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Biomedical subjects

R V Deev

Publications and source records attributed to R V Deev.

5 recordsLinked to original sources
PubMed2005

[Participation of transfused bone marrow cells in reparative osteohistogenesis].

The participation of skeletal tissue cell precursors in the repairing regeneration of bone tissue was studied. Bone marrow was taken from donor animals--mice of C57Bl/6-TgN(ACTbGFP) 1 Osb line (The Jackson Laboratory Bar Harbor ME USA line). Nucleated cell fraction was isolated by centrifugation on a density percoll gradient. Recipient mice C57Bl/6 line were irradiated by 7.0-7.5 Gr dose. Intravenous infusion of donor cells and osteoclasts of tibia was done after irradiation of recipient mice. Histological preparations of bone regenerate tissues were studied on 15, 30, and 60 days by confocal microscopy. Donor cells were found as skeletal tissue precursors into periost, endost, bone marrow, and as differentiated cells of newborn tissue of regenerate--osteoblasts, osteocytes, chondrocytes. The data obtained indicate that part of donor bone marrow cells are able to progressive differentiation under recipient bone fractures.

Animals↗
PubMed2004

[Development and morphofunctional characterization of the osteoblastic phenotype in cell culture in vitro].

The objective of this research was to study osteogenic properties of cultured rabbit bone marrow stromal cells, newborn rat cranium bone cells and rat osteocarcoma ROS 17-2/8 cells. For this purpose cytochemical reaction for alkaline phosphatase was performed by the Lowry method, mineral deposition was assessed by staining of the cultures after von Kossa. Cranium bone cells were shown to synthesize alkaline phosphatase (34 +/- 7 nmol/min/10(6) cells), the matrix mineralization being found. Bone marrow stromal cells displayed a lower activity alkaline phosphatase level than did cranium bone cells (4 +/- 0.6 nmol/min/10(6) cells). However, cell cultivation in the presence of dexamethasone in the medium (10(-8) M) induced a higher activity of alkaline phosphatase (9 +/- 1 nmol/min/10(6) cells), mineralization of the extracellular matrix being the case. The highest level of alkaline phosphatase activity was found for ROS 17-2/8 cells (60 +/- 12 nmol/min/10(6) cells) but no matrix mineralization was determined. According to these data, matrix calcification and formation of bone-like nodules are the most important properties of osteoblastic differentiation in vitro.

Alkaline Phosphatase↗
PubMed2004

[Lamellar bone culture in vitro].

The objective of this study was to analyze morpho-functional characteristics of the cells in definitive osseous tissue cultured in vitro. Cortical plates, isolated from the fragments of iliac bones of adult rabbits, were cultured in vitro in a nutrient medium. The culture obtained was fixed after 3, 10 and 20 days and processed for scanning electron microscopy. To identify the osteogenic cells, alkaline phosphatase activity was demonstrated. It was established that the processes of cell proliferation and migration from the cultured bone pieces were most active at 10 days after the explanation. The growing cells formed a growth zone around the bone fragment that consisted of three layers, differing in the degree of cellular proliferation and differentiation. After 20 days in culture the cells expressing alkaline phosphatase were shown to form groups. The cells of osteon canals in culture were found to possess potential for proliferation and osteogenic differentiation.

Alkaline Phosphatase↗
PubMed2003

[Stromal stem cells and osteoblastic cellular differon].

The article presents an analysis of the data on the origin, differentiation, morpho-functional characteristics and reactivity of the bone cells taking into account theoretical concepts of histogenetic series and cell differons. The information on the sources and proliferation of cells of the osteogenic line was used as the basis for development of a variant of a scheme describing the differentiation of these cells from a stromal stem cell (SSC) to a bone-lining cell and osteocyte. Considering possible differentiation of SSC into the cells of fibroblastic, chondroblastic, adipocytic and leiomyocytic cell lines, the unified model of mechonocytogenesis is proposed.

Cell Differentiation↗