Protective effects of <Emphasis Type="SmallCaps">l</Emphasis>-selenomethionine on space radiation induced changes in gene expression

Ionizing radiation can produce adverse biological effects in astronauts during space travel. Of particular concern are the types of radiation from highly energetic, heavy, charged particles known as HZE particles. The aims of our studies are to characterize HZE particle radiation induced biological effects and evaluate the effects of l-selenomethionine (SeM) on these adverse biological effects. In this study, microarray technology was used to measure HZE radiation induced changes in gene expression, as well as to evaluate modulation of these changes by SeM. Human thyroid epithelial cells (HTori-3) were irradiated (1 GeV/n iron ions) in the presence or in the absence of 5 μM SeM. At 6 h post-irradiation, all cells were harvested for RNA isolation. Gene Chip U133Av2 from Affymetrix was used for the analysis of gene expression, and ANOVA and EASE were used for a determination of the genes and biological processes whose differential expression is statistically significant. Results of this microarray study indicate that exposure to small doses of radiation from HZE particles, 10 and 20 cGy from iron ions, induces statistically significant differential expression of 196 and 610 genes, respectively. In the presence of SeM, differential expression of 77 out of 196 genes (exposure to 10 cGy) and 336 out of 610 genes (exposure to 20 cGy) is abolished. In the presence or in the absence of SeM, radiation from HZE particles induces differential expression of genes whose products have roles in the induction of G1/S arrest during the mitotic cell cycle, as well as heat shock proteins. Some of the genes, whose expressions were affected by radiation from HZE particles and were unchanged in irradiated cells treated with SeM, have been shown to have altered expression levels in cancer cells. The conclusions of this report are that radiation from HZE particles can induce differential expression of many genes, some of which are known to play roles in the same processes that have been shown to be activated in cells exposed to radiation from photons (like cell cycle arrest in G1/S), and that supplementation with SeM abolishes HZE particle-induced differential expression of many genes. Understanding the roles that these genes play in the radiation-induced transformation of cells may help to decipher the origins of radiation-induced cancer.     

Risk calculations for hereditary effects of ionizing radiation in humans

Summary A prediction of the extent to which an additional dose of ionizing radiation increases the natural germ cell mutation rate, and how much such an increase will affect the health status of future human populations is part of the service that human geneticists are expected to offer to human society. However, more detailed scrutiny of the difficulties involved reveals an extremely complex set of problems. A large number of questions arises before such a prediction can be given with confidence; many such questions cannot be answered at our present state of knowledge. However, such predictions have recently been attempted. The 1988 report of the United Nations Scientific Committee for the Effects of Atomic Radiation and the fifth report of the Committee on Biological Effects of Ionizing Radiation of the US National Research Council have presented a discussion of the human genetics problems involved. Empirical data from studies on children of highly radiation-exposed parents, e.g. parents exposed to the atomic bombs of Hiroshima and Nagasaki, or parents belonging to populations living on soil with high background radiation, have been mentioned in this context. Whereas precise predictions are impossible as yet because of deficiencies in our knowledge of medical genetics at various levels, the bulk of the existing evidence points to only small effects of low or moderate radiation doses, effects that will probably be buried in the background noise of changing patterns of human morbidity and mortality.     

Utilization of Plasmonic and Photonic Crystal Nanostructures for Enhanced Micro- and Nanoparticle Manipulation

