Corticothalamic feedback sculpts visual spatial integration in mouse thalamus.

En route from the retina to the cortex, visual information passes through the dorsolateral geniculate nucleus (dLGN) of the thalamus, where extensive corticothalamic (CT) feedback has been suggested to modulate spatial processing. How this modulation arises from direct excitatory and indirect inhibitory CT feedback pathways remains enigmatic. Here, we show that in awake mice, retinotopically organized cortical feedback sharpens receptive fields (RFs) and increases surround suppression in the dLGN. Guided by a network model indicating that widespread inhibitory CT feedback is necessary to reproduce these effects, we targeted the visual sector of the thalamic reticular nucleus (visTRN) for recordings. We found that visTRN neurons have large RFs, show little surround suppression and exhibit strong feedback-dependent responses to large stimuli. These features make them an ideal candidate for mediating feedback-enhanced surround suppression in the dLGN. We conclude that cortical feedback sculpts spatial integration in the dLGN, likely via recruitment of neurons in the visTRN.

Effects of locomotion extend throughout the mouse early visual system.

BACKGROUND: Neural responses in visual cortex depend not only on sensory input but also on behavioral context. One such context is locomotion, which modulates single-neuron activity in primary visual cortex (V1). How locomotion affects neuronal populations across cortical layers and in precortical structures is not well understood. RESULTS: We performed extracellular multielectrode recordings in the visual system of mice during locomotion and stationary periods. We found that locomotion influenced activity of V1 neurons with a characteristic laminar profile and shaped the population response by reducing pairwise correlations. Although the reduction of pairwise correlations was restricted to cortex, locomotion slightly but consistently increased firing rates and controlled tuning selectivity already in the dorsolateral geniculate nucleus (dLGN) of the thalamus. At the level of the eye, increases in locomotion speed were associated with pupil dilation. CONCLUSIONS: These findings document further, nonmultiplicative effects of locomotion, reaching earlier processing stages than cortex.

Spatial integration in mouse primary visual cortex.

Responses of many neurons in primary visual cortex (V1) are suppressed by stimuli exceeding the classical receptive field (RF), an important property that might underlie the computation of visual saliency. Traditionally, it has proven difficult to disentangle the underlying neural circuits, including feedforward, horizontal intracortical, and feedback connectivity. Since circuit-level analysis is particularly feasible in the mouse, we asked whether neural signatures of spatial integration in mouse V1 are similar to those of higher-order mammals and investigated the role of parvalbumin-expressing (PV+) inhibitory interneurons. Analogous to what is known from primates and carnivores, we demonstrate that, in awake mice, surround suppression is present in the majority of V1 neurons and is strongest in superficial cortical layers. Anesthesia with isoflurane-urethane, however, profoundly affects spatial integration: it reduces the laminar dependency, decreases overall suppression strength, and alters the temporal dynamics of responses. We show that these effects of brain state can be parsimoniously explained by assuming that anesthesia affects contrast normalization. Hence, the full impact of suppressive influences in mouse V1 cannot be studied under anesthesia with isoflurane-urethane. To assess the neural circuits of spatial integration, we targeted PV+ interneurons using optogenetics. Optogenetic depolarization of PV+ interneurons was associated with increased RF size and decreased suppression in the recorded population, similar to effects of lowering stimulus contrast, suggesting that PV+ interneurons contribute to spatial integration by affecting overall stimulus drive. We conclude that the mouse is a promising model for circuit-level mechanisms of spatial integration, which relies on the combined activity of different types of inhibitory interneurons.

Corneal stromal ablation with femtosecond ultraviolet pulses in rabbits.

PURPOSE: To determine the effectiveness of femtosecond ultraviolet (UV) pulses in ablating corneal stroma in a rabbit model and to compare the healing response between eyes treated with femtosecond UV pulses and eyes treated with standard excimer photorefractive keratectomy. SETTING: Laser Research Center, Vilnius University, Vilnius, Lithuania. DESIGN: Experimental study. METHODS: Myopic photoablation using a femtosecond UV solid-state laser system was applied to corneas of pigmented rabbits. Experiments in 16 eyes were performed for optimization of the laser system parameters (fluence, spot size, pulse repetition rate) and calibration of ablation rate. In 7 rabbits, deep femtosecond UV ablation (∼130 µm) in 1 eye and shallow ablation (∼30 µm) in the contralateral eye were performed. Nine rabbits received an approximately 30 µm ablation with femtosecond UV pulses in 1 eye and with a conventional excimer system in the contralateral eye. Two eyes were used as controls. The ablation process and surface-temperature dynamics were monitored and recorded. Surface quality and haze development were evaluated. Rabbits were humanely killed 0 to 6 months after surgery, and eyes were enucleated for histological examination. RESULTS: Rabbit corneas ablated with femtosecond UV pulses or excimer laser radiation were similar in terms of the corneal wound-healing process, surface quality, and histology. CONCLUSIONS: The experiments indicate the feasibility of clinical application of femtosecond UV lasers for stromal ablation. The ability to switch between laser harmonics allows fast changeover from infrared to the UV mode, implying that a wide range of ophthalmic procedures can be performed using a single solid-state laser device. FINANCIAL DISCLOSURE: Ms. Gabryte and Mr. Danielius are paid employees of Light Conversion Ltd. Mr. Danielius is a shareholder of Light Conversion Ltd. No other author has a financial or proprietary interest in any material or method mentioned.

Corneal shaping and ablation of transparent media by femtosecond pulses in deep ultraviolet range.

PURPOSE: To assess the performance of a newly developed solid-state femtosecond ultraviolet (UV) laser system in corneal ablation. SETTING: Vilnius University, Laser Research Centre, Vilnius, Lithuania. METHODS: Femtosecond pulses in the deep UV range (205 nm) were obtained by the generation of the fifth-harmonic of an amplified Yb:KGW laser system (fundamental output at 1027 nm). Coupled with galvanometric beam-scanning mirrors, this system allowed ablation shaping of transparent media, including poly(methyl methacrylate) (PMMA), collagen, and ex vivo porcine corneas. The surfaces of ablated structures were characterized using a noncontact confocal optical profiler. RESULTS: Spherical structures were successfully formed in all 3 materials tested. A 10.0 diopter refraction change in the cornea was produced in 180 seconds. The resulting surface quality was significantly higher (roughness length >100 microm versus approximately 6 microm) in gelatin and ex vivo corneas than in PMMA. CONCLUSION: The solid-state femtosecond UV laser system seems an attractive alternative to the currently used ophthalmic argon-fluoride excimer laser system because of its small footprint, silent operation, and ability to generate femtosecond light pulses at both 1027 nm (suitable for flap creation) and 205 nm (corneal ablation).