Variants of hemoglobin F and observations on hemoglobin F (Malta)

The major hemoglobin component found in the blood of humans at birth is fetal hemoglobin, hemoglobin F. In common with most other human hemoglobins it has a tetrameric structure, each molecule being made up of two different pairs of polypeptide chains. At birth hemoglobin F accounts for 60-80% of the hemoglobin present in the blood. Hemoglobin F-Malta is the most recent variant discovered and is of special interest to Malta as it is only here that it has been reported (Cauchi et aI., 1969). Hemoglobin F-Malta is unique among the fetal variants in that it has a very high incidence, being present at birth in the blood of one Maltese child in every fifty. The variant disappears as the baby matures, in common with other fetal hemoglobin variants, and has not been observed in any parents. Infants born with hemoglobin F-Malta are apparently healthy and have no other hematological anomalies. The results of an ongoing study on the relative rates of disappearance of the hemoglobins F-Malta and F as the infants mature are displayed. Because of the high incidence of hemoglobin F-Malta it is possible to carry out a much more comprehensive study on the relative rates of disappearance than it is in the case of other fetal variants.peer-reviewe

Enrichment of innate lymphoid cell populations in gingival tissue

Innate lymphoid cells (ILCs) are a population of lymphocytes that act as the first line of immunologic defense at mucosal surfaces. The ILC family in the skin, lungs, and gastrointestinal tissues has been investigated, and there are reports of individual subsets of ILCs in the oral tissues. We sought to investigate the whole ILC population (group 1, 2, and 3 subsets) in the murine gingivae and the lymph nodes draining the oral cavity. We show that ILCs made up a greater proportion of the whole CD45+ lymphocyte population in the murine gingivae (0.356% ± 0.039%) as compared with the proportion of ILCs in the draining lymph nodes (0.158% ± 0.005%). Cytokine profiling of the ILC populations demonstrated different proportions of ILC subsets in the murine gingivae versus the regional lymph nodes. The majority of ILCs in the draining lymph nodes expressed IL-5, whereas there were equal proportions of IFN-γ- and IL-5 expressing ILCs in the oral mucosa. The percentage of IL-17+ ILCs was comparable between the murine gingivae and the oral draining lymph nodes. These data suggest an enrichment of ILCs in the murine gingivae, and these ILCs reflect a cytokine profile discrepant to that of the local draining lymph nodes. These studies indicate diversity and enrichment of ILCs at the oral mucosal surface. The function of ILCs in the oral cavity remains to be determined; here, we provide a premise of ILC populations that merits future consideration in investigations of mouse models and human tissues

Correction to:Easy as (Happiness) Pie? A Critical Evaluation of a Popular Model of the Determinants of Well-Being (Journal of Happiness Studies, (2020), 21, 4, (1285-1301), 10.1007/s10902-019-00128-4)

In the original publication, the text (line 10) under the heading “3 Re‑examining the Numerical Estimates of the Effect of Genes and Circumstances” with sub heading “3.1 How Much Variance in Chronic Happiness Levels can be Explained by Genetic Factors?” has been published incorrectly

Easy as (Happiness) Pie? A Critical Evaluation of a Popular Model of the Determinants of Well-Being

An underlying principle behind much of the research in positive psychology is that individuals have considerable leeway to increase their levels of happiness. In an influential article that is frequently cited in support of such claims, Lyubomirsky et al. (Rev Gen Psychol 9:111–131, 2005. https://doi.org/10.1037/1089-2680.9.2.111) put forward a model (subsequently popularized under the name of the “happiness pie”) in which approximately 50% of individual differences in happiness are due to genetic factors and 10% to life circumstances, leaving 40% available to be changed via volitional activities. We re-examined Lyubomirsky et al.’s claims and found several apparent deficiencies in their chain of arguments on both the empirical and the conceptual level. We conclude that there is little empirical evidence for the variance decomposition suggested by the “happiness pie,” and that even if it were valid, it is not necessarily informative with respect to the question of whether individuals can truly exert substantial influence over their own chronic happiness level. We believe that our critical re-examination of Lyubomirsky et al.’s seminal article offers insights into some common misconceptions and pitfalls of scientific inference, and we hope that it might contribute to the construction of a more rigorous and solid empirical basis for the field of positive psychology

Electrochemical Study of Biotin-Modified Self-Assembled Monolayers: Recommendations for Robust Preparation

The development of the underpinning methodology for the production of robust, well-formed, and densely packed biotin-HPDP functionalised gold surfaces, the crucial first step in immobilising bimolecules on surfaces, is described. Self-assembled monolayers (SAMs) with biotin end-groups were prepared on polycrystalline gold surfaces according to a published method. The layers formed were studied using cyclic voltammetry to determine the composition of the layer and its quality. Crystal impedance spectroscopy was also applied as a complimentary indicator of the composition of the layer.For the first time, the effect of assembly time on the properties of the layer was studied along with the composition of the layer and the ability of the precursor molecule to self-assemble by oxidative addition

Factors affecting amninolaevulinic acid-induced generation of protoporphyrin IX

Photodynamic therapy (PDT) may cause tumour cell destruction by direct toxicity or by inducing cellular hypoxia as a result of microcirculatory shutdown. Aminolaevulinic acid (ALA) causes cellular accumulation of protoporphyrin IX (PPIX) in cells exposed to it in excess. PPIX can be used as a photosensitizer for PDT. Microcirculatory shutdown may be induced by toxicity to the endothelial and vascular smooth muscle (VSM) cells or by release of vasoactive substances. We have studied whether PPIX is produced by endothelial, VSM and tumour cells on exposure to ALA and whether these cell lines are directly damaged by PDT in vitro. Tumour endothelial cells are angiogenic and we have, therefore, investigated the effect of cellular proliferation rates on PPIX generation. Tumour cells generate more PPIX intracellularly than the non-neoplastic cell lines studied and are correspondingly more sensitive to PDT-induced cytotoxicity. Endothelial cells are sensitive to PDT-induced cytotoxicity and accumulate between 1.5 and four times more PPIX when proliferating (as during tumour-induced angiogenesis) than when quiescent. We conclude that PPIX-mediated PDT may exert some of its effects on the microcirculation of treated tissues by direct toxicity to endothelial and VSM cells, and that this toxicity may be enhanced in the tumour microenvironment

On some problems involving Hardy's function

Some problems involving the classical Hardy function $$Z(t) := \zeta(1/2+it)\bigl(\chi(1/2+it)\bigr)^{-1/2}, \quad \zeta(s) = \chi(s)\zeta(1-s)$$ are discussed. In particular we discuss the odd moments of $Z(t)$, the distribution of its positive and negative values and the primitive of $Z(t)$. Some analogous problems for the mean square of $|\zeta(1/2+it)|$ are also discussed.Comment: 15 page

The reactions and ashes of thermonuclear explosions on neutron stars

This paper reports on the detailed rp-process reaction flow on an accreting neutron star and the resulting ashes of a type I X-ray burst. It is obtained by coupling a 298 isotope reaction network to a self-consistent one-dimensional model calculation with a constant accretion rate of dM/dt=1.0e17g/s (0.09 Eddington).Comment: 4 pages, 2 figures, submitted to the INPC2004 proceeding