


Vol 510, No 1 (2023)
Articles
GENE KNOCKOUT SUPPRESSES EXPRESSION OF DNA BASE EXCISION REPAIR GENES
Abstract
The effect of



INCUBATION OF LYMPHOCYTES WITH IL-2 CAUSES THE APPEARANCE OF ANTITUMOR T CELLS CARRYING FC, CD25 AND LFA-1 ON THE SURFACE
Abstract
To carry out antitumor activity against cells that have lost surface antigens, human lymphocytes must have a certain repertoire of surface proteins capable of contacting a tumor cell and inducing programmed cell death in it. In this work, we showed that activation of healthy donor cells by IL-2 cytokine within 6 days causes the appearance of FasL, CD25 and LFA-1 proteins on CD8+CD25+ T lymphocytes, and also converts the LFA-1 protein into an active form having a high affinity for its target, ICAM-1 integrin. The appearance of these proteins on the surface of this subpopulation of lymphocytes allows them to induce programmed cell death in HLA-negative tumor cells.



BARNASE-BARSTAR SPECIFIC INTERACTION REGULATES CAR-T CELLS CYTOTOXIC ACTIVITY TOWARD MALIGNANCY
Abstract
The development of CAR-T specific therapy made a revolution in modern oncology. Despite the pronounced therapeutic effects, this novel approach displayed several crucial limitations caused by the complications in pharmacokinetics and pharmacodynamics controls. The presence of the several severe medical complications of CAR-T therapy initiated a set of attempts aimed to regulate their activity in vivo. We propose to apply the barnase-barstar system to control the cytotoxic antitumor activity of CAR-T cells. To menage the regulation targeting effect of the system we propose to use barstar-modified CAR -T cells together with barnase-based molecules. Barnase was fused with designed ankyrin repeat proteins (DARPins) specific to tumor antigens HER2 (human epidermal growth factor receptor 2) The application of the system demonstrates the pronounced regulatory effects of CAR-T targeting.



INTERACTOME OF PARAOXONASE PON2 REVEALS NEW PATHWAYS FOR TUMOR GROWTH REGULATION
Abstract
The interactome of paraoxonase-2 encoded by the PON2 gene was investigated. A cDNA library was screened using a yeast two-hybrid system to search for new proteins interacting with human PON2. Analysis of the identified candidates, along with previously published data on interactors obtained by other methods, indicates the presence of a significant number of indirect interactions between PON2 and EGFR and, consequently, possible regulation of tumor growth with mutant EGFR involving PON2.



INFLUENCE OF THE CULTIVATION CONDITIONS OF THE GLIOBLASTOMA NEUROSPHERE ON THE EXPRESSION OF MALAT1 AND LINCROR LONG NON-CODING RNA GENES
Abstract
ABSTRACT Glioblastoma multiforme (GBM) is the most aggressive malignant brain tumor. One of the reasons for the resistance of MGB to treatment is the extreme heterogeneity of the tumor and, in particular, the presence of cancer stem cells (CSCs) in the population of glioblastoma cells. In this work, we investigated the effect of conditions that reduce the proportion of CSCs in the GBM cell population on the levels of long noncoding RNAs (lincROR and MALAT1) involved in the formation of the phenotype of glioblastoma cancer stem cells. We have shown that culturing under conditions that cause a decrease in cell stemness (when fetal calf serum is added to the culture medium) affected the content of these transcripts: in the cells of most of the analyzed lines, a decrease in the level of the positive stemness regulator lincROR and an increase in the content of MALAT1 were noted.



STRUCTURAL MECHANISM OF IONIC CONDUCTIVITY OF THE TRPV1 CHANNEL
Abstract
The so-called “hydrophobic gating” is widely discussed as a putative mechanism to control water and ion conduction via ion channels. This effect can occur in narrow areas of the channels pore lined by non-polar residues. In the closed state of the channel, such regions may spontaneously transit to a dehydrated state to block water and ions transport without full pore occlusion. In the open state, the hydrophobic gate is wide enough to provide sustainable hydration and conduction. Apparently, the transport through the open hydrophobic gate may by facilitated by some polar residues that assist polar/charged substances to overcome the energy barrier created by nonpolar environment. In this work, we investigated the behavior of Na+ ions and their hydration shells in the open pore of the rat TRPV1 ion channel by molecular dynamics simulations. We show that polar protein groups coordinate water molecules in such a way as to restore the hydration shell of ions in the hydrophobic gate that ensures ion transport through the gate in a fully hydrated state.



