Transmission Of Visual Signals Research Articles

Cryo-EM structure of human class C orphan GPCR GPR179 involved in visual processing

GPR179, an orphan class C GPCR, is expressed at the dendritic tips of ON-bipolar cells in the retina. It plays a pivotal role in the initial synaptic transmission of visual signals from photoreceptors, and its deficiency is known to be the cause of complete congenital stationary night blindness. Here, we present the cryo-electron microscopy structure of human GPR179. Notably, the transmembrane domain (TMD) of GPR179 forms a homodimer through the TM1/7 interface with a single inter-protomer disulfide bond, adopting a noncanonical dimerization mode. Furthermore, the TMD dimer exhibits architecture well-suited for the highly curved membrane of the dendritic tip and distinct from the flat membrane arrangement observed in other class C GPCR dimers. Our structure reveals unique structural features of GPR179 TMD, setting it apart from other class C GPCRs. These findings provide a foundation for understanding signal transduction through GPR179 in visual processing and offers insights into the underlying causes of ocular diseases.

An integrated textile of electrical signal sensing with visual indicators and energy supply for perspiration management

Recent advances in wearable electronics have enabled the development of sweat sensors providing valuable information for healthcare monitoring. However, the limitations of sweat sensors are excessive dependence on external detection systems, the impossible to real-time visual signal transmission, and inadequate perspiration management. Herein, a single- and double-layer interwoven fabric (SDIF) is designed to achieve indicators of color visualization with an output of electrical signal and energy supply. After absorption of electrolyte, the SDIF can be rapidly activated, connected with the concentration, infiltrated volume, and environmental parameters, and the variational color of SDIF can provide visual indicators. The one tissue cycle of SDIF with three-weft intervals maintains a stable output voltage of ≈1.0 V, conducted by twisting, folding, dynamic bending, and reusing. Moreover, serial tissue cycles can be woven into large fabrics by connecting in series and parallel configurations for energy supply. The developed SDIF with an interweaving structural design using industrial-producible weaving technology provides the functionality of sweat adsorption and transportation, monitoring by recognition of color, and electrical signals to improve perspiration management.

Fixational Eye Movements Enhance the Precision of Visual Information Transmitted by the Primate Retina.

Fixational eye movements alter the number and timing of spikes transmitted from the retina to the brain, but whether these changes enhance or degrade the retinal signal is unclear. To quantify this, we developed a Bayesian method for reconstructing natural images from the recorded spikes of hundreds of retinal ganglion cells (RGCs) in the macaque retina (male), combining a likelihood model for RGC light responses with the natural image prior implicitly embedded in an artificial neural network optimized for denoising. The method matched or surpassed the performance of previous reconstruction algorithms, and provides an interpretable framework for characterizing the retinal signal. Reconstructions were improved with artificial stimulus jitter that emulated fixational eye movements, even when the eye movement trajectory was assumed to be unknown and had to be inferred from retinal spikes. Reconstructions were degraded by small artificial perturbations of spike times, revealing more precise temporal encoding than suggested by previous studies. Finally, reconstructions were substantially degraded when derived from a model that ignored cell-to-cell interactions, indicating the importance of stimulus-evoked correlations. Thus, fixational eye movements enhance the precision of the retinal representation.

Tunable thermoresponsive and stretchable hydrogel sensor based on hydroxypropyl cellulose for human motion/health detection, visual signal transmission and information encryption

Thermoresponsive hydrogels can be used as smart flexible sensors. However, the design and facile preparation of multifunctional thermoresponsive hydrogel sensors still face great challenges. Herein, a tunable thermoresponsive, thermochromic and stretchable poly(2-hydroxypropyl acrylate-co-acrylamide) (P(HPA-co-AM))/hydroxypropyl cellulose (HPC)/lithium chloride (LiCl) hydrogel with the networks constructed from non-covalent interaction was fabricated by photopolymerization. PHPA exhibits excellent thermoresponsiveness. HPC endows the hydrogel with outstanding mechanical performance and enhanced temperature-sensitivity. LiCl not only provides good conductivity, but also regulates the lower critical solution temperature (LCST) of the hydrogel. The hydrogel shows tensile strength up to 300 kPa and maximum strain up to 790 %. The LCST value of the hydrogel can be adjusted from 38 to 75 °C. Therefore, the thermoresponsive conductive hydrogel can realize the information encryption, and be used as sensor through strain and temperature changes in the external environment to realize the motion and health detection, and visual signal transmission. This work is expected to provide ideas for the next generation of smart multifunctional electronic skin and information encryption device.