A method to manipulate the position and orientation of submicron particles nondestructively would be an incredibly useful tool for basic biological research. Perhaps the most widely used physical force to achieve noninvasive manipulation of small particles has been dielectrophoresis(DEP).¹ However, DEP on its own lacks the versatility and precision that are desired when manipulating cells since it is traditionally done with stationary electrodes. Optical tweezers, which utilize a three dimensional electromagnetic field gradient to exert forces on small particles, achieve this desired versatility and precision.² However, a major drawback of this approach is the high radiation intensity required to achieve the necessary force to trap a particle which can damage biological samples.³ A solution that allows trapping and sorting with lower optical intensities are optoelectronic tweezers (OET) but OET''s have limitations with fine manipulation of small particles; being DEP-based technology also puts constraint on the property of the solution.^4,5This video article will describe two methods that decrease the intensity of the radiation needed for optical manipulation of living cells and also describe a method for orientation control. The first method is plasmonic tweezers which use a random gold nanoparticle (AuNP) array as a substrate for the sample as shown in Figure 1. The AuNP array converts the incident photons into localized surface plasmons (LSP) which consist of resonant dipole moments that radiate and generate a patterned radiation field with a large gradient in the cell solution. Initial work on surface plasmon enhanced trapping by Righini et al and our own modeling have shown the fields generated by the plasmonic substrate reduce the initial intensity required by enhancing the gradient field that traps the particle.^6,7,8 The plasmonic approach allows for fine orientation control of ellipsoidal particles and cells with low optical intensities because of more efficient optical energy conversion into mechanical energy and a dipole-dependent radiation field. These fields are shown in figure 2 and the low trapping intensities are detailed in figures 4 and 5. The main problems with plasmonic tweezers are that the LSP''s generate a considerable amount of heat and the trapping is only two dimensional. This heat generates convective flows and thermophoresis which can be powerful enough to expel submicron particles from the trap.^9,10 The second approach that we will describe is utilizing periodic dielectric nanostructures to scatter incident light very efficiently into diffraction modes, as shown in figure 6.¹¹ Ideally, one would make this structure out of a dielectric material to avoid the same heating problems experienced with the plasmonic tweezers but in our approach an aluminum-coated diffraction grating is used as a one-dimensional periodic dielectric nanostructure. Although it is not a semiconductor, it did not experience significant heating and effectively trapped small particles with low trapping intensities, as shown in figure 7. Alignment of particles with the grating substrate conceptually validates the proposition that a 2-D photonic crystal could allow precise rotation of non-spherical micron sized particles.¹⁰ The efficiencies of these optical traps are increased due to the enhanced fields produced by the nanostructures described in this paper.Download video file.^{(57M, mov)}     

Damage to cellular DNA from particulate radiations,the efficacy of its processing and the radiosensitivity of mammalian cells

Summary For several years, it has been evident that cellular radiation biology is in a necessary period of consolidation and transition (Lett 1987, 1990; Lett et al. 1986, 1987). Both changes are moving apace, and have been stimulated by studies with heavy charged particles.From the standpoint of radiation chemistry, there is now a consensus of opinion that the DNA hydration shell must be distinguished from bulk water in the cell nucleus and treated as an integral part of DNA (chromatin) (Lett 1987). Concomitantly, sentiment is strengthening for the abandonment of the classical notions of direct and indirect action (Fielden and O'Neill 1991; O'Neill 1991; O'Neill et al. 1991; Schulte-Frohlinde and Bothe 1991 and references therein). A layer of water molecules outside, or in the outer edge of, the DNA (chromatin) hydration shell influences cellular radiosensitivity in ways not fully understood. Charge and energy transfer processes facilitated by, or involving, DNA hydration must be considered in rigorous theories of radiation action on cells. The induction and processing of double stand breaks (DSBs) in DNA (chromatin) seem to be the predominant determinants of the radiotoxicity of normally radioresistant mammalian cells, the survival curves of which reflect the patterns of damage induced and the damage present after processing ceases, and can be modelled in formal terms by the use of reaction (enzyme) kinetics. Incongruities such as sublethal damage are neither scientifically sound nor relevant to cellular radiation biology (Calkins 1991; Lett 1990; Lett et al. 1987a).Increases in linear energy transfer (LET) up to 100–200 keV µm^–1 cause increases in the extents of neighboring chemical and physical damage in DNA denoted by the general term DSB. Those changes are accompanied by decreasing abilities of cells normally radioresistant to sparsely ionizing radiations to process DSBs in DNA and chromatin and to recover from radiation exposure, so they make significant contributions to the relative biological effectiveness (RBE) of a given radiation. As the LET is raised above a few hundred keV µm^–1, the damage associated with DSBs continues to increase, but the efficiency of DSB induction declines to low values (0.1), as do RBE and the effective processing of DSBs and chromatin breaks, and the decline in RBE seems to mimic the overall decline in suitable processing of DSBs. Hence, the quality factor (Q) for a given radiation cannot be based solely upon the pattern of energy deposition, a fact attested to also by the quite different RBE responses exhibited by repair-deficient mutant (or variant) cells.Understanding of the biological effects of heavy ions is important not only for the welfare of astronauts who will undertake extended interplanetary missions in space but also for the facilitation of a rigorous scientific basis for conventional radiation therapy.Based on a review lecture delivered at the Fourth Workshop on Heavy Charged Particles in Biology and Medicine, GSl, Darmstadt, Germany, September 1991. A number of scientists, see Acknowledgements, also gave unreservedly of their time at the 40th Annual Meeting of the Radiation Research Society, Salt Lake City, Utah, March 1992, to discuss topics in this article with the author     

Heavy charged particles produce a bystander effect via cell-cell junctions.

