RESUMO
Immune aggression to transplanted allogeneic bone marrow, i.e. the graft-versus-host disease (GVHD), could be decreased by the suppression of effector and/or activation of T- regulatory cells (Treg). This task could be solved by co-transplantaiton of allogeneic bone marrow and mesenchymal stromal cells (MSCs). This study demonstrated the elevated immune modulating activity of MSCs by their culturing in vitro on Al203 oxide nanocoatings. Introduction of the cells to the animals with GVHD resulted in an increased content of Treg in the spleen of bone marrow recipients, reduced severity of the pathology, and higher survival of animals. Thefindings could be the basis for developing the new approaches to optimize the GVHD treatment methods involving the oxide nanocoating cultured MSCs.
Assuntos
Óxido de Alumínio/química , Técnicas de Cultura de Células/métodos , Doença Enxerto-Hospedeiro/terapia , Transplante de Células-Tronco Mesenquimais/métodos , Células-Tronco Mesenquimais/citologia , Nanoestruturas/química , Animais , Modelos Animais de Doenças , Doença Enxerto-Hospedeiro/imunologia , Camundongos Endogâmicos C57BL , Camundongos Endogâmicos CBA , Linfócitos T Reguladores/imunologia , Transplante HomólogoRESUMO
BACKGROUND: Fetoplacental tissues including the early chorion contain stem cells with various morphological and functional characteristics. Cultured chorionic cells may be used in perspective therapies of different pathologies. OBJECTIVE: To investigate the effect of cryopreservation on proliferation and differentiation potential of chorion cell culture (ChCC). MATERIALS AND METHODS: Five freezing programs for ChCC were compared: Program 1, cooling from 25 degrees C down to -30 degrees C at 0.5 degrees C/min; Program 2, cooling from 25 degrees C down to -30 degrees C at 1 degrees C/min; Program 3, cooling from 25 degrees C down to -10 degrees C at 1 degrees C/min with further cooling down to - 80 degrees C at 10 degrees C/min; Program 4, cooling from 25 degrees C down to -5 degrees C at 1 degrees C/min with further cooling down to -80 degrees C at 10 degrees C/min; Program 5, cooling from 25 degrees C down to -6 degrees C at 1 degrees C/min with further crystal seeding by adding the surplus nitrogen into the chamber, and cooling down to -80 degrees C at 10 degrees C/min. Viability, adhesion, proliferation and directed differentiation were examined. RESULTS: Freezing program 5 achieved the best result, with the highest viability, adhesion, proliferation and directed differentiation. CONCLUSION: The data may help establishing better cryopreservation protocols for perspective chorionic cell lines and their further application in biotechnology.
Assuntos
Córion/citologia , Criopreservação/métodos , Adesão Celular , Técnicas de Cultura de Células , Diferenciação Celular , Proliferação de Células , Sobrevivência Celular , Células Cultivadas , Congelamento , HumanosRESUMO
Tumor development is the consequence of expanding the population of low differentiated cells with unlimited self-maintenance potential, i.e. cancer stem cells (CSCs). Application of new forms of nanocomposites capable of binding to CSCs and inducing the tumor destruction is perspective direction for treating this pathology. There have been developed the methods of obtaining hybrid nanocomplexes containing rare-earth orthovanadates GdYVO4:Eu³âº, cholesterol and luminescent dye Dil. By immune fluorescence method using monoclonal antibodies to CD44, CD24, CD117 and Sca-1 markers there has been established the change in the ratio of tumor progenitors of various differentiation levels in a general pool of Ehrlich carcinoma (EC) after treatment with hybrid nanocomplexes. Essential reduction in the concentration of the most tumorogenic CD44high cells with simultaneous rise in the number of CD117âº-cells resulted in an increased index of CD44high/CD117⺠ratio. It has been demonstrated that application of hybrid nanocomplexes suppressed the tumor growth almost by 80%. The value of cooperative interactions of the cells with different phenotype signs in tumor sites has been proved. The index of CD44high/CD117⺠ratio can be used as one of diagnostic and prognostic parameters of development and inactivation rate of tumor process when using different types of anti-tumor therapy.