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At least 685 records · Page 38Linked to original sources
PubMed1993

Experience-dependent plasticity in the inferior colliculus: a site for visual calibration of the neural representation of auditory space in the barn owl.

The optic tectum (homolog of the superior colliculus) contains mutually aligned neural maps of auditory and visual space. During development, the organization of the auditory map is guided by spatial information provided by vision: barn owls raised wearing prismatic spectacles, which optically shift the visual field and the visual map in the optic tectum, develop an auditory map that is shifted by an approximately equivalent amount, such that alignment between the two maps is preserved (Knudsen and Brainard, 1991). In this study we investigated whether this shift in the auditory map is intrinsic to the optic tectum or whether it reflects plasticity at an earlier stage in the auditory pathway. Owls were raised wearing prismatic spectacles that displaced the visual field by 23 degrees to the left or right. This manipulation alters the normal correspondence between locations in the visual field and interaural time difference (ITD), the primary cue for the azimuth of a sound source. In normal owls and in owls with at least 150 d of prism experience, extracellular unit recordings were used to assess the representations of ITD at anatomically and physiologically defined sites in the optic tectum and in the two prior stages of the auditory pathway, the external and central nuclei of the inferior colliculus (ICx and ICc). In the optic tectum of normal owls, the values of ITD to which units responded most strongly (best ITDs) varied systematically with the azimuths of unit visual receptive fields (VRFs). In the prism-reared owls, best ITDs were shifted from normal toward the values of ITD produced by sounds at the locations of the units' optically displaced VRFs. In the ICx of prism-reared owls, the representation of ITD also was shifted from normal, by an amount and in a direction that could completely account for the shift in ITD measured in the optic tectum. At some sites in the ICx, the shift in ITD tuning was apparent within the first 7-8 msec of the response; shifted tuning at such short latencies argues that the altered representation of ITD in the ICx reflects plasticity in the ascending auditory pathway, and is not the result of descending activity from higher auditory centers. In the ICc, which immediately precedes the ICx in the ascending pathway, the representation of ITD was normal. The results indicate that the visual instruction of auditory spatial tuning of neurons in the optic tectum reflects plasticity at the level of the ICx, the site where the auditory map of space is first synthesized.

Acoustic Stimulation↗
PubMed1997

MAP 0, a 400-kDa microtubule-associated protein unique to teleost fish.

Microtubules from neural tissues of the Atlantic cod, Gadus morhua, and of several species of Antarctic teleosts are composed of tubulin and several microtubule-associated proteins (MAPs), one of which has an apparent molecular weight of approximately 400-430 kDa. Because its apparent molecular weight exceeds those of the MAP 1 proteins, we designate this high molecular weight teleost protein MAP 0. Cod MAP 0 failed to cross-react with antibodies specific for MAPs 1A, 1B and 2 of mammalian brain, for MAP H1 of squid optic lobe, and for chicken erythrocyte syncolin, which suggests that it has a novel structure. Similarly, MAP 0 from the Antarctic fish was not recognized by an antibody specific for bovine MAP 2. Together, these observations suggest that MAP 0 is a novel MAP that may be unique to fish. To determine the tissue specificity and phylogenetic distribution of this protein, we generated a rabbit polyclonal antibody against cod MAP 0. Using this antibody, we found that MAP 0 was present in microtubule proteins isolated from cod brain tissues and spinal cord but was absent in microtubules from heart, liver, and spleen. At the subcellular level, MAP 0 was distributed in cod brain cells in a punctate pattern coincident with microtubules but was absent in skin cells. MAP 0 was also detected in cells of the peripheral nervous system. A survey of microtubule proteins from chordates and invertebrates showed that anti-MAP 0-reactive homologs were present in five teleost species but not in more primitive fish and invertebrates or in higher vertebrates. MAP 0 bound to cod microtubules by ionic interaction at a site recognized competitively by bovine MAP 2. Although its function is unknown, MAP 0 does not share the microtubule-binding properties of the motor proteins kinesin and dynein. We propose that MAP 0 is a unique, teleost-specific MAP.

