2 kirja Karl Morgensternile, Moskau

http://tartu.ester.ee/record=b1784409~S1*es

2 kirja Karl Morgensternile, Moskwa

http://tartu.ester.ee/record=b1814151~S1*es

Baff Mediates Survival of Peripheral Immature B Lymphocytes

B cell maturation is a very selective process that requires finely tuned differentiation and survival signals. B cell activation factor from the TNF family (BAFF) is a TNF family member that binds to B cells and potentiates B cell receptor (BCR)-mediated proliferation. A role for BAFF in B cell survival was suggested by the observation of reduced peripheral B cell numbers in mice treated with reagents blocking BAFF, and high Bcl-2 levels detected in B cells from BAFF transgenic (Tg) mice. We tested in vitro the survival effect of BAFF on lymphocytes derived from primary and secondary lymphoid organs. BAFF induced survival of a subset of splenic immature B cells, referred to as transitional type 2 (T2) B cells. BAFF treatment allowed T2 B cells to survive and differentiate into mature B cells in response to signals through the BCR. The T2 and the marginal zone (MZ) B cell compartments were particularly enlarged in BAFF Tg mice. Immature transitional B cells are targets for negative selection, a feature thought to promote self-tolerance. These findings support a model in which excessive BAFF-mediated survival of peripheral immature B cells contributes to the emergence and maturation of autoreactive B cells, skewed towards the MZ compartment. This work provides new clues on mechanisms regulating B cell maturation and tolerance

Loadings of dissolved organic matter and nutrients from the Neva River into the Gulf of Finland - Biogeochemical composition and spatial distribution within the salinity gradient

We studied the loadings of dissolved organic matter (DOM) and nutrients from the Neva River into the Eastern Gulf of Finland, as well as their distribution within the salinity gradient. Concentrations of dissolved organic carbon (DOC) ranged from 390 to 840 mu M, and were related to absorption of colored DOM (CDOM) at 350 nm, a(CDOM)(350), ranging from 2.70 to 17.8 m(-1). With increasing salinity both DOC and a(CDOM) decreased, whereas the slope of a(CDOM) spectra, S-CDOM(300-700), ranging from 14.3 to 21.2 mu m(-1), increased with salinity. Deviations of these properties from conservative mixing models were occasionally observed within the salinity range of approximately 1-4, corresponding to the region between 27 and 29 degrees E. These patterns are suggested to mostly reflect seasonal changes in properties of river end-member and hydrodynamics of the estuary, rather than non-conservative processes. On the other hand, observed nonlinear relationships observed between a(CDOM)*(350) and S-CDOM(275-295) emphasized the importance of photochemistry among various transformation processes of DOM. Dissolved inorganic nitrogen was effectively transformed in the estuary into particulate organic nitrogen (PON) and dissolved organic nitrogen (DON), of which DON was mostly exported from the estuary, enhancing productivity in nitrogen limited parts of the Gulf of Finland. DON concentrations ranged from 12.4 to 23.5 mu M and its estuarine dynamics were clearly uncoupled from DOC. In contrast to DOC, estuarine DON dynamics suggest that its production exceeds losses in the estuary. Total nitrogen (TN) and phosphorus (TP) loadings from the Neva River and St. Petersburg were estimated as 73.5 Gg N yr(-1) and 4.2 Gg P yr(-1), respectively. Approximately 59% of TN and 53% of TP loads were in organic forms. DOC and DON loadings were estimated as 741.4 Gg C yr(-1) and 19.0 Gg N yr(-1), respectively. Our estimate for DOC loading was evaluated against a previously published carbon budget of the Baltic Sea. According to the updated model, the Baltic Sea could be identified as a weak source of carbon into the atmosphere. (C) 2016 The Authors. Published by Elsevier B.V.Peer reviewe

The 8200 year B.P. event in the slope water system, western subpolar North Atlantic

