Introduction: An increasing number of patients present with multiple symptoms affecting many organs including the brain due to multiple mediators released by mast cells. These unique tissue immune cells are critical for allergic reactions triggered by immunoglobulin E (IgE), but are also stimulated (not activated) by immune, drug, environmental, food, infectious, and stress triggers, leading to secretion of multiple mediators often without histamine and tryptase. The presentation, diagnosis, and management of the spectrum of mast cell disorders are very confusing. As a result, neuropsychiatric symptoms have been left out, and diagnostic criteria made stricter excluding most patients.
Areas covered: A literature search was performed on papers published between January 1990 and November 2018 using MEDLINE. Terms used were activation, antihistamines, atopy, autism, brain fog, heparin, KIT mutation, IgE, inflammation, IL-6, IL-31, IL-37, luteolin, mast cells, mastocytosis, mediators, mycotoxins, release, secretion, tetramethoxyluteolin, and tryptase.
Expert opinion: Conditions associated with elevated serum or urine levels of any mast cell mediator, in the absence of comorbidities that could explain elevated levels, should be considered ‘Mast Cell Mediator Disorders (MCMD).’ Emphasis should be placed on the identification of unique mast cell mediators, and development of drugs or supplements that inhibit their release. 相似文献
To investigate whether exercise- and ultrasonic "fog"-induced asthma are due to the same mechanism, i.e. mediator release induced by osmotic changes, we measured the serum neutrophil chemotactic activity before and after exercise and inhalation of "fog" in 15 asthmatic subjects. To assess changes in airway caliber we measured specific airway conductance (SGaw); to assess changes in neutrophil chemotactic activity we measured the maximum distance reached by neutrophils in a filter when challenged with the subject's serum in a Boyden chamber. In 10 subjects, SGaw decreased by more than 35% and neutrophil chemotactic activity increased significantly (P less than 0.05) both after exercise and "fog", whereas in five subjects no change occurred either after exercise or "fog". We conclude that both exercise- and "fog"-induced asthma are associated with increased serum neutrophil chemotactic activity, and that both stimuli may cause asthma by osmotically triggering mediator release from mast cells. 相似文献
The diurnal and seasonal water cycles in the Amazon remain poorly simulated in general circulation models, exhibiting peak evapotranspiration in the wrong season and rain too early in the day. We show that those biases are not present in cloud-resolving simulations with parameterized large-scale circulation. The difference is attributed to the representation of the morning fog layer, and to more accurate characterization of convection and its coupling with large-scale circulation. The morning fog layer, present in the wet season but absent in the dry season, dramatically increases cloud albedo, which reduces evapotranspiration through its modulation of the surface energy budget. These results highlight the importance of the coupling between the energy and hydrological cycles and the key role of cloud albedo feedback for climates over tropical continents.Tropical forests, and the Amazon in particular, are the biggest terrestrial CO2 sinks on the planet, accounting for about 30% of the total net primary productivity in terrestrial ecosystems. Hence, the climate of the Amazon is of particular importance for the fate of global CO2 concentration in the atmosphere (1). Besides the difficulty of estimating carbon pools (1–3), our incapacity to correctly predict CO2 fluxes in the continental tropics largely results from inaccurate simulation of the tropical climate (1, 2, 4, 5). More frequent and more intense droughts in particular are expected to affect the future health of the Amazon and its capacity to act as a major carbon sink (6–8). The land surface is not isolated, however, but interacts with the weather and climate through a series of land−atmosphere feedback loops, which couple the energy, carbon, and water cycles through stomata regulation and boundary layer mediation (9).Current General Circulation Models (GCMs) fail to correctly represent some of the key features of the Amazon climate. In particular, they (i) underestimate the precipitation in the region (10, 11), (ii) do not reproduce the seasonality of either precipitation (10, 11) or surface fluxes such as evapotranspiration (12), and (iii) produce errors in the diurnal cycle and intensity of precipitation, with a tendency to rain too little and too early in the day (13, 14). In the more humid Western part of the basin, surface incoming radiation, evapotranspiration, and photosynthesis all tend to peak in the dry season (15–17), whereas GCMs simulate peaks of those fluxes in the wet season (10, 11). Those issues might be related to the representation of convection (1, 2, 4, 5, 13, 14) and vegetation water stress (6–8, 15–17) in GCMs.We here show that we can represent the Amazonian climate using a strategy opposite to GCMs in which we resolve convection and parameterize the large-scale circulation (Methods). The simulations lack many of the biases observed in GCMs and more accurately capture the differences between the dry and wet season of the Amazon in surface heat fluxes and precipitation. Besides top-of-the-atmosphere insolation, the simulations require the monthly mean temperature profile as an input. We demonstrate that this profile, whose seasonal cycle itself is a product of the coupled ocean−land−atmosphere dynamics, mediates the seasonality of the Amazonian climate by modulating the vertical structure of the large-scale circulation in such a way that thermal energy is less effectively ventilated in the rainy season. 相似文献