Amphibians↗
PubMed1999

Mapping the sensitivity of T cells with an optical trap: polarity and minimal number of receptors for Ca(2+) signaling.

Contact with antigen-presenting cells (APCs) initiates an activation cascade within T lymphocytes, including a rise in cytosolic calcium, lymphokine production, and cell division. Although T cell-APC physical contact is required for an immune response, little is known about the patterns of cellular interactions and their relation to activation. Calcium imaging combined with an optical trap enabled the T cell contact requirements and polarity to be investigated at the single-cell level. APCs or anti-CD3 mAb-coated beads were trapped with a laser and placed at different locations along the T cell, which has a polarized appearance defined by the shape and direction of crawling. T cells were 3-fold more sensitive to APC contact made at the leading edge of the T cell than with contact made at the tail. Anti-CD3 mAb-coated 6-micrometer beads induced calcium signaling with approximately 10-fold higher frequency and approximately 4-fold shorter latency on contact with the leading edge of the T cell than on contact with the trailing edge. Alterations in antibody density (2 to 500 per micrometer(2)) and bead size (1 to 6 micrometer in diameter) were used to determine the spatial requirements and the minimal number of receptors which must be engaged to transmit a positive signal. T cell response percentage, latency, and calcium-signaling pattern (transient vs. sustained or oscillatory) depended on antibody density on the bead. The presence of approximately 170 anti-CD3 mAb within the contact area elicited a detectable T cell calcium response. We propose here that engagement of no more than 340 T cell receptors (approximately 1% of the total on the cell) is sufficient to initiate Ca(2+) signaling. The minimal contact area was approximately 3 micrometer(2).

Animals↗
PubMed2003

Functional near-infrared optical imaging: utility and limitations in human brain mapping.

Although near-infrared spectroscopy (NIRS) was developed as a tool for clinical monitoring of tissue oxygenation, it also has potential for neuroimaging. A wide range of different NIRS instruments have been developed, and instruments for continuous intensity measurements with fixed spacing [continuous wave (CW)-type instruments], which are most readily available commercially, allow us to see dynamic changes in regional cerebral blood flow in real time. However, quantification, which is necessary for imaging of brain functions, is impossible with these CW-type instruments. Over the past 20 years, many different approaches to quantification have been tried, and several multichannel time-resolved and frequency-domain instruments are now in common use for imaging. Although there are still many problems with this technique, such as incomplete knowledge of how light propagates through the head, NIRS will not only open a window on brain physiology for subjects who have rarely been examined until now, but also provide a new direction for functional mapping studies.

Algorithms↗
PubMed2004

Performance of a commercial optical CT scanner and polymer gel dosimeters for 3-D dose verification.

Performance analysis of a commercial three-dimensional (3-D) dose mapping system based on optical CT scanning of polymer gels is presented. The system consists of BANG 3 polymer gels (MGS Research, Inc., Madison, CT), OCTOPUS laser CT scanner (MGS Research, Inc., Madison, CT), and an in-house developed software for optical CT image reconstruction and 3-D dose distribution comparison between the gel, film measurements and the radiation therapy treatment plans. Various sources of image noise (digitization, electronic, optical, and mechanical) generated by the scanner as well as optical uniformity of the polymer gel are analyzed. The performance of the scanner is further evaluated in terms of the reproducibility of the data acquisition process, the uncertainties at different levels of reconstructed optical density per unit length and the effects of scanning parameters. It is demonstrated that for BANG 3 gel phantoms held in cylindrical plastic containers, the relative dose distribution can be reproduced by the scanner with an overall uncertainty of about 3% within approximately 75% of the radius of the container. In regions located closer to the container wall, however, the scanner generates erroneous optical density values that arise from the reflection and refraction of the laser rays at the interface between the gel and the container. The analysis of the accuracy of the polymer gel dosimeter is exemplified by the comparison of the gel/OCT-derived dose distributions with those from film measurements and a commercial treatment planning system (Cadplan, Varian Corporation, Palo Alto, CA) for a 6 cm x 6 cm single field of 6 MV x rays and a 3-D conformal radiotherapy (3DCRT) plan. The gel measurements agree with the treatment plans and the film measurements within the "3%-or-2 mm" criterion throughout the usable, artifact-free central region of the gel volume. Discrepancies among the three data sets are analyzed.

