Acclimation to temperature is one of the survival strategies used by organisms to adapt to changing environ-mental temperatures. caenorhabditis elegans' cold tolerance is altered by previous cultivation temperatur...
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Acclimation to temperature is one of the survival strategies used by organisms to adapt to changing environ-mental temperatures. caenorhabditis elegans' cold tolerance is altered by previous cultivation temperature, and similarly, past low-temperature induces a longer lifespan. Temperature is thought to cause a large shift in ho-meostasis, lipid metabolism, and reproduction in the organism because it is a direct physiological factor during chemical events. This paper will share and discuss what we know so far about the neural and molecular mechanisms that control cold tolerance and lifespan by altering lipid metabolism and physiological character-istics. We hope that this will contribute to a better understanding of how organisms respond to temperature changes.
Animals' sensory systems adjust their responsiveness to environmental stimuli that vary greatly in their intensity. Here we report the neural mechanism of experience-dependent sensory adjustment, especially gain c...
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Animals' sensory systems adjust their responsiveness to environmental stimuli that vary greatly in their intensity. Here we report the neural mechanism of experience-dependent sensory adjustment, especially gain control, in the ASH nociceptive neurons in caenorhabditis elegans. Using calcium imaging under gradual changes in stimulus intensity, we find that the ASH neurons of naive animals respond to concentration increases in a repulsive odor 2nonanone regardless of the magnitude of the concentration increase. However, after preexposure to the odor, the ASH neurons exhibit significantly weak responses to a small gradual increase in odor concentration while their responses to a large gradual increase remain strong. Thus, preexposure changes the slope of stimulus-response relationships (i.e., gain control). Behavioral analysis suggests that this gain control contributes to the preexposure-dependent enhancement of odor avoidance behavior. Mathematical analysis reveals that the ASH response consists of fast and slow components, and that the fast component is specifically suppressed by preexposure for the gain control. In addition, genetic analysis suggests that G protein signaling may be required for the regulation of fast component. We propose how prior experience dynamically and specifically modulates stimulus-response relationships in sensory neurons, eventually leading to adaptive modulation of behavior.
Manganese oxide based materials are considered as alternate non-noble metal electrocatalysts for oxygen reduction reaction (ORR). These materials possess rich redox chemistry and can decompose hydrogen peroxide dispro...
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Manganese oxide based materials are considered as alternate non-noble metal electrocatalysts for oxygen reduction reaction (ORR). These materials possess rich redox chemistry and can decompose hydrogen peroxide disproportionately to drive the oxygen reduction towards efficient 4-electron pathway. In this work, a set of MnO nanostructures supported on activated charcoal (MnO/c) with varying MnO loadings are prepared by ball milling followed by in-situ pyrolysis. The MnO/ccomposites are tested for ORR activity by employing cyclic voltammetry and linear sweep voltammetry using rotating-ring disk electrode (RRDE) in 0.1 M KOH. The results indicate that the ORR activity as well as catalytic pathways are sensitive to MnO loading. The ORR activities of the composites follow volcano type relationship with the quantity of MnO loadings. The role of MnO loading on surface morphology, hydrophilicity, electrochemical double layer capacitance (c-dl) and electrochemical active surface area (EcSA) of the composites has been investigated and correlated with ORR activity. Among the MnO electroctalysts studied, 18 wt% MnO loaded sample showed the highest activity, close to that of standard Pt/c, with onset potential of 1.02 V vs. RHE and 3.48 mA cm(-2) limiting disk current in RRDE at 0.2 V. This electrocatalyst also preferred 4-electron reduction pathway in ORR and produced least amount of hydrogen peroxide. No hydrophilicity effect is found on the ORR activity of MnO/c electrocatalysts.
Backgroundp24/transmembrane Emp24 domain (TMED) proteins are a set of evolutionarily conserved, single pass transmembrane proteins that have been shown to facilitate protein secretion and selection of cargo proteins t...
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Backgroundp24/transmembrane Emp24 domain (TMED) proteins are a set of evolutionarily conserved, single pass transmembrane proteins that have been shown to facilitate protein secretion and selection of cargo proteins to transport vesicles in the cellular secretion pathway. However, their functions in animal development are incompletely understood. ResultsThe c. elegans genome encodes eight identified TMED genes, with at least one member from each defined subfamily (alpha, beta, gamma, delta). TMED gene mutants exhibit a shared set of defects in embryonic viability, animal movement, and vulval morphology. Two gamma subfamily genes, tmed-1 and tmed-3, exhibit the ability to compensate for each other, as defects in movement and vulva morphology are only apparent in double mutants. TMED mutants also exhibit a delay in breakdown of basement membrane during vulva development. conclusionsThe results establish a genetic and experimental framework for the study of TMED gene function in c. elegans, and argue that a functional protein from each subfamily is important for a shared set of developmental processes. A specific function for TMED genes is to facilitate breakdown of the basement membrane between the somatic gonad and vulval epithelial cells, suggesting a role for TMED proteins in tissue reorganization during animal development.
