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Keith Langley

Publications and source records attributed to Keith Langley.

9 recordsLinked to original sources
PubMed2002

Coexpression of thyroid hormone receptor isoforms in mouse oligodendrocytes.

Double and triple immunocytochemistry with stage-specific markers and specific antireceptor antibodies was used to study expression of nuclear thyroid hormone receptor (TR) isoforms in cultured mouse oligodendrocytes. To evaluate the coexpression of each TR isoform, antibodies were raised in rabbits and mice against specific regions of alpha1-TR and alpha2-TR common to both alpha isoforms and beta1-TR. Their specificities were assessed by Western blotting and by immunocytochemistry on rat hepatocytes. Oligodendrocyte subpopulations were found to coexpress the alpha- and beta1-TR epitopes at defined developmental stages. Both alpha- and beta1-TR isoforms are colocalized in oligodendrocytes during an early stage identified by the marker OL-1, before 2',3'-cyclic nucleotide 3'-phosphohydrolase is expressed. Expression of beta1-TR varies during maturation, and that of alpha-TR decreases during terminal maturation.

Aging↗
PubMed2002

The stereoscopic anisotropy: individual differences and underlying mechanisms.

Observers are more sensitive to variations in the depth of stereoscopic surfaces in a vertical than in a horizontal direction; however, there are large individual differences in this anisotropy. The authors measured discrimination thresholds for surfaces slanted about a vertical axis or inclined about a horizontal axis for 50 observers. Orientation and spatial frequency discrimination thresholds were also measured. For most observers, thresholds were lower for inclination than for slant and lower for orientation than for spatial frequency. There was a positive correlation between the 2 anisotropies, resulting from positive correlations between (a) orientation and inclination thresholds and (b) spatial frequency and slant thresholds. These results support the notion that surface inclination and slant perception is in part limited by the sensitivity of orientation and spatial frequency mechanisms.

Anisotropy↗
PubMed2002

Motion perception and motion estimation by total-least squares.

A computational model of motion perception is proposed. The model, which is gradient-based, adheres to the neural constraint that transmitted signals are positive-valued functions by posing the estimation of image motion as a quadratic programming problem combined with total-least squares: a model that assumes that image signals are contaminated by noise in both the spatial and temporal dimensions. By shrinking motion estimates with a regularizer whose subtractive effect introduces a contrast dependent speed threshold into motion computations, it is shown that the total-least squares model when posed as a quadratic programming problem, is capable of explaining both increases and decreases in perceived speed as these effects were reported by Thompson (1982) to vary as a function of image contrast and temporal frequency. The correlation that exists between the model's contrast speed response and results reported from visual psychophysics is consistent with the view that the visual system assumes that image signals may be contaminated by noise in both the spatial and the temporal domain, and that visual motion is influenced by the consequence of these assumptions.

Humans↗
PubMed2002

Contrast adaptation may enhance contrast discrimination.

Whether contrast adaptation may enhance contrast discrimination is a question that has remained largely unresolved because of conflicting empirical evidence. Greenlee and Heitger (1988), for example, reported that contrast discrimination may be enhanced after contrast adaptation, while Maattanen and Koenderink (1991) did not. This paper aimed to account for the different conclusions reached by these independent researchers by manipulations of key differences that exist between the two studies. It is shown that contrast discrimination may be enhanced after adaptation, but that these effects can vary markedly across subjects and test conditions. Enhancements in contrast discrimination are reported to be significant when adapting and testing at low levels of contrast, but just significant at higher levels of contrast. For high contrast signals; enhancements are shown to be independent of temporal frequency but dependent upon viewing conditions. Under binocular viewing conditions, enhancements in contrast discrimination thresholds are shown to be significantly higher than under monocular viewing conditions. It is suggested that the different conclusions reached by Greenlee and Heitger and by Maattanen and Koenderink may be explained by their respective differences in viewing conditions. The former study used binocular, while the latter study used monocular viewing with an occluding eyepatch.

Adaptation, Ocular↗
PubMed2002

A parametric account of contrast adaptation on contrast perception.

