Vegetation database of Tatarstan

© 2017 Gebrüder Borntraeger, 70176 Stuttgart, Germany. The Republic of Tatarstan is situated between forest and steppe natural zones in the boreal mega-ecotone and has a high species and plant community diversity. The Vegetation Database of Tatarstan (GIVD Database ID: EU-RU-011) is based on phytosociological relevés, herbaria and floristic records. It includes over 8,000 plot records, almost half of them being georeferenced. The database is part of the European Vegetation Archive (EVA) and sPlot projects. In EVA it has a semi-restricted access mode

Issues of the world economy’s assessment : the demographic factor

The article analyzes the impact of the demographic factor on the prospects for the development of the world economy. The basis of the methodology is an analysis of the dynamics of macro indicators of the world's 10 leading economies, whose contribution exceeds 61% of world GDP. In the article the dynamics of macroeconomic and demographic indicators were analyzed, and their interrelation was established. The study analyzes the dynamics of the world economy. In the course of the study, it was shown that globalization brings not only advantages, but notable threats. The economic growth within the last 21 years led to the accumulation of colossal debts, which in future will become a limitation of the development of the world economy. The article shows that attempts to overcome demographic problems in the last decades did not have any success, and consequently, in the future it will be a barrier to the sustainable development of the world economy.peer-reviewe