Radiation-induced damage to living cells results from either a direct hit to cellular DNA, or from indirect action which leads to DNA damage from radiation produced radicals. However, in recent years there is evidence that biological effects such as cell killing, mutation induction, chromosomal damage and modification of gene expression can occur in a cell population exposed to low doses of alpha particles. In fact these doses are so low that not all cells in the population will be hit directly by the radiation. Using a precision alpha-particle microbeam, it has been recently demonstrated that irradiated target cells can induce a bystander mutagenic response in neighboring "bystander" cells which were not directly hit by alpha particles. Furthermore, these results suggest that gap-junction mediated cell-to-cell communication plays a critical role in this bystander phenomenon. The purpose of this section is to describe recent studies on bystander biological effects. The recent work described here utilized heavy charged particles for irradiation, and investigated the role of gap-junction mediated cell-cell communication in this phenomenon.     

Learning and recall in a dynamic theory of coordination patterns

A dynamic theory of learning and recall of coordination patterns is developed in the context of relative timing skills. Characterizing the coordination patterns in such skills by the collective variable, relative phase, we choose a model system in which the intrinsic pattern dynamics as well as the influence of environmental and memorized information are well understood from previous experimental and theoretical work. To describe learning we endow memorized information with dynamics which is determined by a phenomenological strategy. Similarly, additional degrees of freedom must be introduced to understand recall. As such recall variables we choose the relative strengths with which each memorized pattern acts on the pattern dynamics and model their dynamics phenomenologically. The resulting dynamical system that resembles models used in pattern recognition theory is shown to adequately describe the learning and recall processes. Moreover, due to the operational character of the theory, several predictions emerge that are open to experimental test. In particular, we show under which conditions phase transitions occur in the dynamics of the coordination patterns during learning and during recall. Considering different time scales and their relations we demonstrate how these phase transitions can be identified and observed. Other predictions include the influence of the intrinsic pattern dynamics on the recall process and the existence of history and hysteresis effects in recall. We discuss different forms of forgetting and differentiation of memorized information. The results show how a new theoretical view of learning and recall as change of behavioral dynamics can lead to a different understanding of these processes by providing testable predictions.     

Response of pioneer soil microalgal colonists to environmental change in Antarctica

There is increasing evidence of climate change in Antarctica, especially elevated temperature and ultraviolet B (UVB) flux within the ozone hole. Its origins are debatable, but the effects on ice recession, water availability, and summer growth conditions are demonstrable. Light-dependent, temperature-sensitive, fast-growing organisms respond to these physical and biogeographical changes. Microalgae (cyanobacteria and eukaryotic algae), which are pioneer colonists of Antarctic mineral fellfield soils, are therefore highly suitable biological indicators of such changes. In frost-heaved soil polygons containing naturally sorted fine mineral particles, microalgal growth is restricted to a shallow zone of light penetration. By virtue of this light requirement, microalgae are exposed to extreme seasonal fluctuations in temperature (air and black-body radiation), photosynthetically active radiation, UV radiation, and desiccation. Dominance of conspicuous autofluorescent indicator species with distinctive morphology allowed quantification of responses using epifluorescence microscopy, and image analysis of undisturbed, unstained communities. However, the physical changes in climate, although significant in the long term, are gradual. The changes were therefore amplified experimentally by enclosing the communities at a fellfield site on Signy Island, maritime Antarctica, in cloches (small greenhouses). These were made of polystyrene of either UV transparent or UV opaque acrylic plastic, with or without walls. During a 6-year period, statistically significant changes were observed in microalgal colonization of the soil surface and in the morphology of filamentous populations. Evidence of community succession correlated with measured changes in local environment was found. Results from Signy Island and at continental sites on Alexander Island suggested that rates of microalgal colonization and community development might change significantly during current climate changes in Antarctica. Correspondence to: D.D. Wynn-Williams.     