Equipment Design↗
PubMed2003

Selective loss of orientation column maps in visual cortex during brief elevation of intraocular pressure.

PURPOSE: To compare the orientation column maps elicited by different spatial frequency gratings in cortical area 17 of cats before and during brief elevation of intraocular pressure (IOP). METHODS: IOP was elevated by injecting saline into the anterior chamber of a cat's eye through a syringe needle. The IOP was elevated enough to cause a retinal perfusion pressure (arterial pressure minus IOP) of approximately 30 mm Hg during a brief elevation of IOP. The visual stimulus gratings were varied in spatial frequency, whereas other parameters were kept constant. The orientation column maps of the cortical area 17 were monocularly elicited by drifting gratings of different spatial frequencies and revealed by a brain intrinsic signal optical imaging system. These maps were compared before and during short-term elevation of IOP. RESULTS: The response amplitude of the orientation maps in area 17 decreased during a brief elevation of IOP. This decrease was dependent on the retinal perfusion pressure but not on the absolute IOP. The location of the most visible maps was spatial-frequency dependent. The blurring or loss of the pattern of the orientation maps was most severe when high-spatial-frequency gratings were used and appeared most significantly on the posterior part of the exposed cortex while IOP was elevated. However, the basic patterns of the maps remained unchanged. Changes in cortical signal were not due to changes in the optics of the eye with elevation of IOP. CONCLUSIONS: A stable normal IOP is essential for maintaining normal visual cortical functions. During a brief and high elevation of IOP, the cortical processing of high-spatial-frequency visual information was diminished because of a selectively functional decline of the retinogeniculocortical X pathway by a mechanism of retinal circulation origin.

Animals↗
PubMed1983

Some topological considerations of the optic pathway.

The contralateral projection of the vertebrate retinotopic map has a component of a mirror or uniaxial inversion in it. Here, a simple hypothesis is proposed which explains how this can come about. The emphasis is on topological considerations, in a global sense, of the overall map. An important feature of the hypothesis is that the optic nerve fibres follow pathways such that they retain their nearest neighbour relationships till they terminate in the optic tectum, i.e. no criss-crossing of the fibres is envisaged. Anatomical evidence for this is already available in the case of the optic tract of frog. Some speculations are also suggested concerning the role of this uniaxial inversion in information processing. The observations of optic tracts of other amphibian and some lower vertebrate systems are also considered.

Animals↗
PubMed2005

From flow to map in an experimental high-dimensional electro-optic nonlinear delay oscillator.

An optoelectronic nonlinear delay oscillator seeded by a pulsed laser source is used to experimentally demonstrate a new transition scenario for the general class of delay differential dynamics, from continuous to discrete time behavior. This transition scenario differs from the singular limit map, or adiabatic approximation model that is usually considered. The transition from the map to the flow is observed when increasing the pulse repetition rate. The mechanism of this transition opens the way to new interpretations of the general properties of delay differential dynamics, which are universal features of many other scientific domains. We anticipate that the nonlinear delay oscillator architecture presented here will have significant applications in chaotic communication systems.

Journal Article↗
PubMed1997

Membrane specific mapping and colocalization of malarial and host skeletal proteins in the Plasmodium falciparum infected erythrocyte by dual-color near-field scanning optical microscopy.