Two Late Quaternary Pollen Records from South-Central Alaska

Pollen records from Wonder and Ten Mile lakes, located at aititudinal treeline to the north and south of the Alaska Range respectively, document the vegetation history of a portion of the southern Alaskan boreal forest. The new pollen diagrams indicate a Betula shrub tundra, preceded at Wonder Lake by a sparse herb tundra, which characterized these two areas during latest Wisconsinan times. Populus was in the vicinity of Ten Mile Lake ca. 10,000 BP, but was apparently absent from Wonder Lake. Picea glauca grew at or near Ten Mile Lake by 9100 BP, with P. mariana becoming important ca. 7000 BP. The first forests at Wonder Lake were also dominated by P. glauca and followed by increased numbers of P. mariana. The timing of forest establishment at Wonder Lake is uncertain due to problematic radiocarbon dates. Alnus appears to be common in both regions by ca. 7000 BP. These records suggest that paleo-vegetational reconstructions are more difficult for the southern than northern boreal forests in Alaska because of greater topographic diversity, difficulties with over-representation of some pollen taxa, and problems with radiocarbon dating. Despite these concerns, available data from south-central Alaska suggest that southern and northern forests differ in their vegetational histories. Such differences, when related to temperature fluctuations that have been postulated for the Holocene, imply that the Alaskan boreal forest may not respond uniformly to future global warming.Les inventaires polliniques de Wonder Lake et de Ten Mile Lake, situés à la limite altitudinale des arbres au nord et au sud de la chaîne de l'Alaska permettent de reconstituer l'histoire de la végétation d'une portion de la forêt boréale du sud de l'Alaska. Les nouveaux diagrammes polliniques montrent une toundra arbustive à Betula, précédée au Wonder Lake par une toundra herbacée clairsemée, à la fin du Wisconsinien. Vers 10 000 BP, Populus était dans les environs du Ten Mile Lake, mais était apparamment absent du Wonder Lake. Picea glauca croissait autour du Ten Mile Lake à 9100 BP et P. mariana prenait de l'importance vers 7000 BP. Au Wonder Lake, les premières forêts ont également été dominées par P. glauca, puis par un nombre croissant de P. mariana. La chronologie de !'afforestation est incertaine en raison de datations au radiocarbone douteuses. Alnus semble être une espèce courante dans les deux régions vers 7000 BP. Les inventaires indiquent que la reconstitution de la paléovégétation est plus difficile à faire pour les forêts méridionales que septentrionales de l'Alaska, en raison de la plus grande diversité topographique, la sur-représentation de certains taxons et des problèmes de radio-datation. Les données indiquent tout de même que l'histoire de la végétation des forêts diffèrent au nord et au sud. Ces différences, mises en relation avec les fluctuations de températures présumées de l'Holocène, laissent croire que la forêt de l'Alaska ne répondra pas nécessairement de façon uniforme à un réchauffement climatique éventuel.DbiJibneBbie aiiarpa.viMbi ocaaKOB 03ep Baeae n TeHMaRJi, pacnojioxeHiibix B6JIII3H Bepxiiert rpaiiMUbi Jieca Ha ceBepe H wre A/iflCKiiHCKoro xpeôîa, OTpaacaioT ncropnio pacTHTejibHOCTH KOKIIOH lacr" Sopea/ibHoro jieca AJIBCKH. HoBbie ribiJibuebe anarpaMMbi iiOKaabiBaioT, HTO KycTapmiKOBOfi 6epr30B0fi TyHApe, xapaKTepiioft aJifl 3TMX aByx TeppiiTopufl B Teieime no3iuiero BiicKoiicmia, npemuecTBOBajia B oTaoaceiinnx 03. Banae 6emiaH TpaBHHUCTHa iyHapa. Populus iipopn3parra.n B otcpecruocnix 03. Teii.vianji 10000 /J.H., HO, JlO-BIUHMOMy, OTCyTCTBOBaa B pafione 03. BaHae. 9100 JI.H. B panoHe 03. Tenvianj] H.11I B iienocpeacrBeimoH 6/IH30CTH OT iiero npoH3pacTajia Picea glauca, KOTopan BMepTe c Picea mariana nrpaeT 3Ha'iiiTe/ibnyio pojib B codaBe pacTHTeJibHOCTM OKO/IO 7000 .i.n. B nepBbix Jiecax B paflone 03. BaHae TaKjKe aoMiiiuipoBajia Picea glauca, 110 3aTe,vi pojib Picea mariana iiaHimaeT B03pacacTaTb. Bpe.viH noflB/ieiiHfl jiecoB B panone 03. Banae uoKaiie ycraiiaBJiiiBaeTca iiaaeacHo paaiioyr-jiepoaiibiM McroaoM. Alnus o6pa3yer cooBiuecTBa B06011X pafioiiax OKOJIO 7000 JI.H. nojiyieiuibie aaiiHbie cBiiaeTejibCTByioT 0 TOM, HTO peKoiicTpyKniifl pacTiiTejibiiocTH 6yaer 6ojieecjio>KHon aJin lOîKHbix, ieM aJifl ceaepiibix 6opeajibiibix JiecoB AJIHCKH 1133a SHa'iinejibiioro TonorpafpimecKoro iiecxoacTBa,3aTpyaiieiii!Ji B iiHTepnpeTaumi neKOTopwx nbijibneitbix TaKCOHOB, npoGjieM c paanoyrjiepoaiibiM aaTHpBaiine.M. HeavioTpa tia 3TH npo6jieivibi, nojicpieHHbie aaHiibie noKa3biaiOT, HTO fjopeajibiibie Jieca 11a wre 11 ceBepe ioaciion iacni UetiTajibiion AJIHCKH wweioT pa3Jiiiiyio iiCTopnio. TaKiie pa3Jinmtfl, cBfl3xaiuibie c n3MeiieiijiflMii 3eMJiepaTyp B Teieiuie ro.'ioueiia, cBiiae-Te.TbCTByioT, HTO 6opeajibiibiri Jiec AJIHCKH ,vioxer ne OTBenaTb cienapnio rjio6aJibiioro noTen.ieiina u SyaymeM

Non3 is an essential Drosophila gene required for proper nucleolus assembly

The nucleolus is a dynamic non-membrane-bound nuclear organelle, which plays key roles not only in ribosome biogenesis but also in many other cellular processes. Consistent with its multiple functions, the nucleolus has been implicated in many human diseases, including cancer and degenerative pathologies of the nervous system and heart. Here, we report the characterization of the Drosophila Non3 (Novel nucleolar protein 3) gene, which encodes a protein homologous to the human Brix domain-containing Rpf2 that has been shown to control ribosomal RNA (rRNA) processing. We used imprecise P-element excision to generate four new mutant alleles in the Non3 gene. Complementation and phenotypic analyses showed that these Non3 mutations can be arranged in an allelic series that includes both viable and lethal alleles. The strongest lethal allele (Non3∆600) is a genetically null allele that carries a large deletion of the gene and exhibits early lethality when homozygous. Flies heterozygous for Non3∆600 occasionally exhibit a mild reduction in the bristle size, but develop normally and are fertile. However, heteroallelic combinations of viable Non3 mutations (Non3197, Non3310 and Non3259) display a Minute-like phenotype, consisting in delayed development and short and thin bristles, suggesting that they are defective in ribosome biogenesis. We also demonstrate that the Non3 protein localizes to the nucleolus of larval brain cells and it is required for proper nucleolar localization of Fibrillarin, a protein important for post-translational modification and processing of rRNAs. In summary, we generated a number of genetic and biochemical tools that were exploited for an initial characterization of Non3, and will be instrumental for future functional studies on this gene and its protein product

