[Effect of human brain extracts on cultured neuroblastoma cells]. / Vliianie ékstraktov golovnogo mozga cheloveka na kletki kul'tury neiroblastomy.

OBJECTIVE: To identify the effect of brain extracts from people of different age groups on possible changes in cell physiology and behavior in vitro. MATERIAL AND METHODS: Human frontal cortical segments were obtained 12-24 hours after autopsy. Brain tissue extract was taken from young people who died at age of 22.5±2.7 years and old people at 80.9±3.0 years. SK-N-MC human neuroblastoma cells were cultured in a medium containing 50 mg/ml of brain tissue extracts; blood serum (50 mg/ml) from healthy people was used as a control. Procedures for cytophotometry of DNA and acidic proteins and polarized light microscopy were used. RESULTS: A short-term decrease in acidic protein levels in the nucleus and nucleolus was found to be affected by brain extracts from old people. There were higher cytoplasmic acidic protein levels. At the same time, the same indicators generally remained noticeably unchanged under the influence of brain extracts from young people. There were also simultaneous pronounced changes in cell morphology and behavior in vitro; namely, neuronal cell processes became shorter and their proliferative activity increased, which was not least a result of the unblocking of cells in the G2 phase under the influence of brain extracts from old people. CONCLUSION: The factors that accelerate cell proliferation in vitro accumulate in the human brain with age. Simultaneously with the acceleration of cell proliferation, there are changes in cell metabolic activity and morphology.

Hemophagocytic lymphohistiocytosis in acute African swine fever clinic.

INTRODUCTION: Hemophagocytic lymphohistiocytosis (HLH) usually has been defined as the combination of a proliferation of cytologically benign, actively phagocytic macrophages in bone marrow, spleen, lymph nodes, etc. in association with fever, cytopenia, splenomegaly, and hypertriglyceridemia. HLH is often triggered by viral infection. The aim of this study was to ascertain the features of HLH involvement in African swine fever virus (ASFV) (genotype II) pathogenesis. METHODS: The serum levels of macrophage colony-stimulating factor (MCSF) and granulocyte-macrophage colony-stimulating factor (GMCSF), as well as the histological constitution (for hemophagocytic macrophages detection) of various organs of pigs infected with ASFV genotype II were investigated. The diagnosis of HLH was made according to universally accepted human criteria. RESULTS: The association of fever, cytopenias, splenomegaly, and hemophagocytosis was present in 87.5% of the infected pigs (absence of hyperthermia in one of eight pigs). Marked hypertriglyceridemia was observed at 3-4days post infection. Previously it was shown that ASFV induced a significant decrease in the level of fibrinogen from day 5 till the end of experiment. Progression of the HLH coincided with a temporary increase in the serum levels of MCSF levels (early stage of disease) and GMCSF levels (2-3 pays post infection). CONCLUSIONS: Hemophagocytic syndrome should be suspected in ASFV (genotypeII) infected pigs.

Comparative multiparametric analysis of HeLa and RD cell culture reactions to solcoseryl.

Reactions of continuous HeLa and RD cell cultures and their nuclear and nucleolar apparatus to addition of solcoseryl into the medium were studied. The monolayer density, proliferation activity, percentage of dead cells, RNA and DNA content in the nuclei and nucleoli, number of nucleoli in the nuclei, cell distribution in the population by the number of nucleoli in the nuclei, volume and complete surface area of the nuclei and nucleoli, and the nucleolar/nuclear ratio were evaluated. The cultures differently reacted to solcoseryl in the medium at the population and cellular levels of their organization. By the results of multiparametric analysis of the reactions of cells and their nuclear and nucleolar apparatus, solcoseryl can be referred to bioactive substances with characteristics of a factor regulating cell population growth.