Vol 10, No 5 (2016)

During prolonged cultivation, cell lines may lose a number of innate characteristics or acquire new ones. In this work, we compared growth and phenotypic characteristics of human glioblastoma А172 and Т98G cell lines received from the cell culture collection of the Research Institute of Influenza (St. Petersburg, Russia). The activity of genes encoding intracellular proteins that define belonging of these cell lines to mesenchymal type, as well as activity of several growth factor genes and extracellular matrix genes was evaluated. Cell lines A172 and T98G varied in morphology and surface markers expression. High level of mesenchymal markers CD90 and CD105, fibroblast activation protein, and tenascin C was detected for A172 cell line. Both cell lines expressed high level of α2 smooth muscle actin gene. Data demonstrating high activity of genes encoding major angiogenesis inductors (VEGF, FGF2(b), TGFβ1) and thrombospondin-1 in cell lines under study are in agreement with published data. Reduction of fetal serum content in culture medium from 10 to 5% increased the number of cells with CD73 and CD105 surface antigens in both cell lines. A172 and T98G cell lines maintain the main features of glioblastomas and therefore can be used as research objects in investigation of this type of neoplasms.

Human adipose-derived mesenchymal stem cells (MSCs) can be stimulated to differentiate into hepatic cells. MSC differentiation was induced by fibroblast growth factor-4, hepatocyte growth factor, oncostatin M, and dexamethasone. The influence of quercetin on MSC hepatic differentiation in culture was assayed, and 1 or 10 μmole/L quercetin added into the induction medium enhanced the manifestation of MSC hepatic differentiation. Urea secretion, cytokeratin 19 expression, and α-fetoprotein synthesis were increased. Quercetin modulated CYP1A–cytochrome P450 activity in the differentiated cells. MSCs differentiated in the presence of quercetin exhibited higher viability and resistance to oxidative stress.

The formation and functional plasticity of the blood–brain barrier are inextricably linked to the molecular events occurring in cerebral neurovascular unit during the embryonic and early postnatal development of the organism. To study the features of the barrier genesis under physiological conditions, as well as after perinatal hypoxia and stress in early life, tight junction proteins of cerebral endothelial cells (the number of JAM-, ZO1-, and CLDN5-positive cells) in rats at the age of 7 (P₇), 28 (P₂₈), and 70 (P₇₀) days were investigated. It was found that, under physiological conditions, the number of cells expressing JAM, ZO1, and CLDN5 slightly increase in the period from P₇ to P₇₀ in the cortex, hippocampus, and amygdala of the brain. After perinatal hypoxia, the number of cells expressing the proteins of tight junctions (JAM, CLDN5) is significantly increased to the age of P₂₈–P₇₀, while the number of ZO1⁺ cells in the same period of time is reduced. Early life stress causes an imbalance between the expression of ZO1 and other proteins of tight junctions, but these changes are opposite in direction.

Vascular endothelial growth factor (VEGF) in adults is synthesized in small amounts by thymic epithelial cells and is important for the maintenance of vascular homeostasis. However, its role dramatically increases during the process of thymic reconstitution after damage caused by radiation, chemo-, or hormonotherapy. The aim of the study was to evaluate the influence of different factors on VEGF production by mouse thymic epithelial cells in vitro. As a model, two cell lines were used: cortical cTEC1-2 and medullar mTEC3-10 cells. These cells were characterized by their ability to synthesize VEGF mRNA and VEGF protein, as well as by the presence of VEGF receptors. No VEGFR1 or VEGFR2 mRNA expression was observed in these cells, while NRP-1 mRNA was expressed at a low level. An ELISA test showed that cTEC1-2 cells produced VEGF about 30 times more than mTEC3-10 cells. These cell lines, when exposed to cytokines, hormonal factors, or thymocytes, responded differently. Keratinocyte growth factor (KGF) enhanced VEGF mRNA expression, as well as VEGF protein production, in medullar cells, but down-regulated VEGF mRNA synthesis in cortical cells. Dexamethasone suppressed the levels of VEGF mRNA expression and its protein production in cortical cells, while in medullar cells only VEGF production was reduced. Introduction of IL-7, IL-1β, or murine thymocytes increased, while administration of semaphorin-3A, SDF-1α, or ACTH decreased, VEGF production by cortical epithelial cells with no influence on medullar cells. We suggest that our data, obtained in vitro, can serve for further development of special strategies directed for regulation of VEGF synthesis in the thymic epithelial cells in vivo.

Using fluorescent microscopy, we found decreased expression of the β1 subunit of Na⁺/K⁺-ATPase and subunits of Ca²⁺-ATPase, increased expression of the α1S subunit of the L-type Ca²⁺-channel, and no changes in the expression of the α2 subunit of Na⁺/K⁺-ATPase in rat postural muscle under the conditions of modeled hypogravity. In the phasic muscle, we observed decreased expression of the β1 subunit, which was similar to that found in the postural muscle, whereas the other studied parameters remained without alterations. However, a decrease in the fluorescence intensity of the β1 subunit was insignificant due to a high variability of data. Thus, hypogravity negatively influenced primarily those skeletal muscles that are responsible for static load.

The possibility of using bone marrow stem cells for treatment of Duchenne muscular dystrophy is intensely studied. Mdx mice are the most widely used laboratory model of Duchenne muscular dystrophy. One approach of cell therapy of muscular dystrophy is substitution of bone marrow in mdx mice after their X-ray irradiation. However, this method does not allow one to increase significantly dystrophin synthesis in muscular fibers of mdx mice. To improve the effect of transplanted cells on muscle regeneration, we additionally treated mdx mice subjected to transplantation of bone marrow cells with a weak combined magnetic field tuned to ion parametric resonance for Ca²⁺ (Ca²⁺-CMF). We found that, in irradiated chimeric 3 and 5 Gy mdx mice, additional treatment with Ca²⁺-CMF for 1 month resulted in significant increases in the portions of dystrophin-positive muscle fibers, by 15.8 and 18.3%, respectively, as compared to the control groups. Furthermore, the share of muscle fibers without centrally located nuclei also increased. We suggest that the magnetic field with these parameters may stimulate functioning of nuclei of donor cells, which were incorporated into muscle fibers.

The dynamics of changes in the stress protein content in the gill epithelium cells of the bivalve Mytilus edulis in the course of phenotypic adaptation to changes in environmental salinity was studied. It was demonstrated that, at low seawater salinity (10‰), which provokes the isolation reflex, induction of the Hsp70 family stress protein expression is achieved on the fifth day. The results of parallel measurements of the mussel extravisceral liquid osmolarity showed that the factor triggering stress proteins expression in the mollusks under study is not the seawater salinity, but rather osmolarity of their internal environment.