119 research outputs found
Opposing effects of dehydroepiandrosterone and dexamethasone on the generation of monocyte-derived dendritic cells
BACKGROUND: Dehydroepiandrosterone (DHEA) has been suggested as an
immunostimulating steroid hormone, of which the effects on the development
of dendritic cells (DC) are unknown. The effects of DHEA often oppose
those of the other adrenal glucocorticoid, cortisol. Glucocorticoids (GC)
are known to suppress the immune response at different levels and have
recently been shown to modulate the development of DC, thereby influencing
the initiation of the immune response. Variations in the duration of
exposure to, and doses of, GC (particularly dexamethasone (DEX)) however,
have resulted in conflicting effects on DC development. AIM: In this
study, we describe the effects of a continuous high level of exposure to
the adrenal steroid DHEA (10 M) on the generation of immature DC from
monocytes, as well as the effects of the opposing steroid DEX on this
development. RESULTS: The continuous presence of DHEA (10 M) in
GM-CSF/IL-4-induced monocyte-derived DC cultures resulted in immature DC
with a morphology and functional capabilities similar to those of typical
immature DC (T cell stimulation, IL-12/IL-10 production), but with a
slightly altered phenotype of increased CD80 and decreased CD43 expression
(markers of maturity). The continuous presence of DEX at a concentration
of 10 M in the monocyte/DC cultures resulted in the generation of
plastic-adherent macrophage-like cells in place of typical immature DC,
with increased CD14 expression, but decreased expression of the typical DC
markers CD1a, CD40 and CD80. These cells were strongly reactive to acid
phosphatase, but equally capable of stimulating T cell prolifer
Increased level of serum cytokines, chemokines and adipokines in patients with schizophrenia is associated with disease and metabolic syndrome
SummaryAt present there are strong indications of a shared vulnerability factor for schizophrenia (SZ), diabetes and the metabolic syndrome (metS). In this study we focus on an aberrantly activated monocyte/macrophage system as the shared factor.We measured in SZ patients (n=144), the serum levels of monocyte/macrophage cytokines/chemokines/adipokines CCL2, CCL4, IL-1β, TNF-α, IL-6, PTX3, leptin, adiponectin, PAI-1, OPG and ICAM-1 and compared these levels to healthy controls (HC) (n=138). Using multivariate analysis, we studied the effect of the presence of the disease SZ, the components of the metS including BMI, the levels of lipids (HDL cholesterol and triglycerides (TG)), diabetes (hyperglycemia) and the use of antipsychotic medication, on the serum levels of these immune compounds.We found all measured immune compounds with the exception of PAI-1 and OPG to be elevated in the SZ patient population. Multivariate analysis showed that elevations were linked to gender (ICAM-1, leptin, TNF-α and adiponectin), an increased BMI (leptin, adiponectin), hyperglycemia/diabetes (CCL4, and OPG), reduced HDL-cholesterol or increased levels of TG (adiponectin and PTX3) or the metS (CCL2, leptin and adiponectin). IL-1β and IL-6 were the only immune compounds raised in the serum of patients not affected by any of the included factors.Although many of the immune compounds were found linked to (components of) the metS, the most dominant linkage was found with the disease schizophrenia, confirming earlier reports on increased monocyte/macrophage activation as a key component for understanding the pathogenesis of schizophrenia
Duality and asymptotic geometries
We consider a series of duality transformations that leads to a constant
shift in the harmonic functions appearing in the description of a configuration
of branes. This way, for several intersections of branes, we can relate the
original brane configuration which is asymptotically flat to a geometry of the
type adS_k \xx E^l \xx S^m. The implications of our results for supersymmetry
enhancement, M(atrix) theory at finite N, and for supergravity theories in
diverse dimensions are discussed.Comment: 13 pages, Latex, references adde
Copper-Heparin Inhalation Therapy To Repair Emphysema: A Scientific Rationale
Current pharmacotherapy of chronic obstructive pulmonary disease (COPD)
aims at reducing respiratory symptoms and exacerbation frequency. Effective therapies to
reduce disease progression, however, are still lacking. Furthermore, COPD medications
showed less favorable effects in emphysema than in other COPD phenotypes. Elastin fibers
are reduced and disrupted, whereas collagen levels are increased in emphysematous lungs.
Protease/antiprotease imbalance has historically been regarded as the sole cause of emphysema. However, it is nowadays appreciated that emphysema may also be provoked by
perturbations in the sequential repair steps following elastolysis. Essentiality of fibulin-5
and lysyl oxidase-like 1 in the elastin restoration process is discussed, and it is argued that
copper deficiency is a plausible reason for failing elastin repair in emphysema patients.
Since copper-dependent lysyl oxidases crosslink elastin as well as collagen fibers, copper
supplementation stimulates accumulation of both proteins in the extracellular matrix.
Restoration of abnormal elastin fibers in emphysematous lungs is favorable, whereas
stimulating pulmonary fibrosis formation by further increasing collagen concentrations
and organization is detrimental. Heparin inhibits collagen crosslinking while stimulating
elastin repair and might therefore be the ideal companion of copper for emphysema
patients. Efficacy and safety considerations may lead to a preference of pulmonary administration of copper-heparin over systemic administration
Psychological Coping and Behavioral Adjustment Among Older Adults in Times of COVID-19: Exploring the Protective Role of Working Memory and Habit Propensity
The impact of the COVID-19 pandemic on mental health, well-being, and behavior is likely influenced by individual characteristics that determine one’s capacity for resilience. In this exploratory study, we examined whether individual differences in working memory (WM) capacity and habit propensity (HP), measured before the outbreak, could predict variation in subsequent psychological coping efficacy (as operationalized by measures of depression, mental well-being, perceived stress, and loneliness) and behavioral adjustment (by evaluating compliance and self-reported automaticity of four COVID-19 guidelines) among Dutch older adults (n = 36) during the pandemic (measured April 25 to May 6, 2020). While we found elevated levels of depression and emotional loneliness, overall mental well-being, and perceived stress were not affected by the pandemic. Contrary to our expectations, we found no robust evidence for a protective role of WM in predicting these outcomes, although our findings hint at a positive relationship with perceived change in mental well-being. Interestingly, WM and HP were found to affect the self-reported automaticity levels of adherence to behavioral COVID-19 guidelines (i.e., washing hands, physical distancing), where a strong HP appeared beneficial when deliberate resources were less available (e.g., low WM capacity). These novel and preliminary findings offer new potential avenues for investigating individual differences in resilience in times of major life events or challenges
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