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Difference between revisions of "Orynbayeva 2015 Nanomedicine (Lond)"

From Bioblast
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|year=2015
|year=2015
|journal=Nanomedicine (Lond)
|journal=Nanomedicine (Lond)
|abstract=To successfully translate magnetically mediated cell targeting from bench to bedside, there is a need to systematically assess the potential adverse effects of magnetic nanoparticles (MNPs) interacting with 'therapeutic' cells. Here, we examined in detail the effects of internalized polymeric MNPs on primary rat endothelial cells' structural intactness, metabolic integrity and proliferation potential.
|abstract=Aim: To successfully translate magnetically mediated cell targeting from bench to bedside, there is a need to systematically assess the potential adverse effects of magnetic nanoparticles (MNPs) interacting with ‘therapeutic’ cells. Here, we examined in detail the effects of internalized polymeric MNPs on primary rat endothelial cells’ structural intactness, metabolic integrity and proliferation potential.


The intactness of cytoskeleton and organelles was studied by fluorescent confocal microscopy, flow cytometry and high-resolution respirometry.
Materials & methods: The intactness of cytoskeleton and organelles was studied by fluorescent
confocal microscopy, flow cytometry and high-resolution respirometry. Results: MNPloaded primary endothelial cells preserve intact cytoskeleton and organelles, maintain normal rate of proliferation, calcium signaling and mitochondria energy metabolism.


MNP-loaded primary endothelial cells preserve intact cytoskeleton and organelles, maintain normal rate of proliferation, calcium signaling and mitochondria energy metabolism.
Conclusion: This study provides supportive evidence that MNPs at doses necessary
 
for targeting did not induce significant adverse effects on structural integrity and functionality of primary endothelial cells potential cell therapy vectors.
This study provides supportive evidence that MNPs at doses necessary for targeting did not induce significant adverse effects on structural integrity and functionality of primary endothelial cells - potential cell therapy vectors.
|keywords=Ca2+ signaling, Cytoskeleton, Magnetic nanoparticles, Mitochondria membrane potential, Mitochondria oxidative phosphorylation, Primary endothelial cells
|keywords=Ca2+ signaling, Cytoskeleton, Magnetic nanoparticles, Mitochondria membrane potential, Mitochondria oxidative phosphorylation, Primary endothelial cells
|mipnetlab=US PA Philadelphia Orynbayeva Z
}}
}}
{{Labeling
{{Labeling
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|preparations=Intact cells
|preparations=Intact cells
|couplingstates=LEAK, ROUTINE, ETS
|couplingstates=LEAK, ROUTINE, ETS
|substratestates=CI, ROX
|substratestates=ROX
|instruments=Oxygraph-2k
|instruments=Oxygraph-2k
|additional=Labels
}}
}}

Revision as of 12:53, 13 October 2015

Publications in the MiPMap
Orynbayeva Z, Sensenig R, Polyak B (2015) Metabolic and structural integrity of magnetic nanoparticle-loaded primary endothelial cells for targeted cell therapy. Nanomedicine (Lond) 10:1555-68.

» PMID: 26008193

Orynbayeva Z, Sensenig R, Polyak B (2015) Nanomedicine (Lond)

Abstract: Aim: To successfully translate magnetically mediated cell targeting from bench to bedside, there is a need to systematically assess the potential adverse effects of magnetic nanoparticles (MNPs) interacting with ‘therapeutic’ cells. Here, we examined in detail the effects of internalized polymeric MNPs on primary rat endothelial cells’ structural intactness, metabolic integrity and proliferation potential.

Materials & methods: The intactness of cytoskeleton and organelles was studied by fluorescent confocal microscopy, flow cytometry and high-resolution respirometry. Results: MNPloaded primary endothelial cells preserve intact cytoskeleton and organelles, maintain normal rate of proliferation, calcium signaling and mitochondria energy metabolism.

Conclusion: This study provides supportive evidence that MNPs at doses necessary for targeting did not induce significant adverse effects on structural integrity and functionality of primary endothelial cells – potential cell therapy vectors. Keywords: Ca2+ signaling, Cytoskeleton, Magnetic nanoparticles, Mitochondria membrane potential, Mitochondria oxidative phosphorylation, Primary endothelial cells

O2k-Network Lab: US PA Philadelphia Orynbayeva Z


Labels: MiParea: Respiration, mt-Membrane 


Organism: Rat  Tissue;cell: Endothelial;epithelial;mesothelial cell  Preparation: Intact cells 


Coupling state: LEAK, ROUTINE, ETS"ETS" is not in the list (LEAK, ROUTINE, OXPHOS, ET) of allowed values for the "Coupling states" property. 

HRR: Oxygraph-2k