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K. I. Mazzitello

Publications and source records attributed to K. I. Mazzitello.

3 recordsLinked to original sources

Druse-Induced Morphology Evolution in Retinal Pigment Epithelium

The retinal pigment epithelium (RPE) is a key site of pathogenesis for many retina diseases. The formation of drusen in the retina is characteristic of retinal degeneration. We investigate morphological changes in the RPE in the presence of soft drusen using an integrated experimental and modeling approach. We collect RPE flat mount images from donated human eyes and develop 1) statistical tools to quantify the images and 2) a cell-based model to simulate the morphology evolution. We compare three different mechanisms of RPE repair evolution, cell apoptosis, cell fusion, and expansion, and Simulations of our RPE morphogenesis model quantitatively reproduce deformations of human RPE morphology due to drusen, suggesting that a purse-string mechanism is sufficient to explain how RPE heals cell loss caused by drusen-damage. We found that drusen beneath tissue promote cell death in a number that far exceeds the cell numbers covering the drusen. Tissue deformations are studied using area distributions, Voronoi domains and a texture tensor.

q-bio.TO

Low-coverage heteroepitaxial growth with interfacial mixing

We investigate the influence of intermixing on heteroepitaxial growth dynamics, using a two-dimensional point island model, expected to be a good approximation in the early stages of epitaxy. In this model, which we explore both analytically and numerically, every deposited B atom diffuses on the surface with diffusion constant $D_{\rm B}$, and can exchange with any A atom of the substrate at constant rate. There is no exchange back, and emerging atoms diffuse on the surface with diffusion constant $D_{\rm A}$. When any two diffusing atoms meet, they nucleate a point island. The islands neither diffuse nor break, and grow by capturing other diffusing atoms. The model leads to an island density governed by the diffusion of one of the species at low temperature, and by the diffusion of the other at high temperature. We show that these limit behaviors, as well as intermediate ones, all belong to the same universality class, described by a scaling law. We also show that the island-size distribution is self-similarly described by a dynamic scaling law in the limits where only one diffusion constant is relevant to the dynamics, and that this law is affected when both $D_{\rm A}$ and $D_{\rm B}$ play a role.

cond-mat.stat-mech

Converting genetic network oscillations into somite spatial pattern

In most vertebrate species, the body axis is generated by the formation of repeated transient structures called somites. This spatial periodicity in somitogenesis has been related to the temporally sustained oscillations in certain mRNAs and their associated gene products in the cells forming the presomatic mesoderm. The mechanism underlying these oscillations have been identified as due to the delays involved in the synthesis of mRNA and translation into protein molecules [J. Lewis, Current Biol. {\bf 13}, 1398 (2003)]. In addition, in the zebrafish embryo intercellular Notch signalling couples these oscillators and a longitudinal positional information signal in the form of an Fgf8 gradient exists that could be used to transform these coupled temporal oscillations into the observed spatial periodicity of somites. Here we consider a simple model based on this known biology and study its consequences for somitogenesis. Comparison is made with the known properties of somite formation in the zebrafish embryo . We also study the effects of localized Fgf8 perturbations on somite patterning.

q-bio.QM