Metal-organic frameworks (MOFs) constitute a class of crystalline porous materials employed in storage and energy conversion applications. MOFs possess characteristics that render them ideal in the preparation of elec...
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Metal-organic frameworks (MOFs) constitute a class of crystalline porous materials employed in storage and energy conversion applications. MOFs possess characteristics that render them ideal in the preparation of electrocatalysts, and exhibit excellent performance for the hydrogen evolution reaction (HER). Herein, H-Ni/NiO/ccatalysts were synthesized from a Ni-based MOF hollow structure via a two-step process involving carbonization and oxidation. Interestingly, the performance of the H-Ni/NiO/ccatalyst was superior to those of H-Ni/c, H-NiO/c, and NH-Ni/NiO/ccatalysts for the HER. Notably, H-Ni/NiO/c exhibited the best electrocatalytic activity for the HER, with a low overpotential of 87 mV for 10 mA cm(-2) and a Tafel slope of 91.7 mV dec(-1). The high performance is ascribed to the synergistic effect of the metal/metal oxide and hollow architecture, which is favorable for breaking the H-OH bond, forming hydrogen atoms, and enabling charge transport. These results indicate that the employed approach is promising for fabricating cost-effective catalysts for hydrogen production in alkaline media.
Mild inhibition of mitochondrial function leads to longevity. Genetic disruption of mitochondrial respiratory components either by mutation or RNAi greatly extends the lifespan in yeast, worms, and drosophila. This ha...
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Mild inhibition of mitochondrial function leads to longevity. Genetic disruption of mitochondrial respiratory components either by mutation or RNAi greatly extends the lifespan in yeast, worms, and drosophila. This has given rise to the idea that pharmacologically inhibiting mitochondrial function would be a workable strategy for postponing aging. Toward this end, we used a transgenic worm strain that expresses the firefly luciferase enzyme widely to evaluate compounds by tracking real-time ATP levels. We identified chrysin and apigenin, which reduced ATP production and increased the lifespan of worms. Mechanistically, we discovered that chrysin and apigenin transiently inhibit mitochondrial respiration and induce an early ROS, and the lifespan-extending effect is dependent on transient ROS formation. We also show that AAK-2/AMPK, DAF-16/FOXO, and SKN-1/NRF-2 are required for chrysin or apigenin-mediated lifespan extension. Temporary increases in ROS levels trigger an adaptive response in a mitohormetic way, thereby increasing oxidative stress capacity and cellular metabolic adaptation, finally leading to longevity. Thus, chrysin and apigenin represent a class of compounds isolated from natural products that delay senescence and improve age-related diseases by inhibiting mitochondrial function and shed new light on the function of additional plant-derived polyphenols in enhancing health and delaying aging. collectively, this work provides an avenue for pharmacological inhibition of mitochondrial function and the mechanism underlining their lifespan-extending properties.
Many tropical and subtropical plant lineages have independently evolved c4 photosynthesis. The convergent evolution of this complex functional trait from different ancestors is reflected in variations in the structura...
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Many tropical and subtropical plant lineages have independently evolved c4 photosynthesis. The convergent evolution of this complex functional trait from different ancestors is reflected in variations in the structural and biochemical characteristics of c4 components such as enzymes and cellular specializations. The mechanism of c4 carbon concentration mostly involves coordinated function of mesophyll and bundle sheath cells. Important adaptations of the c4 syndrome include increased vein density and the development of photosynthetic bundle sheath cells with low gas conductance. In addition, the enzymes and transporters of the c4 pathway evolved via the co-option of multiple genes, each derived from a specific lineage of isoforms present in nonc4-ancestors. In particular, the adaptation of c4 enzymes resulted in a variety of structural and biochemical modifications, generally leading to increased catalytic efficiency and regulation by metabolites and post-translational modifications. Differences in these adaptations are particularly evident in the c4-acid decarboxylation step, which can be catalyzed by three decarboxylases that define the c4 subtypes. Associated with the biochemical subtypes, there are also differences in the extend of grana staking and localization of bundle sheath cells chloroplasts. The presence of a suberin layer and symplasticconnections also likely vary among the different c4-subtypes. This review examines the current understanding of the diversity of structural and functional changes in key components of the c4 carbon concentration mechanism. This knowledge is necessary not only to identify divergent solutions for convergent optimization of c4 components in different c4 lineages, but also to guide their creation for rational synthetic biology approaches.
