波音游戏-波音娱乐城赌球打不开

ABSTRACT

We develop a Voronoi cell-based model of epithelial cell dynamics and apply it to two different phenomena: (1) the regulation of the cornea, and (2) potential pathways for the evolution of cancer.

In the first model, we consider the cornea, which is a stratified epithelium consisting of several layers, each only one cell thick.  Maintaining this structure is essential for high-quality vision.  Furthermore, the cornea regenerates itself from a ring of stem cells at the bottom, or basal, layer through a process of stem cell division and proliferation of cells in the basal layer, centripetal cell migration, and delamination of cells from one layer to the layer above.  In mice, corneal tissue turns over in about only two weeks, and human corneas turn over similarly rapidly.  Despite its importance, little is known about what regulates this process and how it adjusts to cell loss due to shearing, or rubbing, and wound healing.  We seek to shed light into corneal cell regulation using a Voronoi cell-based model, linking local interactions between cells to the emergent dynamics of the stratified epithelium. In the second model, we use our Voronoi model to consider the development of cancer.  A common paradigm for cancer evolution is that cells acquire a series of mutations producing increasingly malignant clones that outcompete other populations in a process known as lineal evolution.  However, recent experiments observe that many tumours remain polyclonal, conflicting with the idea of a single dominant clone. We propose an alternative paradigm of interclonal cooperativity in which individually nonmalignant clones, cooperate to produce a collectively malignant cancer population.  We consider two key phenotypes involved in the transition to malignancy, namely increased growth and increased motility, and investigate the emergent dynamics of the paradigms using Voronoi cell-based modelling.  Using our models, we investigate conditions that enable cells acquiring cooperative mutations, in contrast to cell-autonomous mutations, to give rise to polyclonal tumours. This is a joint work with Neda Khodabakhsh Joniani, Mst. Shanta Khatun, J. Guy Lyons.