Microbes are the foundation of marine ecosystems [Falkowski PG, Fenchel T, Delong EF (2008) Science 320(5879):1034–1039]. Until now, the analytical framework for understanding the implications of ocean warming on microbes has not considered thermal exposure during transport in dynamic seascapes, implying that our current view of change for these critical organisms may be inaccurate. Here we show that upper-ocean microbes experience along-trajectory temperature variability up to 10 °C greater than seasonal fluctuations estimated in a static frame, and that this variability depends strongly on location. These findings demonstrate that drift in ocean currents can increase the thermal exposure of microbes and suggests that microbial populations with broad thermal tolerance will survive transport to distant regions of the ocean and invade new habitats. Our findings also suggest that advection has the capacity to influence microbial community assemblies, such that regions with strong currents and large thermal fluctuations select for communities with greatest plasticity and evolvability, and communities with narrow thermal performance are found where ocean currents are weak or along-trajectory temperature variation is low. Given that fluctuating environments select for individual plasticity in microbial lineages, and that physiological plasticity of ancestors can predict the magnitude of evolutionary responses of subsequent generations to environmental change [Schaum CE, Collins S (2014) Proc Biol Soc 281(1793):20141486], our findings suggest that microbial populations in the sub-Antarctic (∼40°S), North Pacific, and North Atlantic will have the most capacity to adapt to contemporary ocean warming.Photosynthetic marine microbes, otherwise known as phytoplankton, underpin all of the production-based ocean ecosystem services, and impact on human health and well-being through their regulation of climate (1), formation of harmful algal blooms (2), and support of biodiversity at multiple dimensions and trophic levels (3). Heterotrophic microbes, including bacteria, Archaea, and eukaryotes, are also critical for ocean functioning, being the dominant remineralizers of organic matter and key players in the Earth’s biogeochemical cycles (1, 4). Depending on the CO2 emissions scenario, the surface ocean is predicted to warm 2–4 °C on average by 2100 (5). Because microbes demonstrate a steep decline in growth at temperatures exceeding their optimum (6–10), such warming has the potential to affect the distribution and diversity of marine microbes through exceedance of thermal limits and changes in fitness, with cascading impacts to ecosystem services (11, 12).However, by virtue of their large population sizes, relatively rapid reproduction, and high diversity, microbes have considerable potential to mitigate negative consequences of past and present ocean change through phenotypic plasticity (acclimation) and adaptive evolution (genetic change). Until now, our understanding of how microbial communities will be reorganized under contemporary ocean change has developed from empirical studies involving examination of the current geographic distribution of microbial taxa and their relationships with temperature and other environmental parameters (8, 10, 13), laboratory investigations that measure performance of microbial ecotypes (thought to be representative of populations) under different conditions (6, 7, 9, 14), and modeling studies that use microbial traits describing resource (e.g., nutrients, light) utilization to estimate fitness and predict future distributions of microbes under projected ocean change (15–17). The limitation of these studies is that microbial traits are assumed to be constant during model runs, so the microbes themselves are not responding to changes in their environment (18). However, there is increasing evidence that photosynthetic microbes are altering their realized niches in response to contemporary changes in ocean temperature and irradiance (19), and that the geographic origin of microbial ecotypes influences their plasticity (capacity for physiological acclimation) (9, 20)—as well as adaptation (21)—at the population level (potentially via increased rate of mitotic mutations) (22), with some ecotypes tolerant of a broad range of temperature and others more thermally specialized (7). Microbes generally experience the ocean as a viscous medium (23), and their motion is therefore predominantly determined by drift with ocean currents (noting that some taxa are motile or regulate their buoyancy) (24). As a result, their habitat temperatures are highly dynamic and cannot be described assuming a fixed location. This means there currently is no clear global estimate of the thermal history of marine microbes, making it difficult to understand their realized thermal niche and relate this to their performance under controlled (typically stable) experimental conditions, let alone predict the impact of a 2–4 °C projected rise in mean ocean temperature.Thus, to advance our understanding of marine microbial acclimation and adaptation, and to determine which microbes can keep pace with rates of contemporary ocean change, a spatially explicit understanding of temperature exposure from the perspective of the moving organism is critical (25). This requires examining the temperature experienced by marine microbes in a Lagrangian (drift) framework. 相似文献