A Contour Detection Method Based on the Projective Coding Model of the Visual Cortex Information Flow

Based on the information flow partition projection characteristics of P-type and M-type ganglion cells (referred to as P cells and M cells) and the neural sparse coding mechanism, this paper proposed a new method for image contour detection. First, we considered the difference between M cells and P cells in detail sensitivity and the information transmission of different visual signals. The parallel visual pathway was constructed to simulate the pre-level characteristics of the V1 layer to obtain the primary contour response. Then, we introduced the orientation sensitivity and stimulus response difference of the visual receptive field to construct the visual information difference enhancement model. In consideration of the visual attention mechanism, we proposed an adaptive size sparse coding network model that simulates the pre-level characteristics of the V4 layer to intelligently focus the target contour features. At the same time, de-redundancy was performed to obtain the fine feature image. Finally, the hierarchical information feedback fusion was built, and the fine feature image was used to correct the primary contour response to obtain complete contour detection results. Taking the BSDS500 dataset as experimental objects, the results showed that the proposed method exhibits an effective trade-off between contour extraction and texture suppression.

Diacylglycerol Signaling in Retinal Ganglion Cells.

With impaired retinal ganglion cell (RGC) function and eventual RGC death, there is a heightened risk of experiencing glaucoma-induced blindness or other optic neuropathies. Poor RGC efficiency leads to limited transmission of visual signals between the retina and the brain by RGC axons. Increased focus on studying lipid messengers found in neurons such as endocannabinoids (eCBs) has importance due to their potential axonal pathway regenerative properties. 2-Arachidonoylglycerol (2-AG), a common eCB, is synthesized from an sn-1 hydrolysis reaction between diacylglycerol (DAG) and diacylglycerol lipase (DAGL). Examination of DAG production allows for future downstream analysis in relation to DAGL functionality. Here, we describe protocol guidelines for extracting RGCs from mouse retinas and subsequent mass spectrometry analysis of the DAG content present within the RGCs.

Design and Simulation of a Hierarchical Parallel Distributed Processing Model for Orientation Selection Based on Primary Visual Cortex.

The study of the human visual system not only helps to understand the mechanism of the visual system but also helps to develop visual aid systems to help the visually impaired. As the systematic study of neural signal processing mechanisms in early biological vision continues, the hierarchical structure of the visual system is gradually being dissected, bringing the possibility of building brain-like computational models from a bionic perspective. In this paper, we follow the objective facts of neurobiology and propose a parallel distributed processing computational model of primary visual cortex orientation selection with reference to the complex process of visual signal processing and transmission between the retina to the primary visual cortex, the hierarchical receptive field structure between cells in each layer, and the very fine-grained parallel distributed characteristics of cortical visual computation, which allow for high speed and efficiency. We approach the design from a brain-like chip perspective, map our network model on the field programmable gate array (FPGA), and perform simulation experiments. The results verify the possibility of implementing our proposed model with programmable devices, which can be applied to small wearable devices with low power consumption and low latency.

Insufficient Oligodendrocyte Turnover in Optic Nerve Contributes to Age-Related Axon Loss and Visual Deficits.

Age-related decline in visual functions is a prevalent health problem among elderly people, and no effective therapies are available up-to-date. Axon degeneration and myelin loss in optic nerves (ONs) are age-dependent and become evident in middle-aged (13-18 months) and old (20-22 months) mice of either sex compared with adult mice (3-8 months), accompanied by functional deficits. Oligodendrocyte (OL) turnover is actively going on in adult ONs. However, the longitudinal change and functional significance of OL turnover in aging ONs remain largely unknown. Here, using cell-lineage labeling and tracing, we reported that oligodendrogenesis displayed an age-dependent decrease in aging ONs. To understand whether active OL turnover is required for maintaining axons and visual function, we conditionally deleted the transcription factor Olig2 in the oligodendrocyte precursor cells of young mice. Genetically dampening OL turnover by Olig2 ablation resulted in accelerated axon loss and retinal degeneration, and subsequently impaired ON signal transmission, suggesting that OL turnover is an important mechanism to sustain axon survival and visual function. To test whether enhancing oligodendrogenesis can prevent age-related visual deficits, 12-month-old mice were treated with clemastine, a pro-myelination drug, or induced deletion of the muscarinic receptor 1 in oligodendrocyte precursor cells. The clemastine treatment or muscarinic receptor 1 deletion significantly increased new OL generation in the aged ONs and consequently preserved visual function and retinal integrity. Together, our data indicate that dynamic OL turnover in ONs is required for axon survival and visual function, and enhancing new OL generation represents a potential approach to reversing age-related declines of visual function.SIGNIFICANCE STATEMENT Oligodendrocyte (OL) turnover has been reported in adult optic nerves (ONs), but the longitudinal change and functional significance of OL turnover during aging remain largely unknown. Using cell-lineage tracing and oligodendroglia-specific manipulation, this study reported that OL generation was active in adult ONs and the efficiency decreased in an age-dependent manner. Genetically dampening OL generation by Olig2 ablation resulted in significant axon loss and retinal degeneration, along with delayed visual signal transmission. Conversely, pro-myelination approaches significantly increased new myelin generation in aging ONs, and consequently preserved retinal integrity and visual function. Our findings indicate that promoting OL generation might be a promising strategy to preserve visual function from age-related decline.

Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations.

Introduction: Color vision defects (CVDs) are conditions characterized by the alteration of normal trichromatic vision. CVDs can arise as the result of alterations in three genes (OPN1LW, OPN1MW, OPN1SW) or as a combination of genetic predisposition and environmental factors. To date, apart from Mendelian CVDs forms, nothing is known about multifactorial CVDs forms. Materials and Methods: Five hundred and twenty individuals from Silk Road isolated communities were genotyped and phenotypically characterized for CVDs using the Farnsworth D-15 color test. The CVDs traits Deutan-Protan (DP) and Tritan (TR) were analysed. Genome Wide Association Study for both traits was performed, and results were corrected with a False Discovery Rate linkage-based approach (FDR-p). Gene expression of final candidates was investigated using a published human eye dataset, and pathway analysis was performed. Results: Concerning DP, three genes: PIWIL4 (FDR-p: 9.01*10-9), MBD2 (FDR-p: 4.97*10-8) and NTN1 (FDR-p: 4.98*10-8), stood out as promising candidates. PIWIL4 is involved in the preservation of Retinal Pigmented Epithelium (RPE) homeostasis while MBD2 and NTN1 are both involved in visual signal transmission. With regards to TR, four genes: VPS54 (FDR-p: 4.09*10-9), IQGAP (FDR-p: 6,52*10-10), NMB (FDR-p: 8.34*10-11), and MC5R (FDR-p: 2.10*10-8), were considered promising candidates. VPS54 is reported to be associated with Retinitis pigmentosa; IQGAP1 is reported to regulate choroidal vascularization in Age-Related Macular Degeneration; NMB is involved in RPE homeostasis regulation; MC5R is reported to regulate lacrimal gland function. Discussion: Overall, these results provide novel insights regarding a complex phenotype (i.e., CVDs) in an underrepresented population such as Silk Road isolated communities.

Astrocyte derived TSP2 contributes to synaptic alteration and visual dysfunction in retinal ischemia/reperfusion injury

BackgroundDespite current intervention measures/therapies are able to ameliorate neuronal death following retinal injuries/diseases, the recovery of visual function remains unsatisfactory. Previous studies revealed that the retinal synapse and neurite changed during the early stage after retinopathy, which was considered to be detrimental to visual signal transmission. However, the specific profiles and the mechanisms underlying retinal neurite and synaptic alteration after retinal pathologies remain poorly understood.MethodsHere, we revealed the spatiotemporal pattern of neurite and synaptic alteration following retinal pathologies using a rat model of acute RI/R induced by high intraocular pressure (HIOP) with Western blotting, Immunofluorescence, and electron microscopy. We further explored the potential role of activated astrocytes and their derived thrombospondin 2 (TSP2) in RI/R induced retinal neurite and synaptic alteration and visual dysfunction through viral transduction and drug injection.ResultsWe found a defasciculation of RGC axons, a compensatory increase of presynaptic proteins (synaptophysin and synapsin 1) and synaptic vesicles between bipolar cells and ganglion cells in the inner plexiform layer (IPL), and the degenerated visual function preceded the neuronal death in rat retinae. These events were accompanied by the activation of astrocytes. Furthermore, we showed that suppressing the activation of astrocytes (intravitreal injection of fluorocitric acid, FC), TSP2 knockdown (TSP2 shRNA-AAV transduction), and competitively inhibiting the binding of TSP2 and α2δ1 (intraperitoneal injection of gabapentin, GBP) effectively alleviated the retinal synaptic and neurite alteration and the visual dysfunction following RI/R injury.Conclusions(1) At the early stage following RI/R injury, the rat retinae develop a degeneration of ganglion cell axons and the resulting compensatory synaptic remodeling between bipolar cells and ganglion cells in IPL. These changes occur earlier than the massive loss of neurons in the ganglion cell layer (GCL). (2) Activated astrocytes may secret TSP2, which bind to α2δ1, to mediate the degeneration of rat retinal ganglion cell axons, compensatory synaptic remodeling in IPL, and visual dysfunction following RI/R injury.