Author Posting. © American Geophysical Union, 2005. This article is posted here by permission of American Geophysical Union for personal use, not for redistribution. The definitive version was published in Paleoceanography 20 (2005): PA2003, doi:10.1029/2004PA001074.Stable isotope, trace metal, alkenone paleothermometry, and radiocarbon methods have been applied to sediment cores in the western subpolar North Atlantic between Hudson Strait and Cape Hatteras to reveal the history of climate in that region over the past ∼11 kyr. We focus on cores from the Laurentian Fan, which is known to have rapid and continuous accumulation of hemipelagic sediment. Although results among our various proxy data are not always in agreement, the weight of the evidence (alkenone sea surface temperature (SST), δ18O and abundance of Globigerinoides ruber) indicates a continual cooling of surface waters over Laurentian Fan, from about 18°C in the early Holocene to about 8°C today. Alternatively, Mg/Ca data on planktonic foraminifera indicate no systematic change in Holocene SST. The inferred long-term decrease in SST was probably driven by decreasing seasonality of Northern Hemisphere insolation. Two series of proxy data show the gradual cooling was interrupted by a two-step cold pulse that began 8500 years ago, and lasted about 700 years. Although this event is associated with the final deglaciation of Hudson Bay, there is no δ18O minimum anywhere in the Labrador Sea, yet there is some evidence for it as far south as Cape Hatteras. Finally, although the 8200 year B.P. event has been implicated in decreasing North Atlantic ventilation, and hence widespread temperature depression on land and at sea, we find inconsistent evidence for a change at that time in deep ocean nutrient content at ∼4 km water depth.Funding for JPS was from the NOAA Climate and Global Change Program (NA 16GP2679), NSF-Earth System History (0116940), the Jeptha H. and Emily V. Wade Award for Research, and a Henry L. and Grace Doherty Professorship. LDK and YR were funded by NSF grant OCE-0117149

Copeptin for risk stratification in non-traumatic headache in the emergency setting: a prospective multicenter observational cohort study

In the emergency setting, non-traumatic headache is a benign symptom in 80% of cases, but serious underlying conditions need to be ruled out. Copeptin improves risk stratification in several acute diseases. Herein, we investigated the value of copeptin to discriminate between serious secondary headache and benign headache forms in the emergency setting.; Patients presenting with acute non-traumatic headache were prospectively enrolled into an observational cohort study. Copeptin was measured upon presentation to the emergency department. Primary endpoint was serious secondary headache defined by a neurologic cause requiring immediate treatment of the underlying disease. Secondary endpoint was the combination of mortality and hospitalization within 3 months. Two board-certified neurologist blinded to copeptin levels verified the endpoints after a structured 3-month-telephone interview.; Of the 391 patients included, 75 (19%) had a serious secondary headache. Copeptin was associated with serious secondary headache (OR 2.03, 95%CI 1.52-2.70, p < 0.0001). Area under the curve (AUC) for copeptin to identify the primary endpoint was 0.70 (0.63-0.76). After adjusting for age > 50, focal-neurological abnormalities, and thunderclap onset of symptoms, copeptin remained an independent predictive factor for serious secondary headache (OR 1.74, 95%CI 1.26-2.39, p = 0.001). Moreover, copeptin improved the AUC of the multivariate logistic clinical model (p-LR-test < 0.001). Even though copeptin values were higher in patients reaching the secondary endpoint, this association was not significant in multivariate logistic regression.; Copeptin was independently associated with serious secondary headache as compared to benign headaches forms. Copeptin may be a promising novel blood biomarker that should be further validated to rule out serious secondary headache in the emergency department.; Study Registration on 08/02/2010 as NCT01174901 at clinicaltrials.gov

