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The human immunodeficiency virus (HIV) epidemic is a global issue. The estimated number of people with HIV is 39,000,000 to date. Antiviral therapy is the primary approach to treat the infection. However, it does not allow for a complete elimination of the pathogen. The advances in modern gene therapy methods open up new possibilities of effective therapy. One of these areas of possibility is the development of technologies to prevent virus penetration into the cell. Currently, a number of technologies aimed at either the prevention of virus binding to the CCR5 coreceptor or its knockout are undergoing various stages of clinical trials. Since HIV can also utilize the CXCR4 coreceptor, technologies to modify this receptor are also required. Standard knockout of CXCR4 is impossible due to its physiological significance. This review presents an analysis of interactions between individual amino acids in CXCR4 and physiological ligands and HIV gp120. It also discusses potential targets for gene therapy approaches aimed at modifying the coreceptor.

Helicobacter pylori is a microaerophilic, spiral-shaped and gram-negative microorganism that produces various virulence factors such as CagA, VacA, urease, and host cells adhesins, which in a synchronous concert, allow H. pylori to colonize and infect the host gastric epithelium. H. pylori infection is associated with some severe side effects in human, such as gastritis, peptic ulcer, non-Hodgkin's lymphoma and adenocarcinoma. CagA is the most notorious virulence factor of H. pylori. It is known as the first bacterial oncoprotein. The gene encoding CagA is localized on the cag pathogenicity island (cagPAI), a 40kbp DNA segment which also carries genes for the type four secretion system (T4SS) of H. pylori. The interaction of CagA with intracellular partner proteins leads to some irreversible alteration of host cells by increasing cell size, elevating motility, phenomena known as the \"hummingbird phenotype\". CagA also disrupts the epithelium apical junctions and thereby destroys the normal epithelial architecture. A tyrosine phosphorylation site, named EPIYA motif, helps CagA to bind to cytosolic proteins in a phosphorylation-dependent manner. CagA is also interacts with host proteins in a phosphorylation-independent fashion, which altogether will assist to develop adenocarcinoma in infected cells. This review summarizes the core data on the structure and function of CagA and its role in conferring the main pathophysiologic effects of H. pylori infection as well as suggesting a therapeutic option for treatment of H. pylori infection based on CagA virulence.

Helicobacter pylori is a microaerophilic, spiral-shaped and gram-negative microorganism that produces various virulence factors such as CagA, VacA, urease, and host cells adhesins, which in a synchronous concert, allow H. pylori to colonize and infect the host gastric epithelium. H. pylori infection is associated with some severe side effects in human, such as gastritis, peptic ulcer, non-Hodgkin’s lymphoma and adenocarcinoma. CagA is the most notorious virulence factor of H. pylori. It is known as the first bacterial oncoprotein. The gene encoding CagA is localized on the cag pathogenicity island (cagPAI), a 40kbp DNA segment which also carries genes for the type four secretion system (T4SS) of H. pylori. The interaction of CagA with intracellular partner proteins leads to some irreversible alteration of host cells by increasing cell size, elevating motility, phenomena known as the “hummingbird phenotype”. CagA also disrupts the epithelium apical junctions and thereby destroys the normal epithelial architecture. A tyrosine phosphorylation site, named EPIYA motif, helps CagA to bind to cytosolic proteins in a phosphorylation-dependent manner. CagA is also interacts with host proteins in a phosphorylation-independent fashion, which altogether will assist to develop adenocarcinoma in infected cells. This review summarizes the core data on the structure and function of CagA and its role in conferring the main pathophysiologic effects of H. pylori infection as well as suggesting a therapeutic option for treatment of H. pylori infection based on CagA virulence

Present day biomedical applications, including magnetic biosensing, demand better understanding of the interactions between living systems and magnetic nanoparticles (MNPs). In this work spherical MNPs of maghemite were obtained by a highly productive laser target evaporation technique. XRD analysis confirmed the inverse spinel structure of the MNPs (space group Fd-3m). The ensemble obeyed a lognormal size distribution with the median value 26.8 nm and dispersion 0.362. Stabilized water-based suspensions were fabricated using electrostatic or steric stabilization by the natural polymer chitosan. The encapsulation of the MNPs by chitosan makes them resistant to the unfavorable factors for colloidal stability typically present in physiological conditions such as pH and high ionic force. Controlled amounts of suspensions were used for in vitro experiments with human blood mononuclear leukocytes (HBMLs) in order to study their morphofunctional response. For sake of comparison the results obtained in the present study were analyzed together with our previous results of the study of similar suspensions with human mesenchymal stem cells. Suspensions with and without chitosan enhanced the secretion of cytokines by a 24-h culture of HBMLs compared to a control without MNPs. At a dose of 2.3, the MTD of chitosan promotes the stimulating effect of MNPs on cells. In the dose range of MNPs 10–1000 MTD, chitosan “inhibits” cellular secretory activity compared to MNPs without chitosan. Both suspensions did not caused cell death by necrosis, hence, the secretion of cytokines is due to the enhancement of the functional activity of HBMLs. Increased accumulation of MNP with chitosan in the cell fraction at 100 MTD for 24 h exposure, may be due to fixation of chitosan on the outer membrane of HBMLs. The discussed results can be used for an addressed design of cell delivery/removal incorporating multiple activities because of cell capability to avoid phagocytosis by immune cells. They are also promising for the field of biosensor development for the detection of magnetic labels.