Chemical and biological consequences ofβ-decay

Summary In Part 1 of this article physical and chemical effects of-decay in labelled molecules were reviewed and their potential importance for breaking predetermined and specific bonds were pointed out. After incorporation of labelled biomolecules in living systems, such as viruses, phages or cells, the radioactive decay of the label alters the biological behaviour of the system, in the extreme case causing loss of the ability to reproduce, the extent of these consequences depending strongly on the type of radioisotope.Now Part 2 includes a brief discussion of biological effects associated with-decay, emphasizing the relative importance of local transmutation and internal radiation effects from the decay of³H,¹⁴C,³²P,³³P,³⁵S and¹²⁵I. Attempt is also made, whenever possible at the present stage of understanding, to correlate biological effects with chemical processes on a molecular level.     

Phosphoproteomics profiling of human skin fibroblast cells reveals pathways and proteins affected by low doses of ionizing radiation

Background

High doses of ionizing radiation result in biological damage; however, the precise relationships between long-term health effects, including cancer, and low-dose exposures remain poorly understood and are currently extrapolated using high-dose exposure data. Identifying the signaling pathways and individual proteins affected at the post-translational level by radiation should shed valuable insight into the molecular mechanisms that regulate dose-dependent responses to radiation.

Principal Findings

We have identified 7117 unique phosphopeptides (2566 phosphoproteins) from control and irradiated (2 and 50 cGy) primary human skin fibroblasts 1 h post-exposure. Semi-quantitative label-free analyses were performed to identify phosphopeptides that are apparently altered by radiation exposure. This screen identified phosphorylation sites on proteins with known roles in radiation responses including TP53BP1 as well as previously unidentified radiation-responsive proteins such as the candidate tumor suppressor SASH1. Bioinformatic analyses suggest that low and high doses of radiation affect both overlapping and unique biological processes and suggest a role for MAP kinase and protein kinase A (PKA) signaling in the radiation response as well as differential regulation of p53 networks at low and high doses of radiation.

Conclusions

Our results represent the most comprehensive analysis of the phosphoproteomes of human primary fibroblasts exposed to multiple doses of ionizing radiation published to date and provide a basis for the systems-level identification of biological processes, molecular pathways and individual proteins regulated in a dose dependent manner by ionizing radiation. Further study of these modified proteins and affected networks should help to define the molecular mechanisms that regulate biological responses to radiation at different radiation doses and elucidate the impact of low-dose radiation exposure on human health.     

Siberian plants: untapped repertoire of bioactive endosymbionts

Background

Endosymbionts are microorganisms present in all plant species, and constitute the subject of interest among the scientific community. These symbionts have gained considerable attention in recent years, owing to their emerging biological roles. Global challenges, such as antimicrobial resistance, treatment of infectious diseases such as HIV and tuberculosis, cancer, and many genetic disorders, exist. Endosymbionts can help address these challenges by secreting valueadded bioactive compounds with various activities.

Objective

Herein, we describe the importance of plants inhabiting Siberian niches. These plants are considered to be among the least studied organisms in the plant kingdom worldwide. Barcoding these plants can be of interest for exploring bioactive endosymbionts possessing myriad biological properties.

Methods

A systematic survey of relevant scientific reports was conducted using the PubMed search engine. The reports were analyzed, and compiled to draft this review.

Results

The literature survey on Siberian plants regarding endosymbionts included a few reports, since extremely few exploratory studies have been conducted on the plants in these regions. Studies on the endosymbionts of these plants are highly valuable, as they report potent endosymbionts possessing numerous biological properties. Based on these considerations, this review aims to create awareness among the global scientific community working on related areas.

Conclusion

This review could provide the basis for barcoding novel endosymbionts of Siberian plants and their ecological importance, which can be exploited in various sectors. The main purpose of this review is to create awareness of Siberian plants, which are among the least studied organisms in the plant kingdom, with respect to endosymbionts, among the scientific community.

     

On predictions and laws in biological evolution: Is biology able to formulate general laws and develop inductive predictions as in physics or chemistry?

