allowed us to obtain direct functional evidence suggestive of rod-cone coupling in the mouse. Moreover, rods had considerably larger single photon responses than previously published for mammals (3.44 mV, SD 1.37, n = 19 at 24 • C; 2.46 mV, SD 1.08, n = 10 at 36 • C), and a relatively high signal/noise ratio (6.4, SD 1.8 at 24• C; 6.8, SD 2.8 at 36• C). Both findings imply a more favourable transmission at the rod-rod bipolar cell synapse. Accordingly, relatively few photoisomerizations were sufficient to elicit a half-maximal response (6.7, SD 2.7, n = 5 at 24• C; 10.6, SD 1.7, n = 3 at 36 • C), leading to a narrow linear response range. Our study demonstrates new features of mammalian photoreceptors and opens the way for further investigations into photoreceptor function using retinas from mutant mouse models.