Thermo-Mixed Hydrodynamics of Piston Compression Ring Conjunction

The final publication is available at http://link.springer.com.A new method, comprising Navier-Stokes equations, Rayleigh-Plesset volume fraction equation, an analytical control-volume thermal mixed approach and asperity interactions is reported. The method is employed for prediction of lubricant flow and assessment of friction in the compression ring-cylinder liner conjunction. The results are compared with Reynolds-based laminar flow with Elrod cavitation algorithm. Good conformance is observed for medium load intensity part of the engine cycle. At lighter loads and higher sliding velocity, the new method shows more complex fluid flow, possessing layered flow characteristics on account of pressure and temperature gradient into the depth of the lubricant film, which leads to a cavitation region with vapour content at varied volume fractions. Predictions also conform well to experimental measurements reported by other authors

Rodent models of focal cerebral ischemia: procedural pitfalls and translational problems

Rodent models of focal cerebral ischemia are essential tools in experimental stroke research. They have added tremendously to our understanding of injury mechanisms in stroke and have helped to identify potential therapeutic targets. A plethora of substances, however, in particular an overwhelming number of putative neuroprotective agents, have been shown to be effective in preclinical stroke research, but have failed in clinical trials. A lot of factors may have contributed to this failure of translation from bench to bedside. Often, deficits in the quality of experimental stroke research seem to be involved. In this article, we review the commonest rodent models of focal cerebral ischemia - middle cerebral artery occlusion, photothrombosis, and embolic stroke models - with their respective advantages and problems, and we address the issue of quality in preclinical stroke modeling as well as potential reasons for translational failure

Cancer Biomarker Discovery: The Entropic Hallmark

Background: It is a commonly accepted belief that cancer cells modify their transcriptional state during the progression of the disease. We propose that the progression of cancer cells towards malignant phenotypes can be efficiently tracked using high-throughput technologies that follow the gradual changes observed in the gene expression profiles by employing Shannon's mathematical theory of communication. Methods based on Information Theory can then quantify the divergence of cancer cells' transcriptional profiles from those of normally appearing cells of the originating tissues. The relevance of the proposed methods can be evaluated using microarray datasets available in the public domain but the method is in principle applicable to other high-throughput methods. Methodology/Principal Findings: Using melanoma and prostate cancer datasets we illustrate how it is possible to employ Shannon Entropy and the Jensen-Shannon divergence to trace the transcriptional changes progression of the disease. We establish how the variations of these two measures correlate with established biomarkers of cancer progression. The Information Theory measures allow us to identify novel biomarkers for both progressive and relatively more sudden transcriptional changes leading to malignant phenotypes. At the same time, the methodology was able to validate a large number of genes and processes that seem to be implicated in the progression of melanoma and prostate cancer. Conclusions/Significance: We thus present a quantitative guiding rule, a new unifying hallmark of cancer: the cancer cell's transcriptome changes lead to measurable observed transitions of Normalized Shannon Entropy values (as measured by high-throughput technologies). At the same time, tumor cells increment their divergence from the normal tissue profile increasing their disorder via creation of states that we might not directly measure. This unifying hallmark allows, via the the Jensen-Shannon divergence, to identify the arrow of time of the processes from the gene expression profiles, and helps to map the phenotypical and molecular hallmarks of specific cancer subtypes. The deep mathematical basis of the approach allows us to suggest that this principle is, hopefully, of general applicability for other diseases

Differentiation, growth and morphogenesis: Acetabularia as a model system

The aim of this paper is to review the present knowledge of the main aspects of differentiation of Acetabularia, a unicellular, eukaryotic organism, and to underline the multiple control pathways modulated by circadian rhythmicity. Growth and morphogenesis are sequentially programmed. Timing of cap differentiation is highly dependent on external conditions. The importance of the sequence of processes is shown by experimental disregulation. The alga is a highly polarized cell, both in morphology and in the relative concentrations of a number of the molecules it contains. Apical cap differentiation is regulated at the post-transcriptional level and could also depend in part on polyamines and on proteolytic activity. Acetabularia displays a number of circadian rhythms (CR). These rhythms form an elaborate biological time structure (also called temporal morphology, or morphology in time as opposed to morphology in space): the distribution in the 24 h cycle of the peaks and troughs of the oscillating functions. The oscillations display fixed relations both with the other functions and with external conditions (such as the transition from dark to light). Interestingly, the CR modulate Acetabularia's development, which is influenced by photoperiod; we present preliminary experiments suggesting that disruption of temporal morphology is deleterious to morphogenesis. Induction of growth and of morphogenesis are totally dependent on blue light. However, blue light receptors in plants are probably multiple, but we present arguments suggesting that flavin-cytochrome b and the associated SHAM-sensitive molecule are present in Acetabularia plasma membrane and are involved in blue light perception. Agents interfering with different steps of signal perception and transduction show that at least some of these steps are temporally regulated. According to recent experiments from our laboratory, the existence of a redox signalling mechanism appears to be highly probable. The phytohormones (or plant regulators), auxin (indole acetic acid), abscisic acid and ethylene, exert cell-regulatory functions and are involved in Acetabularia differentiation. They also modulate at least some circadian rhythms. Finally, circadian rhythms intervene in differentiation and are proposed to have an integrative function.SCOPUS: re.jFLWINinfo:eu-repo/semantics/publishe