Biology has so far had difficulties formulating general laws akin to physics and chemistry. Evolution and its propensity to reduce entropy could become a start for such laws in biology. Subject Categories: Evolution & Ecology, History & Philosophy of Science

Science uses evidence‐based inductive reasoning to build theories, principles, and laws. A common type of inductive reasoning is generalization, that is, projecting conclusions drawn from one or a few case studies onto a broader context. The reliability of generalizations depends upon the representativeness and the formal validation of the selected case studies, which is usually performed by hypothesis testing. Another usual type of inductive reasoning is prediction, which uses observations to develop general principles and laws that can predict or anticipate future outcomes. The reliability of these predictions is confirmed by the accomplishment of the anticipated situation. It is interesting to note that generalizations are based on the analysis of empirical evidence, whereas predictions are formulated before the desired empirical evidence, which is actually the target of the prediction, is available.

… generalizations are based on the analysis of empirical evidence, whereas predictions are formulated before the desired empirical evidence, which is actually the target of the prediction, is available.

The American philosopher of science Peter Lipton (2005) commented that we are commonly more impressed by predictions than by accommodations, as he called hypothesis testing. To illustrate this, Lipton used the discovery of Halley''s Comet. In 1705, the British astronomer Edmond Halley proposed that the comets observed in 1531, 1607, and 1682 were actually the same comet with a periodic elliptical orbit. Back then, his hypothesis did not have much impact within the scientific community. However, when Halley''s prediction was confirmed in 1758 by the return of the comet, the intellectual world in Europe widely accepted the existence of a single comet, which was subsequently named Halley''s Comet. Halley''s prediction may seem straightforward, even trivial, considering the characteristic periodicity of 75 years in previous observations. Yet, it was the predictive success, rather than prior observations, that convinced the scientific community of his conclusion.Physics is considered one of the strongest branches of science—along with chemistry and mathematics—in regard to the generality and accuracy of its predictions. Biology seems still to be in its infancy, and the search for regularities that could lend to potential generalizations is the most common approach (Dodds, 2009). This is due in part to the high level of complexity of the living world, its evolutionary change over time, and its relationships with the environment. As emphasized by the German evolutionary biologist Ernst Mayr (2004), these intrinsic and unique features of living beings, which are intimately associated with the genetic code, clearly differentiate biology from other natural sciences and make the fundamental laws of physics and chemistry insufficient to understand the living world.The main aim of this essay is to discuss whether biological research is able to develop inductive predictions similar to physics or chemistry. First, I present some classical examples of physical and chemical discoveries based on inductive predictions, such as the Higgs boson, interstellar dark matter, and the periodic table of elements. As all these advances are based on the previous existence of fundamental laws, the question arises whether similar laws exist in biology to support physics‐like inductive predictions. I suggest that, if these laws exist, they should emerge from the evolutionary process, which is the main biological singularity. Thus, it should be possible to make inductive predictions based on the fossil record, which is the fundamental evolutionary evidence. Indeed, it seems that the lack of evolutionary laws is the main drawback for inductive prediction in studying evolution, which cannot escape to Lipton’s accommodation procedures, that is, hypothesis testing and generalization.

Physics is considered one of the strongest branches of science – along with chemistry and mathematics – in regard to the generality and accuracy of its predictions.

     

Research,capacity-building and empowerment for sustainable management of African wetland ecosystems

African wetlands have important functions and values in terms of the water cycle, water quality management and biodiversity conservation. Especially relevant is their importance in food security, the provision of tradable products, and cultural and aesthetic values for local riparian communities.In Africa, knowledge of the processes, functions and values of wetlands is slim: indeed, in many regions, wetland inventories are yet to be produced. A research strategy is proposed to address some of these issues recommending an intrinsically linked, two-pronged approach: i.e. (i) studies for inventories, assessment and monitoring of wetlands and (ii) research into processes, structure and functioning of wetland ecosystems. The former has an immediate urgency whilst the latter has a long-term perspective. It is argued that curiosity-driven, (basic) research should go hand-in-hand with problem-orientated (applied) studies. Basic research is essential for a nation's scientific and technical empowerment and development. Priority topics include studies on biological diversity and integrated studies on wetlands and water resources (including water quality and the functions and values of wetland buffers).There is clear evidence of a shortage of expertise from within Africa for these topics and the reasons are discussed. Amongst others, blame is directed towards aid strategies from the industrial North and individual research programmes by `Northern' scientists in Africa. However, commitment in Africa to the actual process of scientific research is also wanting. Overall, the North have failed to stimulate a critical mass for research whilst the South suffer from a lack of momentum and from chronic under-investment.A research, training and capacity-building scheme is presented as a viable option for ameliorating the dearth of wetland resource professionals in Africa in which partnerships and networking of institutes from the North and South is encouraged.     