The primary headaches: genetics, epigenetics and a behavioural genetic model

The primary headaches, migraine with (MA) and without aura (MO) and cluster headache, all carry a substantial genetic liability. Familial hemiplegic migraine (FHM), an autosomal dominant mendelian disorder classified as a subtype of MA, is due to mutations in genes encoding neural channel subunits. MA/MO are considered multifactorial genetic disorders, and FHM has been proposed as a model for migraine aetiology. However, a review of the genetic studies suggests that the FHM genes are not involved in the typical migraines and that FHM should be considered as a syndromic migraine rather than a subtype of MA. Adopting the concept of syndromic migraine could be useful in understanding migraine pathogenesis. We hypothesise that epigenetic mechanisms play an important role in headache pathogenesis. A behavioural model is proposed, whereby the primary headaches are construed as behaviours, not symptoms, evolutionarily conserved for their adaptive value and engendered out of a genetic repertoire by a network of pattern generators present in the brain and signalling homeostatic imbalance. This behavioural model could be incorporated into migraine genetic research

Effect of remote ischaemic conditioning on clinical outcomes in patients with acute myocardial infarction (CONDI-2/ERIC-PPCI): a single-blind randomised controlled trial.

BACKGROUND: Remote ischaemic conditioning with transient ischaemia and reperfusion applied to the arm has been shown to reduce myocardial infarct size in patients with ST-elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PPCI). We investigated whether remote ischaemic conditioning could reduce the incidence of cardiac death and hospitalisation for heart failure at 12 months. METHODS: We did an international investigator-initiated, prospective, single-blind, randomised controlled trial (CONDI-2/ERIC-PPCI) at 33 centres across the UK, Denmark, Spain, and Serbia. Patients (age >18 years) with suspected STEMI and who were eligible for PPCI were randomly allocated (1:1, stratified by centre with a permuted block method) to receive standard treatment (including a sham simulated remote ischaemic conditioning intervention at UK sites only) or remote ischaemic conditioning treatment (intermittent ischaemia and reperfusion applied to the arm through four cycles of 5-min inflation and 5-min deflation of an automated cuff device) before PPCI. Investigators responsible for data collection and outcome assessment were masked to treatment allocation. The primary combined endpoint was cardiac death or hospitalisation for heart failure at 12 months in the intention-to-treat population. This trial is registered with ClinicalTrials.gov (NCT02342522) and is completed. FINDINGS: Between Nov 6, 2013, and March 31, 2018, 5401 patients were randomly allocated to either the control group (n=2701) or the remote ischaemic conditioning group (n=2700). After exclusion of patients upon hospital arrival or loss to follow-up, 2569 patients in the control group and 2546 in the intervention group were included in the intention-to-treat analysis. At 12 months post-PPCI, the Kaplan-Meier-estimated frequencies of cardiac death or hospitalisation for heart failure (the primary endpoint) were 220 (8·6%) patients in the control group and 239 (9·4%) in the remote ischaemic conditioning group (hazard ratio 1·10 [95% CI 0·91-1·32], p=0·32 for intervention versus control). No important unexpected adverse events or side effects of remote ischaemic conditioning were observed. INTERPRETATION: Remote ischaemic conditioning does not improve clinical outcomes (cardiac death or hospitalisation for heart failure) at 12 months in patients with STEMI undergoing PPCI. FUNDING: British Heart Foundation, University College London Hospitals/University College London Biomedical Research Centre, Danish Innovation Foundation, Novo Nordisk Foundation, TrygFonden

Tabvlae anatomicae Qvas Ad Illvstrandam Hvmani Corporis Fabricam : 1/2, Tabularum anatomicarum Vol.I. Tab. I-XC; Tabularum anatomicarum Vol. II. Tab. XCI-CLXXXII

Elektronische Reproduktion von: Tabvlae anatomicae Qvas Ad Illvstrandam Hvmani Corporis Fabricam / Collegit Et Cvravit Ivstvs Christianvs Loder : 1/2, Tabularum anatomicarum Vol.I. Tab. I-XC; Tabularum anatomicarum Vol. II. Tab. XCI-CLXXXII. - Vimariae : Landes-Industrie-Comptoir, 1803. - [5] Bl., 47, 21, 94, 92, 162, 66, 24, 168 S., [25] Bl. - Standort: Universität Marburg, Universitätsbibliothek. - Signatur: 085 2 2022/00136. - Bemerkungen: Provenienz: Bünger, Christian Heinrich (1782-1842). Digitalisiert 202