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Biomedical subjects

Y Usson

Publications and source records attributed to Y Usson.

58 records · Page 4Linked to original sources

Differential growth of sensory neurons in vitro in presence of dermis and epidermis. A quantitative time-lapse analysis.

The influence of dermal and epidermal cells on the growth of nerve fibres from chick embryo sensory neurons was investigated in vitro. A previous quantitative analysis showed that the growth of nerve fibres is profoundly modified in the close vicinity of epidermis. This change is mainly characterized by erratic trajectories of nerve fibres resulting from numerous lateral displacements of the growth cones. In contrast, no such behaviour is observed far away from the epidermis or in the presence of dermis. In this latter case, neurites exhibit a straighter direction of extension. These observations suggest that the epidermis exerts some kind of control on the establishment of nerve fibre pattern in the dermis.

Animals↗

Multimodal frequency distribution analysis of peripheral nerves.

In morphometric studies of peripheral nerves, the statistical analysis of such data as axon diameters is complicated by the presence of multimodal distributions. Nerve fiber diameters, for example, cannot be analyzed by classical parametric tests, and such descriptive statistics as mean or variance lose much of their usefulness. The recent development of stochastic catastrophe models offers a new parametric tool with which to describe multimodal distributions. This paper describes our development of a PASCAL computer program that permitted the modelling, comparison and segmentation of multimodal distributions. The method is based on a description of the multimodal frequency distributions by probability density functions of the canonical exponential family.

Axons↗

In vitro angiogenesis is modulated by the mechanical properties of fibrin gels and is related to alpha(v)beta3 integrin localization.

This study deals with the role of the mechanical properties of matrices in in vitro angiogenesis. The ability of rigid fibrinogen matrices with fibrin gels to promote capillarylike structures was compared. The role of the mechanical properties of the fibrin gels was assessed by varying concentration of the fibrin gels. When the concentration of fibrin gels was decreased from 2 mg/ml to 0.5 mg/ml, the capillarylike network increased. On rigid fibrinogen matrices, capillarylike structures were not formed. The extent of the capillarylike network formed on fibrin gels having the lowest concentration depended on the number of cells seeded. The dynamic analysis of capillarylike network formation permitted a direct visualization of a progressive stretching of the 0.5 mg/ml fibrin gels. This stretching was not observed when fibrin concentration increases. This analysis shows that 10 h after seeding, a prearrangement of cells into ringlike structures was observed. These ringlike structures grew in size. Between 16 and 24 h after seeding, the capillarylike structures were formed at the junction of two ringlike structures. Analysis of the alpha(v)beta3 integrin localization demonstrates that cell adhesion to fibrinogen is mediated through the alpha(v)beta3 integrin localized into adhesion plaques. Conversely, cell adhesion to fibrin shows a diffuse and dot-contact distribution. We suggest that the balance of the stresses between the tractions exerted by the cells and the resistance of the fibrin gels triggers an angiogenic signal into the intracellular compartment. This signal could be associated with modification in the alpha(v)beta3 integrin distribution.

Biomechanical Phenomena↗

Method for 3D volumetric analysis of intranuclear fluorescence distribution in confocal microscopy.

The introduction of the confocal laser scanning microscope makes it possible to acquire fluorescent specimens in 3D. We present basic image processing tools to enhance the data and to quantitate the morphology and topography of the intravolume elements. The tools were applied to the description of the spatial distribution of DNA replication sites in mammalian cell nuclei as an example.

Algorithms↗