Development of the modern global entrepreneurship is one of the most perspective and promising means of overcoming the consequences of the global economic crisis, as well as prevention of future crises of economic systems, as it ensures full level of optimization of production and distribution processes. The purpose of the article is to determine perspectives of sustainable development of the global entrepreneurship. For determining the level of sustainability of development of the modern global entrepreneurship, the authors use the methods of statistical analysis of time rows (method of horizontal and trend analysis). The authors perform a complex analysis of dynamics of development of global companies and performed evaluation of their sustainability. Also, the necessity for changing the model of managing the development of modern global entrepreneurship for increasing its sustainability is substantiated. As a result, it is concluded that modern global entrepreneurship is developing in the unstable way, and practical recommendations are offered for solving this problem. A perspective model of sustainable development of the modern global entrepreneurship is developed and presented. A certain limitation of the results of the performed research is the framework character of the offered recommendations.

Audiogenic epilepsy (AE), inherent to several rodent strains is widely studied as a model of generalized convulsive epilepsy. The molecular mechanisms that determine the manifestation of AE are not well understood. In the present work, we compared transcriptomes from the corpora quadrigemina in the midbrain zone, which are crucial for AE development, to identify genes associated with the AE phenotype. Three rat strains without sound exposure were compared: Krushinsky-Molodkina (KM) strain (100% AE-prone); Wistar outbred rat strain (non-AE prone) and “0” strain (partially AE-prone), selected from F2 KM × Wistar hybrids for their lack of AE. The findings showed that the KM strain gene expression profile exhibited a number of characteristics that differed from those of the Wistar and “0” strain profiles. In particular, the KM rats showed increased expression of a number of genes involved in the positive regulation of the MAPK signaling cascade and genes involved in the positive regulation of apoptotic processes. Another characteristic of the KM strain which differed from that of the Wistar and “0” rats was a multi-fold increase in the expression level of the Ttr gene and a significant decrease in the expression of the Msh3 gene. Decreased expression of a number of oxidative phosphorylation-related genes and a few other genes was also identified in the KM strain. Our data confirm the complex multigenic nature of AE inheritance in rodents. A comparison with data obtained from other independently selected AE-prone rodent strains suggests some common causes for the formation of the audiogenic phenotype.

The osteogenic, cytotoxic, and antibacterial activities of polysaccharide (PS-SC) and flavonoid (F-SC) fractions isolated from the leaves extract of Saussurea controversa were studied in vitro. F-SC consists of the five quercetin glycosides in the ratio 2:8:10:1:4, which were isolated from the leaves extract of S. controversa and have been characterized previously. PS-SC was first isolated from the leaves extract of S. controversa and has been described. PS-SC consists in 30 compounds is characterized by a high degree of heterogeneity with a heterogeneity index of 19.74. The Mw and Mn of PS-SC were 108.6 and 5.5 kDa, respectively. Structural fragments are represented by galactose, arabinose, xylose, glucose, uronic acids, mannose, and rhamnose in a 10.1:3.3:2.2:2.1:1.7:0.9:0.5 molar ratio. F-SC as compared with PS-SC showed in vitro microbicidal (50 g/L) and better bacteriostatic (6.25 g/L versus 25 g/L of PS-SC) effects against the 24-h growth of Staphylococcus aureus strain 209 P and a 21-day absence of cytotoxicity on human adipose-derived multipotent mesenchymal stromal cells (hAMMSCs). Both fractions (PS-SC > F-SC) at doses of 10–50 mg/L stimulated differentiation of hAMMSCs into secreting osteoblasts accompanied by local mineralization of extracellular matrix. These fractions of S. controversa and especially F-SC, might be promising peroral drugs in the complex treatment of bone fractures and for prophylaxis of their infectious complications.

Animal models of epilepsy are of great importance in epileptology. They are used to study the mechanisms of epileptogenesis, and search for new genes and regulatory pathways involved in the development of epilepsy as well as screening new antiepileptic drugs. Today, many methods of modeling epilepsy in animals are used, including electroconvulsive, pharmacological in intact animals, and genetic, with the predisposition for spontaneous or refractory epileptic seizures. Due to the simplicity of manipulation and universality, genetic models of audiogenic epilepsy in rodents stand out among this diversity. We tried to combine data on the genetics of audiogenic epilepsy in rodents, the relevance of various models of audiogenic epilepsy to certain epileptic syndromes in humans, and the advantages of using of rodent strains predisposed to audiogenic epilepsy in current epileptology.

Phytaspases, plant cell death-promoting and proprotein-processing proteolytic enzymes of the plant subtilase family, display aspartate (caspase-like) cleavage specificity and a very unusual retrograde trafficking from the apoplast to the cell interior upon induction of death-inducing stresses. To determine the underlying molecular mechanisms, we performed a search for tobacco phytaspase (NtPhyt) interactors using an in vivo cross-linking approach in Nicotiana tabacum plants. Tobacco Tubby-like F-box protein 8 (named Tubic hereafter) was identified as an NtPhyt interactor, with formation of the cross-linked complex being only efficient under the oxidative stress conditions. Direct interaction of the two proteins was further corroborated in the in vitro experiments. Analysis of Tubic-EGFP behavior in plant cells revealed that Tubic is a membrane-associated and fairly unstable protein. Furthermore, we showed that NtPhyt and Tubic are capable of negatively affecting one another in plant cells. On the other hand, down-regulation of Tubic in Tubic-silenced plants impaired specifically the retrograde transport of NtPhyt upon the induction of oxidative stress, testifying to a critical role of Tubic in this process. Our study, thus, contributes to understanding of the mechanisms of NtPhyt retrograde trafficking in plant cells subjected to stress.