Cross-Modulation of Homeostatic Responses to Temperature,Oxygen and Carbon Dioxide in C. elegans

Different interoceptive systems must be integrated to ensure that multiple homeostatic insults evoke appropriate behavioral and physiological responses. Little is known about how this is achieved. Using C. elegans, we dissect cross-modulation between systems that monitor temperature, O₂ and CO₂. CO₂ is less aversive to animals acclimated to 15°C than those grown at 22°C. This difference requires the AFD neurons, which respond to both temperature and CO₂ changes. CO₂ evokes distinct AFD Ca²⁺ responses in animals acclimated at 15°C or 22°C. Mutants defective in synaptic transmission can reprogram AFD CO₂ responses according to temperature experience, suggesting reprogramming occurs cell autonomously. AFD is exquisitely sensitive to CO₂. Surprisingly, gradients of 0.01% CO₂/second evoke very different Ca²⁺ responses from gradients of 0.04% CO₂/second. Ambient O₂ provides further contextual modulation of CO₂ avoidance. At 21% O₂ tonic signalling from the O₂-sensing neuron URX inhibits CO₂ avoidance. This inhibition can be graded according to O₂ levels. In a natural wild isolate, a switch from 21% to 19% O₂ is sufficient to convert CO₂ from a neutral to an aversive cue. This sharp tuning is conferred partly by the neuroglobin GLB-5. The modulatory effects of O₂ on CO₂ avoidance involve the RIA interneurons, which are post-synaptic to URX and exhibit CO₂-evoked Ca²⁺ responses. Ambient O₂ and acclimation temperature act combinatorially to modulate CO₂ responsiveness. Our work highlights the integrated architecture of homeostatic responses in C. elegans.     

Slow growth improves compensation ability: examining growth rate and starvation endurance in pit-building antlions from semi-arid and hyper-arid regions

Different environments are expected to exert differential selective pressures, often generating distinct sets of traits in organisms inhabiting different geographic regions. Starvation endurance is an important trait for organisms in harsh (i.e., extreme climate and/or biotically poor) and unpredictable environments. This is especially true for sit-and-wait predators, such as antlions, which experience stronger fluctuations in prey arrivals than do actively searching predators. We conducted an experimental comparison of starvation endurance in pit-building antlions, originating from semi-arid and hyper-arid environments. We hypothesized that individuals from the climatically harsher and biotically poor environment (i.e., hyper-arid) should be better adapted to endure long starvation periods. Additionally, we posited that faster-growing individuals are expected to be more sensitive to starvation because of their need to sustain higher metabolic rates. We found that antlions originating from the semi-arid region maintained higher activity levels, which led to slightly higher mass loss rates during starvation, but enabled faster recovery when food supply was renewed. Conversely, antlions originating from the hyper-arid region had lower activity levels, consistent with their lower rate of mass loss during starvation, but this came at the expense of decreased response to prey and lower growth rate when food became available again. Each strategy holds its advantages for coping with long starvation periods, and we cannot say decisively which strategy is better. Results from both regions were consistent with the predictions of the growth compensation phenomenon: antlions that were fed less frequently pre-starvation grew at faster rates when food supply was renewed. Our study demonstrates that individuals originating from different environments adopt different strategies in order to endure starvation, exemplifying antlions’ ability to compensate for mass lost during starvation.     

Haemoplasmas in wild rodents: Routes of transmission and infection dynamics

The way that some parasites and pathogens persist in the hostile environment of their host for long periods remains to be resolved. Here, longitudinal field surveys were combined with laboratory experiments to investigate the routes of transmission and infection dynamics of such a pathogen—a wild rodent haemotropic bacterium, specifically a Mycoplasma haemomuris‐like bacterium. Fleaborne transmission, direct rodent‐to‐rodent transmission and vertical transmission from fleas or rodents to their offspring were experimentally quantified, and indications were found that the main route of bacterial transmission is direct, although its rate of successful transmission is low (~20%). The bacterium's temporal dynamics was then compared in the field to that observed under a controlled infection experiment in field‐infected and laboratory‐infected rodents, and indications were found, under all conditions, that the bacterium reached its peak infection level after 25–45 days and then decreased to low bacterial loads, which persist for the rodent's lifetime. These findings suggest that the bacterium relies on persistency with low bacterial loads for long‐term coexistence with its rodent host, having both conceptual and applied implications.     

Nutrition and behavioral management of bottle-raised moose calves

The exceedingly high mortality rates generally associated with artificially raising neonatal moose frequently can be attributed to improper nutritional management and poor husbandry techniques. Dietary-induced diarrhea caused by inappropriate milk replacers is common in moose calves raised in captivity. To avoid diarrhea, calves are often purposefully underfed, resulting in poor growth rates during the first 4 weeks when maternally raised calves rely on milk as their sole energy source. We developed a milk formula and feeding protocol modeled after milk composition and neonatal intake rates measured in maternally raised moose calves. Growth rates for bottle-raised calves during the first 30 days (752 g/day) were similar to maternally raised calves and at least twice that of most previously published bottle-raising efforts. No diet-induced gastrointestinal disorders were encountered, and all calves were successfully weaned and survived their first year. Zoo Biol 16:495–503, 1997. © 1997 Wiley-Liss, Inc.     