LYMPH NODE REGULATORY T-CELL IN Muc2-/- MICE WITH HELICOBACTER SPP.

The immune processes associated with the formation of resistance to pathogens in the intestine depend on the microbiome. The maintenance of homeostasis in the intestine is provided by regulatory T-cells. In inflammatory bowel disease (IBD), both a disturbance of the T-regulatory function and changes in microflora are observed. Aggravation of the disease is accompanied by various infections. However, pathobionts such as Helicobacter spp., can affect regulatory T-cells. One of the genetic models for studying IBD is Muc2 knockout mice. In these mice, as in humans with IBD, intestinal epithelial and immune cells closely interact with the microflora. It is believed that the immune cells of the lymph nodes Muc2-/- mice are sensitive to changes in the microflora formed in them. In this study, the effect of Helicobacter spp. on the number and percentage of different types of leukocytes and T regulatory cells in the mesenteric lymph nodes of Muc2-/- mice was studied. The number of CD45+CD19+, CD45+CD3+, CD45+CD3+CD4+, CD45+CD3+CD8+-cells in the mesenteric lymph nodes of Muc2-/- mice was significantly higher to compare with wild-type Muc2+/+ mice. However, the presence of infection in Muc2-/- mice canceled the increase in the number of CD45+CD19+, CD45+CD3+, CD45+CD3+CD4+, CD45+CD3+CD8+-cells. In wild-type Muc2+/+ mice, infection had no significant effect on cells in mesenteric lymph nodes. This change in the decrease in immune cells in the mesenteric lymph nodes under the Helicobacter spp. may be associated with the activation of regulatory T-cells. Indeed, it has been shown that the presence of a congenital Helicobacter spp. infection increased of the number of regulatory T-cells (CD45+CD4+CD25+FoxP3+) in the mesenteric lymph nodes. Well known that regulatory T-cells mediate anti-inflammatory responses in the gut. Thus, an increase in regulatory T-cells promotes a decrease in all types of immune cells in the mesenteric lymph nodes of Muc2-/- mice infected with Helicobacter spp. It could provide an improvement in the vital functions of these mice and possibly reduces inflammatory responses in the intestine. This may indicate that some congenital pathobionts activate of the regulatory mechanisms of immunity and, thereby, have a beneficial effect on the host

In vitro Effects of Biologically Active Vitamin D on Myogenesis: A Systematic Review

Vitamin D (VD) deficiency is associated with muscle weakness. A reduction in the incidence of falls in the elderly following VD supplementation and identification of the VD receptor within muscle cells suggests a direct effect of VD on muscle, but little is known about the underlying mechanisms. Here we systematically searched the literature to identify effects of active VD [1,25(OH)2D3] on skeletal muscle myogenesis in vitro, with no restriction on year of publication. Eligibility was assessed by strict inclusion/exclusion criteria and agreed by two independent investigators. Twelve relevant pa-pers were identified using four different cell types (C2C12, primary mouse satellite cells, primary chick myoblasts, and primary human myoblasts) and a range of myogenic markers (myoD, myogenin, creatine kinase, myosin heavy chain, and myotube size). A clear inhibitory effect of 1,25(OH)2D3 on proliferation was reported, while the effects on the different stages of differentiation were less consistent probably due to variation in cell type, time points and doses of 1,25(OH)2D3 used. However, myotube size was consistently increased by 1,25(OH)2D3. Overall, the evidence suggests that 1,25(OH)2D3 inhibits proliferation and promotes differentiation of myoblasts, but future studies should use time courses to gain a clearer understanding