INFLUENCE OF TYROSYL-DNA PHOSPHODIESTERASE 1 INHIBITOR ON THE PROAPOPTOTIC AND GENOTOXIC EFFECTS OF ANTICANCER AGENT TOPOTECAN
Abstract
To date, various strategies have been proposed to increase the effIciency of cancer therapy. It is known that the action of DNA repair system can determine the resistance of cancer cells to DNA-damaging chemotherapy and radiotherapy, and one of these ways to increase therapeutic efficiency is the search for inhibitors of enzymes of the DNA repair system. Inhibition of the DNA repair enzyme tyrosyl-DNA phosphodiesterase1 (Tdp1) leads to an increase in the effectiveness of the topoisomerase 1 (Top1) inhibitor, the anticancer drug topotecan. Covalent complexes Top1-DNA, which are normally short-lived and are not a threat to the cell, are stabilized under the influence of topotecan and lead to cell death. Tdp1 eliminates such stabilized complexes and thus weaken the effect of topotecan therapy. We have previously shown that the use of the usnic acid hydrazonothiazole derivative



MODULAR NANOTRANSPORTERS CAPABLE OF BINDING WITH SARS-COV-2 VIRUS NUCLEOCAPSID PROTEIN INTO TARGET CELLS
Abstract
Based on the literature data, an antibody-like molecule, a monobody, was selected that is capable of interacting with the nucleocapsid protein (N-protein) of the SARS-CoV-2 virus with high affinity (dissociation constant 6.7 nM). We have previously developed modular nanotransporters (MNTs) to deliver various molecules to a selected compartment of target cells. In this work, a monobody to the N-protein of the SARS-CoV-2 virus was included in the MNT using genetic engineering methods. In this MNT, a site for the cleavage of the monobody from the MNT in endosomes was also introduced. It was shown by thermophoresis that the cleavage of this monobody from MNT by the endosomal protease cathepsin B leads to a 12-fold increase in the affinity of the monobody for the N-protein. Cellular thermal shift assay showed the ability of the obtained MNT to interact with the N-protein in A431 cells transfected with the SARS-CoV-2 N-protein fused to the mRuby3 fluorescent protein.



THE EFFECT OF THE AGONIST CHOLECYSTOKININ-4 D-GB-115 ON THE CHARACTER OF MOTOR ACTIVITY OF
Abstract
The study investigated the effect of GABA in various concentrations and D-GB-115 at a concentration of 10–10 mol/ml on the behavior of



SIMULATED MICROGRAVITY AND COCULTURING WITH HEMATOPOIETIIC CELLS OPPOSITELY MODULATE WNT SIGNALING IN MESENCHYMAL STROMAL CELLS
Abstract
The osteogenic potential of mesenchymal stromal cells (MSCs) can determine the bone homeostasis and the physical characteristics of bones. Microgravity reduces the ability of these cells to differentiate in osteogenic direction. It has been shown that the addition of hematopoietic stem and progenitor cells (HSPCs) to MSC culture in vitro can have the opposite effect. The aim of this study was to identify transcriptional changes in 84 genes associated with Wnt signaling in MSCs during microgravity simulation and interaction with HSPCs. The results indicate an increase in the non-canonical Wnt signaling activity during MSCs and HSPCs cocultivation, while simulated microgravity enhances the canonical component of this signaling pathway. These changes may underlie the modulation of osteogenic potential of MSCs in hematopoietic niche under microgravity.



WATERFOWL WINTERING IN CITIES OF TEMPERATE CLIMATE ZONE AND FACTORS THAT DETERMINE THEM
Abstract
For the first time, the regularities of the number and species diversity dynamics of wintering waterfowl in 30 cities of Russia over eight years have been analyzed. The total number increased by 35%. The species diversity in total reaches 32 species. Mallards (



SEASONAL VARIABILITY OF IMMUNOHEMATOLOGICAL PARAMETERS OF PERPHERAL BLOOD OF THE BAT (BOIE, 1825) LIVING IN THE URALS
Abstract
A comparative analysis of the immunohematological parameters of bats from fauna of the Urals



THE LIFETIME OF COLOUR MORPHS IN THE POLYMORPHIC POPULATIONS OF THE MOLE VOLE AND THE HYPOTHESIS OF ADAPTIVE POLYMORPHISM
Abstract
For the first time, different lifetime was established in representatives of three colour morphs (brown, bicolor, black) in 10 populations of the Mole Vole of the Volga region, the Urals and the Trans-Urals. With the longest life span of the species – 5 years, numerically dominant morphs in the population are able to live 1–4 years longer than the accompanying ones. Spearman’s correlation coefficient between the longest life span of morphs and their proportion in the population was



