137 research outputs found
ESCRTs regulate amyloid precursor protein sorting in multivesicular bodies and intracellular amyloid-β accumulation.
Intracellular amyloid-β (Aβ) accumulation is a key feature of early Alzheimer's disease and precedes the appearance of Aβ in extracellular plaques. Aβ is generated through proteolytic processing of amyloid precursor protein (APP), but the intracellular site of Aβ production is unclear. APP has been localized to multivesicular bodies (MVBs) where sorting of APP onto intraluminal vesicles (ILVs) could promote amyloidogenic processing, or reduce Aβ production or accumulation by sorting APP and processing products to lysosomes for degradation. Here, we show that APP localizes to the ILVs of a subset of MVBs that also traffic EGF receptor (EGFR), and that it is delivered to lysosomes for degradation. Depletion of the endosomal sorting complexes required for transport (ESCRT) components, Hrs (also known as Hgs) or Tsg101, inhibited targeting of APP to ILVs and the subsequent delivery to lysosomes, and led to increased intracellular Aβ accumulation. This was accompanied by dramatically decreased Aβ secretion. Thus, the early ESCRT machinery has a dual role in limiting intracellular Aβ accumulation through targeting of APP and processing products to the lysosome for degradation, and promoting Aβ secretion
Aβ accumulation causes MVB enlargement and is modelled by dominant negative VPS4A.
BACKGROUND: Alzheimer's disease (AD)-linked β-amyloid (Aβ) accumulates in multivesicular bodies (MVBs) with the onset of AD pathogenesis. Alterations in endosomes are among the earliest changes associated with AD but the mechanism(s) that cause endosome enlargement and the effects of MVB dysfunction on Aβ accumulation and tau pathology are incompletely understood. METHODS: MVB size and Aβ fibrils in primary neurons were visualized by electron microscopy and confocal fluorescent microscopy. MVB-dysfunction, modelled by expression of dominant negative VPS4A (dnVPS4A), was analysed by biochemical methods and exosome isolation. RESULTS: Here we show that AD transgenic neurons have enlarged MVBs compared to wild type neurons. Uptake of exogenous Aβ also leads to enlarged MVBs in wild type neurons and generates fibril-like structures in endocytic vesicles. With time fibrillar oligomers/fibrils can extend out of the endocytic vesicles and are eventually detectable extracellularly. Further, endosomal sorting complexes required for transport (ESCRT) components were found associated with amyloid plaques in AD transgenic mice. The phenotypes previously reported in AD transgenic neurons, with net increased intracellular levels and reduced secretion of Aβ, were mimicked by blocking recycling of ESCRT-III by dnVPS4A. DnVPS4A further resembled AD pathology by increasing tau phosphorylation at serine 396 and increasing markers of autophagy. CONCLUSIONS: We demonstrate that Aβ leads to MVB enlargement and that amyloid fibres can form within the endocytic pathway of neurons. These results are consistent with the scenario of the endosome-lysosome system representing the site of initiation of Aβ aggregation. In turn, a dominant negative form of the CHMP2B-interacting protein VPS4A, which alters MVBs, leads to accumulation and aggregation of Aβ as well as tau phosphorylation, mimicking the cellular changes in AD
APP depletion alters selective pre- and post-synaptic proteins
The normal role of Alzheimer's disease (AD)-linked amyloid precursor protein (APP) in the brain remains incompletely understood. Previous studies have reported that lack of APP has detrimental effects on spines and electrophysiological parameters. APP has been described to be important in synaptic pruning during development. The effect of APP knockout on mature synapses is complicated by this role in development. We previously reported on differential changes in synaptic proteins and receptors in APP mutant AD transgenic compared to wild-type neurons, which revealed selective decreases in levels of pre- and post-synaptic proteins, including of surface glutamate receptors. In the present study, we undertook a similar analysis of synaptic composition but now in APP knockout compared to wild-type mouse neurons. Here we demonstrate alterations in levels of selective pre- and post-synaptic proteins and receptors in APP knockout compared to wild-type mouse primary neurons in culture and brains of mice in youth and adulthood. Remarkably, we demonstrate selective increases in levels of synaptic proteins, such as GluA1, in neurons with APP knockout and with RNAi knockdown, which tended to be opposite to the reductions seen in AD transgenic APP mutant compared to wild-type neurons. These data reinforce that APP is important for the normal composition of synapses
Putting the self in self-correction: findings from the loss-of-confidence project
Science is often perceived to be a self-correcting enterprise. In principle, the assessment of scientific claims is supposed to proceed in a cumulative fashion, with the reigning theories of the day progressively approximating truth more accurately over time. In practice, however, cumulative self-correction tends to proceed less efficiently than one might naively suppose. Far from evaluating new evidence dispassionately and infallibly, individual scientists often cling stubbornly to prior findings. Here we explore the dynamics of scientific self-correction at an individual rather than collective level. In 13 written statements, researchers from diverse branches of psychology share why and how they have lost confidence in one of their own published findings. We qualitatively characterize these disclosures and explore their implications. A cross-disciplinary survey suggests that such loss-of-confidence sentiments are surprisingly common among members of the broader scientific population yet rarely become part of the public record. We argue that removing barriers to self-correction at the individual level is imperative if the scientific community as a whole is to achieve the ideal of efficient self-correction
IMPROVING CYANOBACTERIA AND CYANOTOXIN MONITORING IN SURFACE WATERS FOR DRINKING WATER SUPPLY
GEWEX water vapor assessment (G-VAP): final report
