An Upper Limit on Nickel Overabundance in the Supercritical Accretion Disk Wind of SS 433 from X-ray Spectroscopy

We analyze a long (with a total exposure time of 120 ks) X-ray observation of the unique Galactic microquasar SS 433 carried out by the XMM-Newton space observatory with the goal of searching for the fluorescent line of neutral (or weakly ionized) nickel at energy 7.5 keV. We consider two models for the formation of fluorescent lines in the spectrum of SS 433: (1) through the reflection of radiation from a putative central X-ray source off the optically thick neutral gas of the supercritical disk "funnel" walls; and (2) due to the scattering of the radiation coming from the hottest parts of the jets in the optically thin wind of the system. We show that for these two cases the flux of the Ni I K-alpha fluorescent line is expected to be 0.45 of the flux of the Fe I K-alpha fluorescent line at 6.4 keV for the relative nickel overabundance Z (Ni)/Z = 10 observed in the jets of SS 433. For the continuum model without the absorption edge of neutral iron, we have found an upper limit on the flux of the narrow Ni I K-alpha fluorescent line of 0.9 x 10(-5) phot s(-1) cm(-2) (90% confidence level). In the continuum model with the absorption edge we have determined an upper limit on the flux of the Ni I K-alpha line at the level of 2.5x10(-5) phot s(-1) cm(-2). At the same time, the flux of the fluorescent iron line has been measured to be 9.9 (8.4) (11.2) x 10(-5) phot s(-1) cm(-2). This result implies that the nickel overabundance in the accretion disk wind should be at least a factor of 1.5 times smal than the corresponding nickel overabundance observed in the jets of SS 433

Some pioneers of European human genetics

Some of the pioneers of human genetics across Europe are described, based on a series of 100 recorded interviews made by the author. These interviews, and the memories of earlier workers in the field recalled by interviewees, provide a vivid picture, albeit incomplete, of the early years of human and medical genetics. From small beginnings in the immediate post-World War 2 years, human genetics grew rapidly across many European countries, a powerful factor being the development of human cytogenetics, stimulated by concerns over the risks of radiation exposure. Medical applications soon followed, with the recognition of human chromosome abnormalities, the need for genetic counselling, the possibility of prenatal diagnosis and later, the applications of human molecular genetics. The evolution of the field has been strongly influenced by the characters and interests of the relatively small number of founding workers in different European countries, as well as by wider social, medical and scientific factors in the individual countries

Human genetics in troubled times and places

Abstract The development of human genetics world-wide during the twentieth century, especially across Europe, has occurred against a background of repeated catastrophes, including two world wars and the ideological problems and repression posed by Nazism and Communism. The published scientific literature gives few hints of these problems and there is a danger that they will be forgotten. The First World War was largely indiscriminate in its carnage, but World War 2 and the preceding years of fascism were associated with widespread migration, especially of Jewish workers expelled from Germany, and of their children, a number of whom would become major contributors to the post-war generation of human and medical geneticists in Britain and America. In Germany itself, eminent geneticists were also involved in the abuses carried out in the name of ‘eugenics’ and ‘race biology’. However, geneticists in America, Britain and the rest of Europe were largely responsible for the ideological foundations of these abuses. In the Soviet Union, geneticists and genetics itself became the object of persecution from the 1930s till as late as the mid 1960s, with an almost complete destruction of the field during this time; this extended also to Eastern Europe and China as part of the influence of Russian communism. Most recently, at the end of the twentieth century, China saw a renewal of government sponsored eugenics programmes, now mostly discarded. During the post-world war 2 decades, human genetics research benefited greatly from recognition of the genetic dangers posed by exposure to radiation, following the atomic bomb explosions in Japan, atmospheric testing and successive accidental nuclear disasters in Russia. Documenting and remembering these traumatic events, now largely forgotten among younger workers, is essential if we are to fully understand the history of human genetics and avoid the repetition of similar disasters in the future. The power of modern human genetic and genomic techniques now gives a greater potential for abuse as well as for beneficial use than has ever been seen in the past

SRG/ART-XC discovery of SRGA J204318.2+443815: Towards the complete population of faint X-ray pulsars