Accurate localization of proteins within the substructure of cells and cellular organelles enables better understanding of structure-function relationships, including elucidation of protein-protein interactions. We describe the use of a near-field scanning optical microscope (NSOM) to simultaneously map and detect colocalized proteins within a cell, with superresolution. The system we elected to study was that of human red blood cells invaded by the human malaria parasite Plasmodium falciparum. During intraerythrocytic growth, the parasite expresses proteins that are transported to the erythrocyte cell membrane. Association of parasite proteins with host skeletal proteins leads to modification of the erythrocyte membrane. We report on colocalization studies of parasite proteins with an erythrocyte skeletal protein. Host and parasite proteins were selectively labeled in indirect immunofluorescence antibody assays. Simultaneous dual-color excitation and detection with NSOM provided fluorescence maps together with topography of the cell membrane with subwavelength (100 nm) resolution. Colocalization studies with laser scanning confocal microscopy provided lower resolution (310 nm) fluorescence maps of cross sections through the cell. Because the two excitation colors shared the exact same near-field aperture, the two fluorescence images were acquired in perfect, pixel-by-pixel registry, free from chromatic aberrations, which contaminate laser scanning confocal microscopy measurements. Colocalization studies of the protein pairs of mature parasite-infected erythrocyte surface antigen (MESA) (parasite)/protein4.1(host) and P. falciparum histidine rich protein (PfHRP1) (parasite)/protein4.1(host) showed good real-space correlation for the MESA/protein4.1 pair, but relatively poor correlation for the PfHRP1/protein4.1 pair. These data imply that NSOM provides high resolution information on in situ interactions between proteins in biological membranes. This method of detecting colocalization of proteins in cellular structures may have general applicability in many areas of current biological research.

Cells, Cultured↗
PubMed2003

The spatial pattern of response magnitude and selectivity for orientation and direction in cat visual cortex.

Optical imaging studies of orientation and direction preference in visual cortex have typically used vector averaging to obtain angle and magnitude maps. This method has shown half-rotation orientation singularities (pinwheels) located within regions of low orientation vector magnitude. Direction preference is generally orthogonal to orientation preference, but often deviates from this, particularly in regions of low direction vector magnitude. Linear regions of rapid change in direction preference terminate in or near orientation singularities. The vector-averaging method is problematic however because it does not clearly disambiguate spatial variation in orientation tuning width from variation in height. It may also wrongly estimate preferred direction in regions where preference is weak. In this paper we analyze optical maps of cat visual cortex by fitting model tuning functions to the responses. This new method reveals features not previously evident. Orientation tuning height and width vary independently across the map: tuning height is always low near singularities, however regions of broad and narrow orientation tuning width can be found in regions of low tuning height, often alternating in a spoke-like fashion around singularities. Orientation and direction preference angles are always closely orthogonal. Reversals in direction preference form lines that originate precisely in orientation singularities.

Animals↗
PubMed2002

The optic tectum controls visually guided adaptive plasticity in the owl's auditory space map.

The midbrain contains an auditory map of space that is shaped by visual experience. When barn owls are raised wearing spectacles that horizontally displace the visual field, the auditory space map in the external nucleus of the inferior colliculus (ICX) shifts according to the optical displacement of the prisms. Topographic visual activity in the optic tectum could serve as the template that instructs the auditory space map. We studied the effects of a restricted, unilateral lesion in the portion of the optic tectum that represents frontal space. Here we show that such a lesion eliminates adaptive adjustments specifically in the portion of the auditory map that represents frontal space on the same side of the brain, while the rest of the map continues to adjust adaptively. Thus, activity in the tectum calibrates the auditory space map in a location-specific manner. Because the site of adaptive changes is the ICX, the results also indicate that the tectum provides a topographic instructive signal that controls adaptive auditory plasticity in the ICX.

Adaptation, Physiological↗
PubMed1998

Topographical and temporal specificity of human intraoperative optical intrinsic signals.