Discovery of a hepatitis C target and its pharmacological inhibitors by microfluidic affinity analysis

More effective therapies are urgently needed against hepatitis C virus (HCV), a major cause of viral hepatitis. We used in vitro protein expression and microfluidic affinity analysis to study RNA binding by the HCV transmembrane protein NS4B, which plays an essential role in HCV RNA replication. We show that HCV NS4B binds RNA and that this binding is specific for the 3' terminus of the negative strand of the viral genome with a dissociation constant (Kd) of approximately 3.4 nM. A high-throughput microfluidic screen of a compound library identified 18 compounds that substantially inhibited binding of RNA by NS4B. One of these compounds, clemizole hydrochloride, was found to inhibit HCV RNA replication in cell culture that was mediated by its suppression of NS4B's RNA binding, with little toxicity for the host cell. These results yield new insight into the HCV life cycle and provide a candidate compound for pharmaceutical development.     

The Cardiocoil stent-artery interaction

An analytical approach for the mechanical interaction of the self-expanding Cardiocoil stent with the stenosed artery is presented. The damage factor as the contact stress at the stent-artery interface is determined. The stent is considered as an elastic helical rod having a nonlinear pressure-displacement dependence, while the artery is modeled by an elastic cylindrical shell. An influence of a moderate relative thickness of the shell is estimated. The equations for both the stent and the artery are presented in the stent-associated helical coordinates. The computational efficiency of the model enabled to carry out a parametric study of the damage factor. Comparative examinations are conducted for the stents made of the helical rods with circular and rectangular cross sections. It was found, in particular, that, under same other conditions, the damage factor for the stent with a circular cross section may be two times larger than that for a rectangular one.     

Device thrombogenicity emulation: a novel method for optimizing mechanical circulatory support device thromboresistance

Mechanical circulatory support (MCS) devices provide both short and long term hemodynamic support for advanced heart failure patients. Unfortunately these devices remain plagued by thromboembolic complications associated with chronic platelet activation--mandating complex, lifelong anticoagulation therapy. To address the unmet need for enhancing the thromboresistance of these devices to extend their long term use, we developed a universal predictive methodology entitled Device Thrombogenicity Emulation (DTE) that facilitates optimizing the thrombogenic performance of any MCS device--ideally to a level that may obviate the need for mandatory anticoagulation. DTE combines in silico numerical simulations with in vitro measurements by correlating device hemodynamics with platelet activity coagulation markers--before and after iterative design modifications aimed at achieving optimized thrombogenic performance. DTE proof-of-concept is demonstrated by comparing two rotary Left Ventricular Assist Devices (LVADs) (DeBakey vs HeartAssist 5, Micromed Houston, TX), the latter a version of the former following optimization of geometrical features implicated in device thrombogenicity. Cumulative stresses that may drive platelets beyond their activation threshold were calculated along multiple flow trajectories and collapsed into probability density functions (PDFs) representing the device 'thrombogenic footprint', indicating significantly reduced thrombogenicity for the optimized design. Platelet activity measurements performed in the actual pump prototypes operating under clinical conditions in circulation flow loops--before and after the optimization with the DTE methodology, show an order of magnitude lower platelet activity rate for the optimized device. The robust capability of this predictive technology--demonstrated here for attaining safe and cost-effective pre-clinical MCS thrombo-optimization--indicates its potential for reducing device thrombogenicity to a level that may significantly limit the extent of concomitant antithrombotic pharmacotherapy needed for safe clinical device use.     

A 20-Gene Set Predictive of Progression to Severe Dengue

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Why is melanoma so metastatic?

Malignant melanoma is one of the most aggressive cancers and can disseminate from a relatively small primary tumor and metastasize to multiple sites, including the lung, liver, brain, bone, and lymph nodes. Elucidating the molecular and genetic changes that take place during the metastatic process has led to a better understanding of why melanoma is so metastatic. Herein, we describe the unique features that distinguish melanoma from other solid tumors and contribute to the malignant phenotype of melanoma cells. For example, although melanoma cells are highly antigenic, they are extremely efficient at evading host immune response. Melanoma cells share numerous cell surface molecules with vascular cells, are highly angiogenic, are mesenchymal in nature, and possess a higher degree of ‘stemness’ than do other solid tumors. Finally, analysis of melanoma mutations has revealed that the gene expression profile of malignant melanoma is different from that of other cancers. Elucidating these molecular and genetic processes in highly metastatic melanoma can lead to the development of improved treatment and individualized therapy options.