Estimation of the contribution of ionization and excitation to the lethal effect of ionizing radiation

Summary A simple theoretical model is proposed for estimating the differential contribution of ionization and excitation to the lethal effect of ionizing radiation. Numerical results were obtained on the basis of published experimental data on the ability of bacterial cellsEscherichia coli to undergo photoreactivation of radiation-induced damage. It was shown that inactivation by excitation may be highly significant for UV-hypersensitive cells capable of photoreactivation; inactivation by excitation increased with the energy of ionizing radiation and the volume of irradiated suspensions. The data are in qualitative agreement with the assumption of a possible contribution of the UV-component of erenkov radiation to the formation of excitations responsible for the lethal effect and the phenomenon of photoreactivation after ionizing radiation. Some predictions from the model are discussed.     

Design and integration of a problem-based biofabrication course into an undergraduate biomedical engineering curriculum

Background

The rapidly evolving discipline of biological and biomedical engineering requires adaptive instructional approaches that teach students to target and solve multi-pronged and ill-structured problems at the cutting edge of scientific research. Here we present a modular approach to designing a lab-based course in the emerging field of biofabrication and biological design, leading to a final capstone design project that requires students to formulate and test a hypothesis using the scientific method.

Results

Students were assessed on a range of metrics designed to evaluate the format of the course, the efficacy of the format for teaching new topics and concepts, and the depth of the contribution this course made to students training for biological engineering careers. The evaluation showed that the problem-based format of the course was well suited to teaching students how to use the scientific method to investigate and uncover the fundamental biological design rules that govern the field of biofabrication.

Conclusions

We show that this approach is an efficient and effective method of translating emergent scientific principles from the lab bench to the classroom and training the next generation of biological and biomedical engineers for careers as researchers and industry practicians.

     

How radiation influences atherosclerotic plaque development: a biophysical approach in ApoE ¯/¯ mice

Atherosclerosis is the development of lipid-laden plaques in arteries and is nowadays considered as an inflammatory disease. It has been shown that high doses of ionizing radiation, as used in radiotherapy, can increase the risk of development or progression of atherosclerosis. To elucidate the effects of radiation on atherosclerosis, we propose a mathematical model to describe radiation-promoted plaque development. This model distinguishes itself from other models by combining plaque initiation and plaque growth, and by incorporating information from biological experiments. It is based on two consecutive processes: a probabilistic dose-dependent plaque initiation process, followed by deterministic plaque growth. As a proof of principle, experimental plaque size data from carotid arteries from irradiated ApoE\(^{{-/-}}\) mice was used to illustrate how this model can provide insight into the underlying biological processes. This analysis supports the promoting role for radiation in plaque initiation, but the model can easily be extended to include dose-related effects on plaque growth if available experimental data would point in that direction. Moreover, the model could assist in designing future biological experiments on this research topic. Additional biological data such as plaque size data from chronically-irradiated mice or experimental data sets with a larger variety in biological parameters can help to further unravel the influence of radiation on plaque development. To the authors’ knowledge, this is the first biophysical model that combines probabilistic and mechanistic modeling which uses experimental data to investigate the influence of radiation on plaque development.     

Biology and philosophy in Yellowstone

Yellowstone National Park poses critical issues in biology and philosophy. Among these are (1) how to value nature, especially at the ecosystem level, and whether to let nature take its course or employ hands-on scientific management; (2) the meaning of natural as this operates in park policy; (3) establishing biological claims on th scale of regional systems; (4) the interplay of natural and cultural history, involving both native and European Americans; (5) and sociopolitical forces as determinants in biological discovery. Alston Chase's strident Playing God in Yellowstone is critized and used as a test of David Hull's naturalistic philosophy of biology. Biology and philosophy in Yellowstone ought to combine for an appropriate environmental ethic.The author thanks Donald A. Crosby, Jann Benson, Tom Wolf, William W. Dunmire, Norman A. Bishop, and Paul Schullery for critical help.     