A Timestamp-Independent Haptic–Visual Synchronization Method for Haptic-Based Interaction System

The booming haptic data significantly improve the users’ immersion during multimedia interaction. As a result, the study of a Haptic-based Interaction System has attracted the attention of the multimedia community. To construct such a system, a challenging task is the synchronization of multiple sensorial signals that is critical to the user experience. Despite audio-visual synchronization efforts, there is still a lack of a haptic-aware multimedia synchronization model. In this work, we propose a timestamp-independent synchronization for haptic–visual signal transmission. First, we exploit the sequential correlations during delivery and playback of a haptic–visual communication system. Second, we develop a key sample extraction of haptic signals based on the force feedback characteristics and a key frame extraction of visual signals based on deep-object detection. Third, we combine the key samples and frames to synchronize the corresponding haptic–visual signals. Without timestamps in the signal flow, the proposed method is still effective and more robust in complicated network conditions. Subjective evaluation also shows a significant improvement of user experience with the proposed method.

Glutamate Transporters EAAT2 and EAAT5 Differentially Shape Synaptic Transmission from Rod Bipolar Cell Terminals.

Excitatory amino acid transporters (EAATs) control visual signal transmission in the retina by rapidly removing glutamate released from photoreceptors and bipolar cells (BCs). Although it has been reported that EAAT2 and EAAT5 are expressed at presynaptic terminals of photoreceptors and some BCs in mammals, the distinct functions of these two glutamate transporters in retinal synaptic transmission, especially at a single synapse, remain elusive. In this study, we found that EAAT2 was expressed in all BC types while coexisting with EAAT5 in rod bipolar (RB) cells and several types of cone BCs from mice of either sex. Our immunohistochemical study, together with a recently published literature (Gehlen et al., 2021), showed that EAAT2 and EAAT5 were both located in RB axon terminals near release sites. Optogenetic, electrophysiological and pharmacological analyses, however, demonstrated that EAAT2 and EAAT5 regulated neurotransmission at RB→AII amacrine cell synapses in significantly different ways: EAAT5 dramatically affected both the peak amplitude and kinetics of postsynaptic responses in AIIs, whereas EAAT2 had either relatively small or opposite effects. By contrast, blockade of EAAT1/GLAST, which was exclusively expressed in Müller cells, showed no obvious effect on AII responses, indicating that glutamate uptake by Müller cells did not influence synaptic transmission from RB terminals. Furthermore, we found that temporal resolution at RB→AII synapses was reduced substantially by blockade of EAAT5 but not EAAT2. Taken together, our work reveals the distinct functions of EAAT2 and EAAT5 in signal transmission at RB ribbon synapses.

AI-Enabled Cross-Modal Communications

When haptic signals are integrated with existing audio-visual dominated multimedia applications, multi-modal services that can satisfy an individual's immersive experience have emerged. In order to support multi-modal services, cross-modal communications come into being. However, facing collaborative transmission and comprehensive processing requirements of audio, visual, and haptic signals as well as their influences for user's immersive experience, the research of cross-modal communications is still in its infancy and needs to tackle many technical challenges. Due to great successes and powerful abilities of artificial intelligence (AI), it can be expected to underpin cross-modal communications. In this article, we try to deal with issues in cross-modal communications by using AI technology. Specifically, we first adopt the federated learning paradigm to solve sparse data collection and privacy protection problems in the immersive experience description of multi-modal services. Then, we resort to the reinforcement learning paradigm to construct a joint optimization framework of caching, communication, and computation, realizing collaborative transmission of audio, visual, and haptic streams. Finally, we attempt to use the transfer learning paradigm to extract, transfer, and fuse knowledge, semantics, and characteristics from different modalities, recovering corrupted signals and promoting rendering effects at the receiver. Experimental results validate the effectiveness of the AI-enabled cross-modal communications strategies.