The effect of contrast adaptation on perceived contrast is assessed by contrast matching spatially adjacent sinusoidal gratings of similar spatial frequency, but different contrast and orientation. The main empirical question asked is why a high contrast orthogonal adaptor appears to amplify contrast signals through an increase in the slope of the contrast matching function but does not affect the threshold contrast at which a grating is detected. To explain this effect of adaptation, the Naka- Rushton receptor equation is employed as a description of the visual system's contrast response function. It is reported that the effects of adaptation may be described by three isotropic components, namely, signal amplification, division and addition, and one orientation specific component of subtraction. By collating the predictions made by the Naka-Rushton receptor equation with existing psychophysical data, it is shown that the magnitude of the isotropic components of adaptation increase with the contrast of the adapting signal. The orientation specific effect, however, is shown to saturate at relatively low adapting contrast levels. This saturation appears to be inconsistent with the commonly held view that the orientation specific effect represents a functional strategy used by the visual system to combat the problem of neural saturation in response firing rates.

Adaptation, Ocular↗
PubMed2002

Visual adaptation.

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Adaptation, Ocular↗
PubMed1992

Noradrenergic, but not Adrenergic Chromaffin Cells in the Adrenal Gland Express Neuromodulin (GAP-43).

Neuroendocrine chromaffin cells of the adrenal gland express certain molecular markers either transiently during development or permanently. In the present study, the expression of neuromodulin (GAP-43), a neuronal protein often associated with neurite outgrowth, was examined in adult adrenals. Neuromodulin was detected by Western blot analysis in extracts of both rat adrenals and cultured bovine chromaffin cells, and was localized in situ in a subpopulation of chromaffin cells, as well as in nerve fibres and Schwann cells. The use of anti-tyrosine hydroxylase or anti-phenylethanolamine N-methyltransferase antibodies in combination with anti-neuromodulin antibodies in double immunofluorescent labelling of cryostat sections of rat glands demonstrated that neuromodulin is expressed by noradrenergic, and not by adrenergic chromaffin cells. The results provide further evidence that neuromodulin is not limited to neurons; it is also expressed in a subpopulation of neuroendocrine chromaffin cells. Neuromodulin may play a role in the development of the adrenal medulla or in the specific regulation of noradrenalin secretion from chromaffin cells.

Journal Article↗
PubMed1992

L1 Cell Adhesion Molecule is Expressed by Noradrenergic but not Adrenergic Chromaffin Cells: A Possible Major Role for L1 in Adrenal Medullary Design.

The adrenal medulla of higher animals is constituted of homotypic groups of chromaffin cells secreting either adrenalin or noradrenalin. Since not all chromaffin cells are individually innervated by fibres of the splanchnic nerve, this tissue characteristic is crucial to the physiological function of the gland. In an attempt to analyse differences between these chromaffin cell types which might underlie the establishment of this tissue pattern, we examined the expression of the adhesion molecule L1 in this gland by immunocytochemistry at the optical and ultrastructural levels in rats. L1, an adhesion molecule abundant in the central nervous system, was found to be present in the adrenal medulla of adults; it was strongly expressed on innervating axons and their surrounding Schwann cells and also on a subpopulation of chromaffin cells. The nature of these chromaffin cells was examined by immunocytochemistry using antibodies against the catecholamine-synthesizing enzyme phenylethanolamine N-methyltransferase (PNMT), which are capable of distinguishing between adrenergic and noradrenergic cells. Immunofluorescence labelling of sequential frozen sections demonstrated that chromaffin cells which express L1 do not express PNMT; conversely, L1 was not detected in any chromaffin cells expressing PNMT. Ultrastructural immunocytochemistry confirmed the existence of two non-overlapping populations of chromaffin cells. It is concluded that, in the adrenal medulla, noradrenergic but not adrenergic chromaffin cells express this adhesion molecule. These data, together with our previous observations that all chromaffin cells express the neural cell adhesion molecule, NCAM, suggest that L1, in cooperation with NCAM, could be responsible for the association of noradrenergic cells in the form of homotypic aggregates segregated from groups of adrenergic cells within the adrenal medulla.

Journal Article↗