POWER LINES AS LOCAL AREA NETWORKS FOR MEASURING AND CONTROL SIGNAL TRANSMISSION

Electrical power distribution networks represent the most attractive medium for digital communication purposes due to an ever increasing demand for environmental management of buildings, security monitoring, office automation or remote control of customer appliances and remote meter reading. Power lines are, however, heavily stressed with interference from various sources. Both interference and attenuation are time-variant and frequency-selective in an arbitrary way. The prospective user has to overcome the impairments with a severely restricted level of transmission power, e.g. 5 mW in Germany; the transmission bandwidth, however, exceeds 100 kHz. Obviously simple and inexpensive modulation schemes for digital data transmission such as amplitude shift keying (ASK) or frequency shift keying (FSK) are ruled out. A significant success of band-spreading techniques has been demonstrated by several field trials and extended measurements at different power line networks. Application of spread spectrum techniques generally involves high effort; this is especially true for frequency hopping, which proved advantageous in practical applications. Exploiting the possibilities of modern microelectronics, including design and production of ASICs, recently led to a break-through. A five-year research project based on frequency hopping spread spectrum signaling opened up power lines as local area networks e.g. for office automation or remote meter reading. Transmitter and receiver prototypes were constructed for evaluation of the proposed ideas at various power line networks. Transmitters are based on standard microcontrollers, whereas an application specific integrated circuit (ASIC) with a complexity of about ·5000 gates is the heart of the receiver. Due to completely digital signal processing. the prototypes are useful as a base for series production

The role of L1 use for L1 attrition

While the factor ‘language contact’ is often named among the most important for the development of individual language attrition, empirical validations of this claim are few and far between. This contribution argues that a bilingual’s use of the first language comprises very diverse situations which cannot be subsumed under one predictor variable. Grosjean’s (2001) framework of language modes is invoked as a useful way of structuring the use of the L1 by immigrants. A statistical investigation of these different types of L1 use on the one hand and language proficiency data on the other demonstrates that the impact of both active and passive exposure to the first language on attrition is anything but straightforward

New upper bounds for the density of translative packings of three-dimensional convex bodies with tetrahedral symmetry

In this paper we determine new upper bounds for the maximal density of translative packings of superballs in three dimensions (unit balls for the $l_3^p$-norm) and of Platonic and Archimedean solids having tetrahedral symmetry. These bounds give strong indications that some of the lattice packings of superballs found in 2009 by Jiao, Stillinger, and Torquato are indeed optimal among all translative packings. We improve Zong's recent upper bound for the maximal density of translative packings of regular tetrahedra from $0.3840\ldots$ to $0.3745\ldots$, getting closer to the best known lower bound of $0.3673\ldots$. We apply the linear programming bound of Cohn and Elkies which originally was designed for the classical problem of packings of round spheres. The proofs of our new upper bounds are computational and rigorous. Our main technical contribution is the use of invariant theory of pseudo-reflection groups in polynomial optimization

Mitochondrial reactive oxygen species drive proinflammatory cytokine production

Recent work indicates that mitochondrial ROS act via several pathways to elicit proinflammatory cytokines in human and mouse cells

Malarial Hemozoin Is a Nalp3 Inflammasome Activating Danger Signal

BACKGROUND: Characteristic symptoms of malaria include recurrent fever attacks and neurodegeneration, signs that are also found in patients with a hyperactive Nalp3 inflammasome. Plasmodium species produce a crystal called hemozoin that is generated by detoxification of heme after hemoglobin degradation in infected red blood cells. Thus, we hypothesized that hemozoin could activate the Nalp3 inflammasome, due to its particulate nature reminiscent of other inflammasome-activating agents. METHODOLOGY/PRINCIPAL FINDINGS: We found that hemozoin acts as a proinflammatory danger signal that activates the Nalp3 inflammasome, causing the release of IL-1beta. Similar to other Nalp3-activating particles, hemozoin activity is blocked by inhibiting phagocytosis, K(+) efflux and NADPH oxidase. In vivo, intraperitoneal injection of hemozoin results in acute peritonitis, which is impaired in Nalp3-, caspase-1- and IL-1R-deficient mice. Likewise, the pathogenesis of cerebral malaria is dampened in Nalp3-deficient mice infected with Plasmodium berghei sporozoites, while parasitemia remains unchanged. SIGNIFICANCE/CONCLUSIONS: The potent pro-inflammatory effect of hemozoin through inflammasome activation may possibly be implicated in plasmodium-associated pathologies such as cerebral malaria