M1-Type, but Not M4-Type, Melanopsin Ganglion Cells Are Physiologically Tuned to the Central Circadian Clock.

Proper circadian photoentrainment is crucial for the survival of many organisms. In mammals, intrinsically photosensitive retinal ganglion cells (ipRGCs) can use the photopigment melanopsin to sense light independently from rod and cone photoreceptors and send this information to many brain nuclei such as the suprachiasmatic nucleus (SCN), the site of the central circadian pacemaker. Here, we measure ionic currents and develop mathematical models of the electrical activity of two types of ipRGCs: M1, which projects to the SCN, and M4, which does not. We illustrate how their ionic properties differ, mainly how ionic currents generate lower spike rates and depolarization block in M1 ipRGCs. Both M1 and M4 cells have large geometries and project to higher visual centers of the brain via the optic nerve. Using a partial differential equation model, we show how axons of M1 and M4 cells faithfully convey information from the soma to the synapse even when the signal at the soma is attenuated due to depolarization block. Finally, we consider an ionic model of circadian photoentrainment from ipRGCs synapsing on SCN neurons and show how the properties of M1 ipRGCs are tuned to create accurate transmission of visual signals from the retina to the central pacemaker, whereas M4 ipRGCs would not evoke nearly as efficient a postsynaptic response. This work shows how ipRGCs and SCN neurons' electrical activities are tuned to allow for accurate circadian photoentrainment.

Evidence for aposematism in a southern hemisphere stonefly family (Plecoptera: Austroperlidae)

AbstractAposematism is a phenomenon in which defended prey advertise their unprofitability to predators through conspicuous signals. Aposematic (warning) colouration is widespread across numerous insect orders but rarely occurs in insects that inhabit aquatic environments where conditions can impose constraints on visual signal transmission. In the semi‐aquatic insect order Plecoptera (stoneflies), only the terrestrial adult stage of Austroperla cyrene (Austroperlidae) from New Zealand has been suggested to possess aposematic colouration, associated with the presence of hydrogen cyanide and documented unpalatability to predators. Here, we review evidence for the occurrence of aposematic colouration in Australian and South American Austroperlidae based on a synthesis of taxonomic literature and studies examining feeding preferences of predators in aquatic environments. Contrasting black, white and yellow colouration occurs commonly in adult Austroperlidae, and nymphs of several surveyed species were found to be aversive to predators, together suggesting that aposematism may be widespread in this family. The wider prevalence of aposematism in Austroperlidae should be examined further by directly testing the palatability of various species to predators and by analysing the chemical compositions of their defensive secretions. Austroperlid stoneflies offer new potential for understanding the evolution of aposematism in ecological and phylogenetic contexts that have not yet been explored.

Human mesenchymal stem cell therapy promotes retinal ganglion cell survival and target reconnection after optic nerve crush in adult rats

BackgroundOptic-nerve injury results in impaired transmission of visual signals to central targets and leads to the death of retinal ganglion cells (RGCs) and irreversible vision loss. Therapies with mesenchymal stem cells (MSCs) from different sources have been used experimentally to increase survival and regeneration of RGCs.MethodsWe investigated the efficacy of human umbilical Wharton’s jelly-derived MSCs (hWJ-MSCs) and their extracellular vesicles (EVs) in a rat model of optic nerve crush.ResultshWJ-MSCs had a sustained neuroprotective effect on RGCs for 14, 60, and 120 days after optic nerve crush. The same effect was obtained using serum-deprived hWJ-MSCs, whereas transplantation of EVs obtained from those cells was ineffective. Treatment with hWJ-MSCs also promoted axonal regeneration along the optic nerve and reinnervation of visual targets 120 days after crush.ConclusionsThe observations showed that this treatment with human-derived MSCs promoted sustained neuroprotection and regeneration of RGCs after optic nerve injury. These findings highlight the possibility to use cell therapy to preserve neurons and to promote axon regeneration, using a reliable source of human MSCs.