We report the discovery of the new long-period X-ray pulsar SRGA J204318.2+443815/SRGe J204319.0+443820 in a Be binary system. The source was found in the second all-sky survey by the Mikhail Pavlinsky ART-XC telescope on board the SRG mission. The followup observations with XMM-Newton, NICER, and NuSTAR allowed us to discover a strong coherent signal in the source light curve with a period of ~742 s. The pulsed fraction was found to depend on an increase in energy from ~20% in soft X-rays to >50% at high energies, as is typical for X-ray pulsars. The source has a quite hard spectrum with an exponential cutoff at high energies and a bolometric luminosity of Lx ≃ 4 x 1035 erg s-1. The X-ray position of the source is found to be consistent with the optical transient ZTF18abjpmzf, located at a distance of ~8.0 kpc. Dedicated optical and infrared observations with the RTT-150, NOT, Keck, and Palomar telescopes revealed a number of emission lines (Hα, He I, and the Paschen and Braket series) with a strongly absorbed continuum. According to the SRG scans and archival XMM-Newton data, the source flux is moderately variable (by a factor of 4-10) on timescales of several months and years. All this suggests that SRGA J204318.2+443815/SRGe J204319.0+443820 is a new quasipersistent low-luminosity X-ray pulsar in a distant binary system with a Be-star of the B0-B2e class. Thus the SRG observatory allowed us to unveil a hidden population of faint objects, including a population of slowly rotating X-ray pulsars in Be systems.</p

Impaired Inflammatory Responses in Murine Lrrk2-Knockdown Brain Microglia

LRRK2, a Parkinson's disease associated gene, is highly expressed in microglia in addition to neurons; however, its function in microglia has not been evaluated. Using Lrrk2 knockdown (Lrrk2-KD) murine microglia prepared by lentiviral-mediated transfer of Lrrk2-specific small inhibitory hairpin RNA (shRNA), we found that Lrrk2 deficiency attenuated lipopolysaccharide (LPS)-induced mRNA and/or protein expression of inducible nitric oxide synthase, TNF-α, IL-1β and IL-6. LPS-induced phosphorylation of p38 mitogen-activated protein kinase and stimulation of NF-κB-responsive luciferase reporter activity was also decreased in Lrrk2-KD cells. Interestingly, the decrease in NF-κB transcriptional activity measured by luciferase assays appeared to reflect increased binding of the inhibitory NF-κB homodimer, p50/p50, to DNA. In LPS-responsive HEK293T cells, overexpression of the human LRRK2 pathologic, kinase-active mutant G2019S increased basal and LPS-induced levels of phosphorylated p38 and JNK, whereas wild-type and other pathologic (R1441C and G2385R) or artificial kinase-dead (D1994A) LRRK2 mutants either enhanced or did not change basal and LPS-induced p38 and JNK phosphorylation levels. However, wild-type LRRK2 and all LRRK2 mutant variants equally enhanced NF-κB transcriptional activity. Taken together, these results suggest that LRRK2 is a positive regulator of inflammation in murine microglia, and LRRK2 mutations may alter the microenvironment of the brain to favor neuroinflammation

Neuron-glial Interactions

Although lagging behind classical computational neuroscience, theoretical and computational approaches are beginning to emerge to characterize different aspects of neuron-glial interactions. This chapter aims to provide essential knowledge on neuron-glial interactions in the mammalian brain, leveraging on computational studies that focus on structure (anatomy) and function (physiology) of such interactions in the healthy brain. Although our understanding of the need of neuron-glial interactions in the brain is still at its infancy, being mostly based on predictions that await for experimental validation, simple general modeling arguments borrowed from control theory are introduced to support the importance of including such interactions in traditional neuron-based modeling paradigms.Junior Leader Fellowship Program by “la Caixa” Banking Foundation (LCF/BQ/LI18/11630006

Neuron-Glial Interactions

Although lagging behind classical computational neuroscience, theoretical and computational approaches are beginning to emerge to characterize different aspects of neuron-glial interactions. This chapter aims to provide essential knowledge on neuron-glial interactions in the mammalian brain, leveraging on computational studies that focus on structure (anatomy) and function (physiology) of such interactions in the healthy brain. Although our understanding of the need of neuron-glial interactions in the brain is still at its infancy, being mostly based on predictions that await for experimental validation, simple general modeling arguments borrowed from control theory are introduced to support the importance of including such interactions in traditional neuron-based modeling paradigms.Comment: 43 pages, 2 figures, 1 table. Accepted for publication in the "Encyclopedia of Computational Neuroscience," D. Jaeger and R. Jung eds., Springer-Verlag New York, 2020 (2nd edition