Malarial Hemozoin Is a Nalp3 Inflammasome Activating Danger Signal

BACKGROUND: Characteristic symptoms of malaria include recurrent fever attacks and neurodegeneration, signs that are also found in patients with a hyperactive Nalp3 inflammasome. Plasmodium species produce a crystal called hemozoin that is generated by detoxification of heme after hemoglobin degradation in infected red blood cells. Thus, we hypothesized that hemozoin could activate the Nalp3 inflammasome, due to its particulate nature reminiscent of other inflammasome-activating agents. METHODOLOGY/PRINCIPAL FINDINGS: We found that hemozoin acts as a proinflammatory danger signal that activates the Nalp3 inflammasome, causing the release of IL-1beta. Similar to other Nalp3-activating particles, hemozoin activity is blocked by inhibiting phagocytosis, K(+) efflux and NADPH oxidase. In vivo, intraperitoneal injection of hemozoin results in acute peritonitis, which is impaired in Nalp3-, caspase-1- and IL-1R-deficient mice. Likewise, the pathogenesis of cerebral malaria is dampened in Nalp3-deficient mice infected with Plasmodium berghei sporozoites, while parasitemia remains unchanged. SIGNIFICANCE/CONCLUSIONS: The potent pro-inflammatory effect of hemozoin through inflammasome activation may possibly be implicated in plasmodium-associated pathologies such as cerebral malaria

Inflammasome and IL-1β-Mediated Disorders

The NLRP3 inflammasome is an intracellular complex that regulates the release of proinflammatory cytokines such as interleukin-1β in response to exogenous pathogens and endogenous danger signals. Evidence from studies involving human genetics, human ex vivo mononuclear cell responses, and in vivo and in vitro murine models confirms the importance of the inflammasome and interleukin-1β in the pathogenesis of several inherited and complex diseases. The availability of several effective interleukin-1β targeted therapies has allowed for successful proof-of-concept studies in several of these disorders. However, many other diseases are likely to be mediated by the inflammasome and interleukin-1β, providing additional targets in the future

Glyburide inhibits the Cryopyrin/Nalp3 inflammasome

Glyburide, a sulfonylurea drug commonly used to treat type 2 diabetes, shuts down IL-1β secretion by preventing Cyropyrin activation

Particle length-dependent titanium dioxide nanomaterials toxicity and bioactivity

<p>Abstract</p> <p>Background</p> <p>Titanium dioxide (TiO₂) nanomaterials have considerable beneficial uses as photocatalysts and solar cells. It has been established for many years that pigment-grade TiO₂(200 nm sphere) is relatively inert when internalized into a biological model system (in vivo or in vitro). For this reason, TiO₂nanomaterials are considered an attractive alternative in applications where biological exposures will occur. Unfortunately, metal oxides on the nanoscale (one dimension < 100 nm) may or may not exhibit the same toxic potential as the original material. A further complicating issue is the effect of modifying or engineering of the nanomaterial to be structurally and geometrically different from the original material.</p> <p>Results</p> <p>TiO₂nanospheres, short (< 5 μm) and long (> 15 μm) nanobelts were synthesized, characterized and tested for biological activity using primary murine alveolar macrophages and in vivo in mice. This study demonstrates that alteration of anatase TiO₂nanomaterial into a fibre structure of greater than 15 μm creates a highly toxic particle and initiates an inflammatory response by alveolar macrophages. These fibre-shaped nanomaterials induced inflammasome activation and release of inflammatory cytokines through a cathepsin B-mediated mechanism. Consequently, long TiO₂nanobelts interact with lung macrophages in a manner very similar to asbestos or silica.</p> <p>Conclusions</p> <p>These observations suggest that any modification of a nanomaterial, resulting in a wire, fibre, belt or tube, be tested for pathogenic potential. As this study demonstrates, toxicity and pathogenic potential change dramatically as the shape of the material is altered into one that a phagocytic cell has difficulty processing, resulting in lysosomal disruption.</p