Temporal recalibration in vision requires location-based binding

Occupying the same location and occurring at the same time are the essential spatial and temporal factors for different features of a natural event or object to be integrated. Audio-visual temporal recalibration, as a temporal integration mechanism, refers to the brain's capacity to perceive simultaneity by adjusting for differential delays in the transmission of auditory and visual signals. Co-localization of auditory and visual information, however, is found not to be necessary for audio-visual temporal recalibration to occur. Here, we show that after exposure to a time lag between a visual flash and a visual collision, simultaneity responses were shifted toward an adapt lag in a bound condition where the flash and collision belonged to the same object but not in a separate condition where the flash and collision belonged to spatially separated objects. The results demonstrate that location-based binding is a requisite for temporal recalibration within the visual modality. Our finding suggests that the brain takes the modality difference in object localization into consideration when integrating temporally asynchronous signals.

Dopaminergic Retinal Cell Loss and Visual Dysfunction in Parkinson Disease.

Considering the demonstrated implication of the retina in Parkinson disease (PD) pathology and the importance of dopaminergic cells in this tissue, we aimed to analyze the state of the dopaminergic amacrine cells and some of their main postsynaptic neurons in the retina of PD. Using immunohistochemistry and confocal microscopy, we evaluated morphology, number, and synaptic connections of dopaminergic cells and their postsynaptic cells, AII amacrine and melanopsin-containing retinal ganglion cells, in control and PD eyes from human donors. In PD, dopaminergic amacrine cell number was reduced between 58% and 26% in different retinal regions, involving a decline in the number of synaptic contacts with AII amacrine cells (by 60%) and melanopsin cells (by 35%). Despite losing their main synaptic input, AII cells were not reduced in number, but they showed cellular alterations compromising their adequate function: (1) a loss of mitochondria inside their lobular appendages, which may indicate an energetic failure; and (2) a loss of connexin 36, suggesting alterations in the AII coupling and in visual signal transmission from the rod pathway. The dopaminergic system impairment and the affection of the rod pathway through the AII cells may explain and be partially responsible for the reduced contrast sensitivity or electroretinographic response described in PD. Also, dopamine reduction and the loss of synaptic contacts with melanopsin cells may contribute to the melanopsin retinal ganglion cell loss previously described and to the disturbances in circadian rhythm and sleep reported in PD patients. These data support the idea that the retina reproduces brain neurodegeneration and is highly involved in PD pathology. ANN NEUROL 2020;88:893-906.

Evaluation and comparison of global-feature-based and local-feature-based segmentation algorithms in intracranial visual pathway delineation.

Intracranial visual pathway is related to the effective transmission of visual signals to brain. It was not only the target organ of diseases but also the organs at risk in radiotherapy thus its delineation plays an important role in both diagnosis and treatment planning. Traditional manual segmentation method suffered from time- and labor- consuming as well as intra- and inter- variability. In order to overcome these problems, state-of-the-art segmentation models were designed and various features were extracted and utilized, but it's hard to tell their effectiveness on intracranial visual pathway delineation. It's because that these methods worked on different dataset and accompanied with different training tricks. This study aimed to research the contribution of global features and local features in delineating the intracranial visual pathway from MRI scans. The two typical segmentation models, 3D UNet and DeepMedic, were chosen since they focused on global features and local features respectively. We constructed the hybrid model through serially connecting the two mentioned models to validate the performance of combined global and local features. Validation results showed that the hybrid model outperformed the individual ones. It proved that multi scale feature fusion was important in improving the segmentation performance.

Suppression of Gq and PLC gene expression has a small effect on quantum bumps in vivo in Periplaneta americana

Visual signal transmission by Drosophila melanogaster photoreceptors is mediated by a Gq protein that activates a phospholipase C (PLC). Mutations and deficiencies in expression of either of these proteins cause severe defects in phototransduction. Here we investigated whether these proteins are also involved in the cockroach, Periplaneta americana, phototransduction by silencing Gq α-subunit (Gqα) and phosphoinositide-specific phospholipase C (PLC) by RNA interference and observing responses to single photons (quantum bumps, QB). We found (1) non-specific decreases in membrane resistance, membrane capacitance and absolute sensitivity in the photoreceptors of both Gqα and PLC knockdowns, and (2) small changes in QB statistics. Despite significant decreases in expressions of Gq and PLC mRNA, the changes in QB properties were surprisingly modest, with mean latencies increasing by ~ 10%, and without significant decrease in their amplitudes. To better understand our results, we used a mathematical model of the phototransduction cascade. By modifying the Gq and PLC abundances, and diffusion rates for Gq, we found that QB latencies and amplitudes deteriorated noticeably only after large decreases in the protein levels, especially when Gq diffusion was slow. Also, reduction in Gq but not PLC lowered quantum efficiency. These results suggest that expression of the proteins may be redundant.