The goal of this study was to determine the topographical and temporal specificity of neuronal and vascular responses using an intraoperative optical technique (iOIS). The face, thumb, index, and middle fingers were stimulated individually to obtain separate maps of cortical activation. Peak optical responses provided unique, non-overlapping cortical brain maps. Non-peak signals were more dispersed and produced overlapping responses from different digits. Peak iOIS responses colocalized with electrocortical stimulation mapping and evoked potentials. Temporally, we observed statistically significant specificity corresponding to sequential cortical activation during early optical signals (500-1750 ms), but later perfusion responses were non-specific. To our knowledge, this is the first report of either topographical specificity in overlapping spatial patterns, and/or temporal specificity in early perfusion profiles. These results therefore may have significant implications for other perfusion dependent functional imaging techniques.

Anesthesia, General↗
PubMed2001

Comparison of neuronal and hemodynamic measures of the brain response to visual stimulation: an optical imaging study.

The noninvasive mapping of hemodynamic brain activity has led to significant advances in neuroimaging. This approach is based in part on the assumption that hemodynamic changes are proportional to (and therefore constitute a linear measure of) neuronal activity. We report a study investigating the quantitative relationship between neuronal and hemodynamic measures. This study exploited the fact that optical imaging methods can simultaneously provide noninvasive measures of neuronal and hemodynamic activity from the same region of the brain. We manipulated visual stimulation frequency and measured responses from the medial occipital area of 8 young adults. The results were consistent with a model postulating a linear relationship between the neuronal activity integrated over time and the amplitude of the hemodynamic response. The hemodynamic response colocalized with the neuronal response. These data support the use of quantitative neuroimaging methods to infer the intensity and localization of neuronal activity in occipital areas.

Adult↗
PubMed1994

Mapping patterns of neuronal activity and seizure propagation by imaging intrinsic optical signals in the isolated whole brain of the guinea-pig.

Image analysis techniques were used to examine changes in the intrinsic optical properties in the isolated brain of the guinea-pig in order to map normal neuronal activity patterns and seizure propagation in the olfactory cortex. Electrical stimulation of the lateral olfactory tract decreased light reflectance in distant cortical areas where fibres of the tract are known to project. These areas included the amygdalar, anterior and posterior piriform, and entorhinal cortices, as well as the olfactory tubercle. Stimulation of the lateral entorhinal cortex decreased reflectance in a more circumscribed area in the lateral and medial entorhinal cortex. By imaging intrinsic signals in real-time, we also demonstrated that seizure activity elicited in the entorhinal cortex/hippocampus preferentially propagated to the posteromedial cortical amygdaloid nucleus. The magnitudes of the intrinsic optical signals were correlated with the amplitudes of field potentials recorded in laminae II or III of the olfactory cortex of the same preparations. These signals had onset times of approximately 3 s during 5 Hz stimulation, consistently recovered and were graded with stimulation frequency. The generation of the intrinsic signals required postsynaptic activation, since attenuating synaptic transmission with kynurenic acid (an excitatory amino acid antagonist) eliminated the signals. The intrinsic signals exhibited maxima at 425-450, 550 and 600 nm, suggesting that they arose from changes in light absorption by cytochromes. Intrinsic signals of relatively constant magnitude were also present at 400, 475-500 and 575 nm, and at wavelengths greater than 600 nm. This suggested that an additional component of the intrinsic signal arose from changes in light scattering, possibly due to cellular swelling.

Animals↗
PubMed1987

Distribution of axons according to diameter in the monkey's optic tract.