Do cells in a reproductive state exhibit a fermi-pasta-ulam-fröhlich resonance and emit electromagnetic radiation?

Cells in the reproductive state seem to act like small signal generators and emit radiation which is detectable by small polarizable particles nearby in a medium of suitable osmolarity, but very low conductivity. Evidence for this was seen upon using mouse sarcoma (ascites) cells, and by comparing rapidly dividing mouse "L" fibroblasts with confluent ones. Reproducing cells attracted many more highly polarizable BaTiO₃ particles than they did of the much less polarizable BaSO₄ (dielectric constants 4000 and 11, respectively).This preferential attraction of certain cells for highly polarizable small particles is interpreted as due in large measure to the action of dielectrophoresis on a very small scale.evoked by the presence of nonuniform electric fields of cellular origin acting upon the nearby neutral, polarizable particles.a process called microdielectrophoresis. Consideration of the conductive nature of the surrounding medium forces the conclusion that the cell-generated fields must be oscillatory in nature and have a frequency in the order of a megaherz. These observations recall predictions made earlier by Szent-Györgyi on cellular electronic processes, and by Fröhlich on the possibility of Bose-Einstein condensations to a single quantum state of oscillatory ferroelectric character, due to cooperative long-range interactions among dipolar features of cells. The persistence of oscillatory energy in the lower modes is reminiscent of the Fermi-Pasta-Ulam problem.     

Mathematical Modelling of the Interaction Between Cancer Cells and an Oncolytic Virus: Insights into the Effects of Treatment Protocols

Oncolytic virotherapy is an experimental cancer treatment that uses genetically engineered viruses to target and kill cancer cells. One major limitation of this treatment is that virus particles are rapidly cleared by the immune system, preventing them from arriving at the tumour site. To improve virus survival and infectivity Kim et al. (Biomaterials 32(9):2314–2326, 2011) modified virus particles with the polymer polyethylene glycol (PEG) and the monoclonal antibody herceptin. Whilst PEG modification appeared to improve plasma retention and initial infectivity, it also increased the virus particle arrival time. We derive a mathematical model that describes the interaction between tumour cells and an oncolytic virus. We tune our model to represent the experimental data by Kim et al. (2011) and obtain optimised parameters. Our model provides a platform from which predictions may be made about the response of cancer growth to other treatment protocols beyond those in the experiments. Through model simulations, we find that the treatment protocol affects the outcome dramatically. We quantify the effects of dosage strategy as a function of tumour cell replication and tumour carrying capacity on the outcome of oncolytic virotherapy as a treatment. The relative significance of the modification of the virus and the crucial role it plays in optimising treatment efficacy are explored.     

Use of radionuclides in the study of contaminant cycling processes

Of all the geochemical boundaries, the sediment-water interface an exert the greatest control on the cycling of many elements in shallow aquatic environments such as lakes, rivers, estuaries and coastal embayments and, to a lesser extent in the deep sea. Across this interface, the gradients in physical properties (i.e. density), in chemical conditions (i.e. pH, pE, ligand concentrations), biota abundance (i.e. fauna and flora living near the interface) are large, thus producing potentially large fluxes. Some of the physical, chemical, biological and sedimentary controls operating at or near these interfaces can be deciphered from the measurements of natural radioisotopes (e.g. U/Th series or cosmic-ray produced), bomb fallout isotopes or, most recently, fallout from the Chernobyl-reactor accident. Commercially available, reactor-produced isotopes are most often used in enclosures to elucidate the coupling of the various processes at the sediment-water interface, while the former are used both as geochronological tools in the sediments and as tracers to measure or calibrate the rates of exchange across this interface of nutrients or trace elements associated with water or particles.Applications of radioisotopes for studying biological, physical, chemical and sedimentary processes near the sediment-water interface are discussed. In particular, multitracer approaches to study the dynamic coupling of physical, chemical and biological transport processes in lakes are emphasized. Examples from two hard-water lakes in Switzerland, Lake Biel and Lake Zürich, give evidence for the resuspension of fine (rebound) particles, radionuclides and trace metals from the horizontal boundaries focussing them to their final repositories in the interior of the lake.