THE FIRST DATA ON THE NUTRITION OF THE URAL CAVE BEAR (MAMMALIA, CARNIVORA, URSIDAE, () KANIVETZ VERESTCHAGIN, 1973) BASED ON THE RESULTS OF THE ANALYSIS OF ISOTOPES C and N
Abstract
The first data on the content of isotopes 13C and 15N in the collagen of 16 bones of the Ural cave bear (



CAN SHREWS AVOID COMPETITION WHEN VIOLATING THE HUTCHINSON’S ECOLOGICAL RULE?
Abstract
It is established that the rule of G. Hutchinson’s idea of the ratio of body weight and size and foraging organs of similar species is not fully respected when comparing the species of shrews of the genus



NON-SELECTIVE EXPRESSION OF SHORT-WAVELENGTH CONE OPSIN IMPROVES LEARNING IN MICE WITH RETINAL DEGENERATION IN A VISUALLY GUIDED TASK
Abstract
Here, we explore the potential of an animal opsin non-selectively expressed in various neuronal elements of the degenerative retina to restore impaired visual function. In this study, a knockout murine model of inherited retinal distrophy was used. Animals were injected intravitreally with either a virus carrying gene of the short-wavelength cone opsin associated with a reporter fluorescent protein, or a control virus carrying the sequence of a modified fluorescent protein that had an enhanced membrane tropism. The viral transduction induced pronounced opsin expression in ganglion, bipolar, and horizontal retinal neurons. Behavioral testing of the treated mice in the visually guided task in the trapezoid Morris water maze showed a partial recovery of learning ability in animals whose retinas had been transduced with the cone opsin.



ALLELOTOXICITY OF GREENHOUSE SUBSTRATES AFTER VEGETABLE CULTIVATION
Abstract
It is known that stresses during the cultivation of agricultural plants reduce yields, and the occurrence of stressful effects leads to the release of allelotoxins by plants into the soil. It has been suggested that this factor can have a noticeable effect on the vegetation of vegetables in greenhouses, and a decrease in the concentration of allelotoxins in greenhouse substrates can improve the vegetation of plants. To verify these assumptions, the allelotoxicity of greenhouse substrates and the content of microorganisms in them under well and poorly vegetating plants of cucumbers, tomatoes and peppers were determined. It was found that there are significantly more allelotoxins and fewer prokaryotes in the substrates under poorly vegetating plants, which confirmed the assumption about the significance of the allelotoxins influence on the cultivation of vegetables in greenhouses. The introduction of humate solutions with a high sorption capacity in relation to allelotoxins into the root zone of plants makes it possible to significantly improve the vegetation of cucumbers and may be a promising direction for increasing vegetable yields in greenhouses.



SUBSP. NOV. (VESPERTILIONIDAE, CHIROPTERA) FROM THE LOWER PLEISTOCENE OF THE TAURIDA CAVE IN CRIMEA
Abstract
A new northern serotine bat



IDENTIFICATION OF SIGNIFICANT RNA-BINDING PROTEINS IN THE PROCESS OF CD44 SPLICING USING THE BOOSTED BETA REGRESSION ALGORITHM
Abstract
The expression of RNA-binding proteins and their interaction with the spliced pre-mRNA are the key factors in determining the final isoform profile. Transmembrane protein CD44 is involved in differentiation, invasion, motility, growth and survival of tumor cells, and is also a commonly accepted marker of cancer stem cells and epithelial-mesenchymal transition. However, the functions of the isoforms of this protein differ significantly. In this paper, we developed a method based on the boosted beta regression algorithm for identification of the significant RNA-binding proteins in the splicing process by modeling the isoform ratio. The application of this method to the analysis of CD44 splicing in colorectal cancer cells revealed 20 significant RNA-binding proteins. Many of them were previously shown as EMT regulators, but for the first time presented as potential CD44 splicing factors.



184–188 NUCLEOTIDES DELETION OF HUMAN TELOMERASE RNA DOES NOT AFFECT ON THE TELOMERASE FUNCTIONING
Abstract
Telomerase is a ribonucleoprotein complex, the main components of which are telomerase RNA and reverse transcriptase. Previously, it was shown in our laboratory that human telomerase RNA contains an open reading frame, starting at adenine in position 176. The open reading frame encodes the hTERP protein, and the deletion of nucleotides 184–188 of human telomerase RNA disrupts the open reading frame and leads to the absence of hTERP. Human telomerase RNA has a conserved structure, changes in which affect telomerase activity. In this work, we have shown that the deletion of nucleotides 184–188 of telomerase RNA does not affect the functioning of telomerase.