Aims Resistance to valproic acid (VPA) is a major challenge for epilepsy treatment. We aimed to explore the mechanism underlying this resistance. Methods Pentylenetetrazol-induced chronic epileptic rats were administe...
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Aims Resistance to valproic acid (VPA) is a major challenge for epilepsy treatment. We aimed to explore the mechanism underlying this resistance. Methods Pentylenetetrazol-induced chronic epileptic rats were administered VPA (250 mg/Kg) for 14 days;rats with controlled seizure stages (seizure score(14th-before) <= 0) and latent time (latent time(14th-before) >= 0) were considered VPA-responsive, while the others were considered nonresponsive. Differentially expressed genes (DEGs) between the VPA-responsive and nonresponsive rat hippocampus transcriptomes were identified, and their functions were evaluated. The roles of postsynaptic density (PSD) and Homer1 were also determined. Furthermore, a subtype of Homer1 (Homer1b/c) was overexpressed or silenced in HT22 cells to determine its effect on VPA efficacy. Moreover, the membrane levels of mGluR1/5 directly bound to Homer1b/c were assessed. Results Overall, 264 DEGs commonly enriched in the PSD between VPA-responsive and nonresponsive rats. Among them, Homer1 was more highly expressed in the hippocampus of nonresponses compared to that of responses. Overexpression of Homer1b/c interrupted VPA efficacy by increasing reactive oxygen species production, lactate dehydrogenase release, and calcium content. Furthermore, it induced the overexpression of mGluR1 and mGluR5. conclusion Overexpression of Homer1b/c influenced VPA efficacy, revealing it could be a target to improve the efficacy of this treatment.
Liposome-mediated delivery is a possible means to overcome several shortcomings with c. elegans as a model for identifying and testing drugs that retard aging. These include confounding interactions between drugs and ...
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Liposome-mediated delivery is a possible means to overcome several shortcomings with c. elegans as a model for identifying and testing drugs that retard aging. These include confounding interactions between drugs and the nematodes' bacterial food source and failure of drugs to be taken up into nematode tissues. To explore this, we have tested liposome-mediated delivery of a range of fluorescent dyes and drugs in c. elegans. Liposome encapsulation led to enhanced effects on lifespan, requiring smaller quantities of compounds, and enhanced uptake of several dyes into the gut lumen. However, one dye (Texas red) did not cross into nematode tissues, showing that liposomes cannot ensure the uptake of all compounds. Of six compounds previously reported to extend lifespan (vitamin c, N-acetylcysteine, glutathione (GSH), trimethadione, thioflavin T (ThT), and rapamycin), this effect was reproduced for the latter four in a condition-dependent manner. For GSH and ThT, antibiotics abrogated life extension, implying a bacterially mediated effect. With GSH, this was attributable to reduced early death from pharyngeal infection and associated with alterations of mitochondrial morphology in a manner suggesting a possible innate immune training effect. By contrast, ThT itself exhibited antibiotic effects. For rapamycin, significant increases in lifespan were only seen when bacterial proliferation was prevented. These results document the utility and limitations of liposome-mediated drug delivery for c. elegans. They also illustrate how nematode-bacteria interactions can determine the effects of compounds on c. elegans lifespan in a variety of ways.
centrioles, together with the surrounding peri-centriolar material (PcM), constitute the centrosome, a major microtubule-organizing center of animal cells. Despite being critical in many cells for signaling, motility ...
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centrioles, together with the surrounding peri-centriolar material (PcM), constitute the centrosome, a major microtubule-organizing center of animal cells. Despite being critical in many cells for signaling, motility and division, centrioles can be eliminated in some systems, including in the vast majority of differentiating cells during embryogenesis in caenorhabditis elegans. Whether the cells retaining centrioles in the resulting L1 larvae do so because they lack an activity that eliminates centrioles in the other cells is not known. Moreover, the extent to which centrioles and PcM remain present in later stages of worm development, when all cells but those of the germ line are terminally differentiated, is not known. Here, by fusing cells that lack centrioles with cells that retain them, we established that L1 larvae do not possess a diffusible elimination activity sufficient to remove centrioles. Moreover, analyzing PcM core proteins in L1 larval cells that retain centrioles, we found that some such proteins, but not all, are present as well. Furthermore, we uncovered that foci of centriolar proteins remain present in specific terminally differentiated cells of adult hermaphrodites and males, in particular in the somatic gonad. correlating the time at which cells were born with the fate of their centrioles revealed that it is not cell age, but instead cell fate, that determines whether and when centrioles are eliminated. Overall, our work maps the localization of centriolar and PcM core proteins in the post-embryonicc. elegans lineage, thereby providing an essential blueprint for uncovering mechanisms modulating their presence and function.
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