Role of the Mucin-2 and Kaiso genes in the social behavior of mice

Inflammatory processes in the gut lead to abnormal­ities in various systems of the body, in particular, to changes in the activity of the central nervous system. Although the mechanisms of these effects are not yet known, it has been demonstrated that intestinal inflammation is associated with anxiety and depression. In this work, we used an animal model of intestinal inflammation, which might result in behavioral changes. The animals used were knock-out mice with double mutations in the Kaiso and Mucin-2 genes. The Kaiso gene encodes a transcription factor that is expressed both in the brain and in the intestine. The Mucin-2 gene encodes a protein that serves as a scaffold for the synthesis of intestinal proteoglycan. Mucin-2 is a major proteoglycan of the intestinal mucus layer and performs multiple functions, including barrier and defensive ones. We used knock-out animals with a mutation in the trans­cription factor Kaiso in tests assessing social behavior, but did not observe any difference between test subjects and wild-type animals. By contrast, double knock-out animals that additionally had a mutation in Mucin-2, a major gene for intestinal proteoglycan, displayed significant changes in social behavior: lower aggression rates and higher rates of courtship behavior toward a male intruder. These results suggest that intestinal homeostasis might have a strong impact on the nervous system of the animals. It remains unclear whether the influence of the two genes is synergistic or the knock-out of the Mucin-2 gene alone determines this behavior in mice. Further investigations will help clarify the matter

Sirtuins and chemokines as markers of replicative and induced senescence of human endotheliocytes

Background. One of the factors of the pathogenesis of atherosclerosis and other cardiovascular diseases is induced endothelial senescence. In this regard, the urgent task of molecular biology and medicine is the search for molecules that affect the process of vascular endotheliocytes senescence.The aim. To assess the expression of Sirt-1,3,6 and chemokines IL-4, CXCL11 in the replicative and induced senescence of human endotheliocytes.Materials and methods. The study was conducted on the primary culture of isolated human umbilical vein endothelial cells (HUVECs). HUVECs were cultured under conditions of replicative (natural) and lipopolysaccharide induced senescence.Results. The synthesis of Sirt-1,3,6, IL-4 and CXCL11 was evaluated using western blot analysis. We revealed a decrease in Sirt-1,3,6 synthesis by 1.6–1.8 times (р < 0.05) in the conditions of HUVEC replicative senescence. Induced senescence of endotheliocytes is characterized by a more pronounced decrease (1.7–3.4 times; р < 0.05) in the Sirt-1,3,6 synthesis. CXCL11 synthesis increases by 1.4 times (р < 0.05) in replicative and by 3.4 times (р < 0.05) in induced HUVEC senescence. IL-4 synthesis increases by 4.7 times in conditions of induced HUVEC senescence and doesn’t have changes in replicative senescence of endotheliocytes.Conclusion. These data obtained indicate that sirtuins and chemokines play an important role in the development of endothelial dysfunction observed in natural and induced senescence

Role of intestinal mucin-2 in the effectiveness of the treatment of Helicobacter spp. infection in laboratory mice

Abnormal synthesis of the main intestinal proteo­glycan mucin-2 is typical of ulcerative colitis and Crohn’s disease in humans. Those morphological changes of the mucus layer affect the diversity of the intestinal microflora. Antibiotics may be ineffective or even dangerous to humans or animals deficient for mucin-2 because of the risk of sepsis and chronic inflammation. In this study, we investigated the potential of antibiotics (clarithromycin, amoxicillin, and metronidazole) in elimination of patho­genic infection from Muc2 knockout mice (Muc2–/–). We assayed the population sizes of pathogens (Heli­co­bacter spp.) and symbiotic (E. coli) bacteria in the intestines of animals as a criterion of antibiotic efficacy. The damaging effect of antibacterial treatment on the host body was estimated from their survival rate. Three antibiotics were ineffective in the elimination of Helicobacter spp. from mucin-2-deficient mice. Moreover, the mortality of Muc2 knockout mice during the antibacterial treatment was 60 %. The survival of wild-type mice (C57BL/6J) during the treatment was 100 %. The weight of wild-type mice showed no decrease during the treatment. The Helico­bacter spp. pathogen was fully eradicated from wild-type mice. Thus, therapy of Helicobacter spp. infection in mucin-2 deficient animals is not only poorly efficient but even deadly. The high susceptibility to antibiotics allows Muc2 knockout mice to be used as a test model to evaluate the pharmacological safety of new antibiotics