The distribution of axonal diameters in the optic tract of Old World monkeys was examined by light and electron microscopy. Axon diameters were measured in samples of 100 axons taken from several locations in a cross section of the tract about 5 mm behind the optic chiasm. Fine-caliber axons (less than 1.75 micron in diameter) were found in all parts of the tract. Dorsally no coarse axons were present. Further ventrally, coarse axons gradually appeared and increased steadily in proportion. The largest optic axons (greater than 2.5 micron) were found in the most ventral parts of the tract, near the pial surface. This pattern of segregation of axons of differing diameters in the optic tract is a rearrangement of the distribution of axon diameters seen in the nerve rather than a continuation of the same pattern. Examination of axon diameters in the optic nerve has shown that there is a preponderance of fine axons centrally, while coarser axons are found in the periphery, near the pial surface; however, histograms from central parts of the nerve contain a greater proportion of coarse axons than the dorsal parts of the optic tract, while histograms from the periphery of the optic nerve contain a conspicuously greater proportion of fine axons than do histograms from the most ventral parts of the tract. This relatively greater segregation of axons according to diameter in the optic tract demonstrates that the distribution of axons in the tract cannot be formed by the simple combination of two hemiretinal maps contained in each optic nerve, as suggested in classic descriptions.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed2002

Hydrophobic optical elements for near-field optical analysis (NOA) in liquid environment--a preliminary study.

Near-field Scanning Optical Microscopy (NSOM) in liquid environment is expected to allow time resolved morphological mappings on cellular surfaces on the nanoscale level. Near-field Optical Analysis (NOA) via NSOM exploits the energy transfer from the tip of an optical element (tip diameter > or = 20nm), oscillating within the range of the characteristic length of the energy transfer ( approximately 10nm) in the near-field of the surface to be analysed. In NOA, a molecular assembly is monitored by visible light with a resolution far below the wavelength of visible light. Actually, NOA is successfully applied in mapping local optical contrasts, for instance in photonic crystals with dielectric periodicities on the nanoscale. NSOM could in principle be performed in two different modes: tapping mode, with tip-oscillations perpendicular, or shear force mode, with tip-oscillations parallel to the substrate. Both basic modes have specific advantages and disadvantages. In biological systems (e.g. in cell cultures), where scanning in liquids is prevalent, elongated optical elements non-invasively operated in the shear force modus could have some specific advantages when compared to contact modus systems. While tapping mode NSOM provides satisfactory nanoscale images even on solid surfaces covered with millimetres of liquids, the performance of shear force mode NSOM is presently largely confined to operations on dry samples. This is due to the inability of conventional shear force mode NSOM systems to provide sharp topographic images of sample surfaces substantially covered with liquids. By equipping a conventional NSOM system with hydrophobic optical elements, shear force mode based topographic images could be obtained on biological samples in dry as well as in aqueous environment, and with resolutions on the nanoscale level.

Journal Article↗
PubMed1993

The development of non-retinal afferent projections to the frog optic tectum and the substance P immunoreactivity of tectal connections.

Accessibility in early development and the presence of a retinotopic map have made the amphibian optic tectum a popular system for exploration of the role of synaptic function in central map refinement. Although a great deal is known about the development of retinal innervation of the tectum, little information exists about the development of non-retinal tectal inputs. Since these other afferent systems may contribute to the synaptic drive of developing tectal cells and thereby be involved in the activity-dependent refinement of the retinotectal map, we sought to determine whether these inputs are present at the early tadpole stages when the first retinal axons refine their synaptic order within the tectal neuropil. Rhodamine-labelled latex beads, retrogradely transported from injection sites in the optic tecta, were used to identify tectal afferent projections. Projection patterns in very young tadpoles were identical to those found in juvenile frogs and heavily labelled regions included areas of the posteroventral tegmental field, the posterior tuberculum, the ventromedial thalamic nucleus, the ventral part of the ventrolateral thalamic nucleus, the suprachiasmatic nucleus and discrete regions within the central and anterior thalamic nuclei. Ipsilateral nucleus isthmi cells were also labelled, indicating the existence of an isthmo-tectal projection in even the youngest animals examined. Additionally, substance P-like immunoreactive tecto-isthmal fibers were traced from the optic tectum to the nucleus isthmi. The presence of these connections suggests that feedback from the nucleus isthmi and/or input from the other brain areas projecting to the tectum may play a role in modulating the cellular mechanisms that underlie the formation of the visual map.

Afferent Pathways↗