Este es un informe dentro del Programa para la Investigación del Clima Mundial (World Climate Research Programme, WCRP) cuya misión es facilitar el análisis y la predicción de la variabilidad de la Tierra para proporcionar un valor añadido a la sociedad a nivel práctica. La WCRP tiene varios proyectos centrales, de los cuales el de Intercambio Global de Energía y Agua (Global Energy and Water Exchanges, GEWEX) es uno de ellos. Este proyecto se centra en estudiar el ciclo hidrológico global y regional, así como sus interacciones a través de la radiación y energía y sus implicaciones en el cambio global. Dentro de GEWEX existe el proyecto de Evaluación del Vapor de Agua (VAP, Water Vapour Assessment) que estudia las medidas de concentraciones de vapor de agua en la atmósfera, sus interacciones radiativas y su repercusión en el cambio climático global.El vapor de agua es, de largo, el gas invernadero más importante que reside en la atmósfera. Es, potencialmente, la causa principal de la amplificación del efecto invernadero causado por emisiones de origen humano (principalmente el CO2). Las medidas precisas de su concentración en la atmósfera son determinantes para cuantificar este efecto de retroalimentación positivo al cambio climático. Actualmente, se está lejos de tener medidas de concentraciones de vapor de agua suficientemente precisas para sacar conclusiones significativas de dicho efecto. El informe del WCRP titulado "GEWEX water vapor assessment. Final Report" detalla el estado actual de las medidas de las concentraciones de vapor de agua en la atmósfera. AEMET ha colaborado en la generación de este informe y tiene a unos de sus miembros, Xavier Calbet, como co-autor de este informe
Creating and maintaining play connection in a toddler peer group
This study explores how one and two year old peers (henceforth toddlers) participate in joint play activities in a natural group-care setting. We focus on joint play activity between three toddler peers during one full day-care day in a Finnish toddler classroom. Questions guiding the analysis concern the sequential understanding of how play emerges within peer interaction and how toddler peers are able to build sustained co-participation in their joint play during the day. The analysis showed that joint play was fragmented and organized in short segments of dyadic or triadic interaction. Re-establishments of joint play and accumulation of significant play signals during the day were important practices for toddlers to constitute social organization and sustained co-participation in their multi-party peer play. The results strengthen our understanding of very young children as both more and less competent play companions in their peer groups and guide adults’ practice in relation to peer play in toddler classrooms.Peer reviewe
Three-dimensional kinematic motion analysis of a daily activity drinking from a glass: a pilot study
BACKGROUND: Development of reliable and objective evaluation methods is required, particularly for natural and goal-oriented upper-extremity tasks. Three-dimensional imaging measurement techniques have turned out to be a powerful tool for a quantitative and qualitative assessment of multijoint movements. The purpose of this study was to develop and test a method of three-dimensional motion analysis for the activity "drinking from a glass" and describe the drinking task with kinematic variables in control subjects. METHODS: A protocol was developed for the drinking activity including the set-up of cameras and positions of the markers and the subject. The drinking task included reaching, forward transport with glass, drinking, back transport and returning the hand to the initial position. An optoelectronic system was used for the three-dimensional kinematic motion capture. Movement times, velocities, joint angles and interjoint coordination for shoulder and elbow were computed and analyzed for twenty control subjects. Test-retest consistency was evaluated for six subjects. RESULTS: The test protocol showed good consistency in test-retest. Phase definitions for the drinking task were defined and verified. Descriptive kinematic variables were obtained for movement times, positions, velocities and joint angles for shoulder and elbow joint. Interjoint coordination between shoulder and elbow joint in reaching phase showed a high correlation. CONCLUSION: This study provides a detailed description of the three-dimensional kinematic analysis of the drinking task. Our approach to investigate and analyze a goal-oriented daily activity has a great clinical potential. Consequently, the next step is to use and test this protocol on persons with impairments and disabilities from upper extremities
Contribution of nitrogen fixation to the external nitrogen load of a water quality control reservoir (Kis-Balaton Water Protection System, Hungary)
Comparison of techniques used to count single-celled viable phytoplankton
Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Springer for personal use, not for redistribution. The definitive version was published in Journal of Applied Phycology 24 (2012): 751-758, doi:10.1007/s10811-011-9694-z.Four methods commonly used to count phytoplankton were evaluated based upon the precision of concentration
estimates: Sedgewick Rafter and membrane filter direct counts, flow cytometry, and flow-based imaging cytometry
(FlowCAM). Counting methods were all able to estimate the cell concentrations, categorize cells into size classes,
and determine cell viability using fluorescent probes. These criteria are essential to determine whether discharged
ballast water complies with international standards that limit the concentration of viable planktonic organisms based
on size class. Samples containing unknown concentrations of live and UV-inactivated phytoflagellates (Tetraselmis
impellucida) were formulated to have low concentrations (<100 ml-1) of viable phytoplankton. All count methods
used chlorophyll a fluorescence to detect cells and SYTOX fluorescence to detect non-viable cells. With the
exception of one sample, the methods generated live and non-viable cell counts that were significantly different
from each other, although estimates were generally within 100% of the ensemble mean of all subsamples from all
methods. Overall, percent coefficient of variation (CV) among sample replicates was lowest in membrane filtration
sample replicates, and CVs for all four counting methods were usually lower than 30% (although instances of ~60%
were observed). Since all four methods were generally appropriate for monitoring discharged ballast water,
ancillary considerations (e.g., ease of analysis, sample processing rate, sample size, etc.) become critical factors for
choosing the optimal phytoplankton counting method.This study was supported by the U.S. Coast Guard Research and Development Center under contract HSCG32-07-
X-R00018. Partial research support to DMA and DMK was provided
through NSF International Contract 03/06/394, and Environmental Protection Agency Grant RD-83382801-0
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