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Proteomics of the effect of compensated and static magnetic fields on cell proliferation in vitro

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Author(s):
David Lucas Desiderio
Total Authors: 1
Document type: Doctoral Thesis
Press: Bauru.
Institution: Universidade de São Paulo (USP). Faculdade de Odontologia de Bauru (FOB/SDB)
Defense date:
Examining board members:
Marilia Afonso Rabelo Buzalaf; Flavio Augusto Cardoso de Faria; Ivan Amaral Guerrini; Vanessa Soares Lara; Heloisa Aparecida Barbosa da Silva Pereira
Advisor: Marilia Afonso Rabelo Buzalaf; Andre Luiz Malvezzi
Abstract

Inserted in the transdisciplinarity paradigm, the present work was developed by steps with the following aims: a) To build a device of non-magnetic metal to hold permanent magnets for the generation of a Static Magnetic Field (SMF) or a Compensated Magnetic Field (CMF); b) To expose mesenchimal cells to the SMF and to CMF or to none of the fields (control); c) To analyze the influence of these fields on cell viability and cell proliferation and in the case where it occurred alteration in at least one of these parameters, to use proteomics as a tool for the comprehension of the involved mechanisms. The device was built in stainless steel, able to generate two kinds of Magnetic Fields: Compesated (CMF) with an intensity of nearly zero mT and Static (SMF) with a mean intensity of 165 mT. These fields were applied to bone marrow mesenchimal cell cultures from AJ mice (MSC/AJ), for 0, 24, 48, 72 and 96 h (CMF) and 24 h (SMF) periods. The effects on the proliferation and viability were assessed by tripan blue dying and manual counting of the cells. Proteomics was done for the experiments with CMF, aiming to describe the involved proteins on found alterations. The exposition to CMF tends to reduce the bone marrow cell proliferation of MSC/AJ in relation to control in 96 h, but with no significant difference, which may be related to proteins that inhibit the transcription, like Forkhead box protein P2 Foxp2. This very field raised the cell viability in relation to the baseline for all the experimental times that could be related to proteins connected to Ca2+ binding. However, these mechanisms need more experiments, so they can be confirmed or not. The exposition to the SMF tends to decrease both cell proliferation and viability in relation to the control group, although with no significant difference, probably because of the sample number and the exposition time (24h). (AU)

FAPESP's process: 13/24038-7 - Proteomics of the Effect of Static and Compensated Magnetic Fields in Cell Proliferation in vitro
Grantee:David Lucas Desidério
Support Opportunities: Scholarships in Brazil - Doctorate