TY - JOUR
T1 - Effects of static magnetic fields on natural or magnetized mesenchymal stromal cells
T2 - Repercussions for magnetic targeting
AU - Silva, Luisa H.A.
AU - Silva, Sueli M.
AU - Lima, Emilia C.D.
AU - Silva, Renata C.
AU - Weiss, Daniel J.
AU - Morales, Marcelo M.
AU - Cruz, Fernanda F.
AU - Rocco, Patricia R.M.
N1 - Publisher Copyright:
© 2018
PY - 2018/10
Y1 - 2018/10
N2 - The magnetic targeting (MT) technique improves delivery of mesenchymal stromal cells (MSCs) to target sites. However, the moderate-intensity static magnetic fields (SMF) used for MT may exert adverse effects on MSCs. Thus, we aimed to evaluate the effects of SMF on MSCs in vitro. Cells were initially magnetized using citrate-coated magnetite nanoparticles. Then, control and magnetized MSCs were transferred to an in vitro MT system and exposed to 0.3–0.45 Tesla SMFs. MSC viability, morphology, ultrastructure, proliferation rates, differentiation, and immunomodulation were evaluated after 24 and 48 hours of exposure. MSCs temporarily lost viability and exhibited ultrastructural changes after exposure to SMFs, regardless of magnetization. Moreover, exposure to SMF reduced magnetized MSC proliferation rates. Nevertheless, MSCs remained functional (i.e., capable of differentiating, secreting repair mediators, and modulating alveolar macrophage phenotype). Thus, the experimental protocol tested in this experiment can be applied in future in vivo MT studies.
AB - The magnetic targeting (MT) technique improves delivery of mesenchymal stromal cells (MSCs) to target sites. However, the moderate-intensity static magnetic fields (SMF) used for MT may exert adverse effects on MSCs. Thus, we aimed to evaluate the effects of SMF on MSCs in vitro. Cells were initially magnetized using citrate-coated magnetite nanoparticles. Then, control and magnetized MSCs were transferred to an in vitro MT system and exposed to 0.3–0.45 Tesla SMFs. MSC viability, morphology, ultrastructure, proliferation rates, differentiation, and immunomodulation were evaluated after 24 and 48 hours of exposure. MSCs temporarily lost viability and exhibited ultrastructural changes after exposure to SMFs, regardless of magnetization. Moreover, exposure to SMF reduced magnetized MSC proliferation rates. Nevertheless, MSCs remained functional (i.e., capable of differentiating, secreting repair mediators, and modulating alveolar macrophage phenotype). Thus, the experimental protocol tested in this experiment can be applied in future in vivo MT studies.
KW - Biocompatibility
KW - Cell therapy
KW - Iron oxide nanoparticles
KW - Magnetic targeting
KW - Mesenchymal stromal cells
UR - http://www.scopus.com/inward/record.url?scp=85050166432&partnerID=8YFLogxK
U2 - 10.1016/j.nano.2018.06.002
DO - 10.1016/j.nano.2018.06.002
M3 - Artículo
C2 - 29933023
AN - SCOPUS:85050166432
SN - 1549-9634
VL - 14
SP - 2075
EP - 2085
JO - Nanomedicine: Nanotechnology, Biology, and Medicine
JF - Nanomedicine: Nanotechnology, Biology, and Medicine
IS - 7
ER -