scholarly journals Rapid Magnetic 3D Printing of Cellular Structures with MCF-7 Cell Inks

Research ◽  
2019 ◽  
Vol 2019 ◽  
pp. 1-13 ◽  
Author(s):  
S. Mishriki ◽  
A. R. Abdel Fattah ◽  
T. Kammann ◽  
R. P. Sahu ◽  
F. Geng ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Magnetic Field Gradient ◽  
Cell Monolayer ◽  
Hypoxia Inducible Factor ◽  
Label Free ◽  
3D Scaffold ◽  
Gene Expressions ◽  
3D Structures ◽  
Paramagnetic Salt ◽  
Mcf 7

A contactless label-free method using a diamagnetophoretic ink to rapidly print three-dimensional (3D) scaffold-free multicellular structures is described. The inks consist of MCF-7 cells that are suspended in a culture medium to which a paramagnetic salt, diethylenetriaminepentaacetic acid gadolinium (III) dihydrogen salt hydrate (Gd-DTPA), is added. When a magnetic field is applied, the host fluid containing the paramagnetic salt is attracted towards regions of high magnetic field gradient, displacing the ink towards regions with a low gradient. Using this method, 3D structures are printed on ultra-low attachment (ULA) surfaces. On a tissue culture treated (TCT) surface, a 3D printed spheroid coexists with a two-dimensional (2D) cell monolayer, where the composite is termed as a 2.5D structure. The 3D structures can be magnetically printed within 6 hours in a medium containing 25 mM Gd-DTPA. The influence of the paramagnetic salt on MCF-7 cell viability, cell morphology, and ability of cells to adhere to each other to stabilize the printed structures on both ULA and TCT surfaces is investigated. Gene expressions of hypoxia-inducible factor 1-alpha (HIF1α) and vascular endothelial growth factor (VEGF) allow comparison of the relative stresses for the printed 3D and 2.5D cell geometries with those for 3D spheroids formed without magnetic assistance. This magnetic printing method can be potentially scaled to a higher throughput to rapidly print cells into 3D heterogeneous cell structures with variable geometries with repeatable dimensions for applications such as tissue engineering and tumour formation for drug discovery.

scholarly journals Rapid Magnetic 3D Printing of Cellular Structures with MCF-7 Cell Inks

Research ◽  
2019 ◽  
Vol 2019 ◽  
pp. 1-13 ◽  
Author(s):  
S. Mishriki ◽  
A. R. Abdel Fattah ◽  
T. Kammann ◽  
R. P. Sahu ◽  
F. Geng ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Magnetic Field Gradient ◽  
Cell Monolayer ◽  
Hypoxia Inducible Factor ◽  
Label Free ◽  
3D Scaffold ◽  
Gene Expressions ◽  
3D Structures ◽  
Paramagnetic Salt ◽  
Mcf 7

A contactless label-free method using a diamagnetophoretic ink to rapidly print three-dimensional (3D) scaffold-free multicellular structures is described. The inks consist of MCF-7 cells that are suspended in a culture medium to which a paramagnetic salt, diethylenetriaminepentaacetic acid gadolinium (III) dihydrogen salt hydrate (Gd-DTPA), is added. When a magnetic field is applied, the host fluid containing the paramagnetic salt is attracted towards regions of high magnetic field gradient, displacing the ink towards regions with a low gradient. Using this method, 3D structures are printed on ultra-low attachment (ULA) surfaces. On a tissue culture treated (TCT) surface, a 3D printed spheroid coexists with a two-dimensional (2D) cell monolayer, where the composite is termed as a 2.5D structure. The 3D structures can be magnetically printed within 6 hours in a medium containing 25 mM Gd-DTPA. The influence of the paramagnetic salt on MCF-7 cell viability, cell morphology, and ability of cells to adhere to each other to stabilize the printed structures on both ULA and TCT surfaces is investigated. Gene expressions of hypoxia-inducible factor 1-alpha (HIF1α) and vascular endothelial growth factor (VEGF) allow comparison of the relative stresses for the printed 3D and 2.5D cell geometries with those for 3D spheroids formed without magnetic assistance. This magnetic printing method can be potentially scaled to a higher throughput to rapidly print cells into 3D heterogeneous cell structures with variable geometries with repeatable dimensions for applications such as tissue engineering and tumour formation for drug discovery.

Spectroscopic imaging of human disease

1996 ◽  
Vol 54 ◽  
pp. 884-885
Author(s):  
D.J. Meyerhoff
Keyword(s):  
Magnetic Field ◽  
Magnetic Resonance ◽  
Field Gradient ◽  
Human Disease ◽  
Morphological Changes ◽  
Magnetic Field Gradient ◽  
Spectroscopic Imaging ◽  
Resonance Spectroscopy ◽  
Tissue Water

Magnetic Resonance Imaging (MRI) observes tissue water in the presence of a magnetic field gradient to study morphological changes such as tissue volume loss and signal hyperintensities in human disease. These changes are mostly non-specific and do not appear to be correlated with the range of severity of a certain disease. In contrast, Magnetic Resonance Spectroscopy (MRS), which measures many different chemicals and tissue metabolites in the millimolar concentration range in the absence of a magnetic field gradient, has been shown to reveal characteristic metabolite patterns which are often correlated with the severity of a disease. In-vivo MRS studies are performed on widely available MRI scanners without any “sample preparation” or invasive procedures and are therefore widely used in clinical research. Hydrogen (H) MRS and MR Spectroscopic Imaging (MRSI, conceptionally a combination of MRI and MRS) measure N-acetylaspartate (a putative marker of neurons), creatine-containing metabolites (involved in energy processes in the cell), choline-containing metabolites (involved in membrane metabolism and, possibly, inflammatory processes),

Simple Systems

2017 ◽  
Author(s):  
Jochen Rau
Keyword(s):  
Magnetic Field ◽  
Low Temperatures ◽  
General Framework ◽  
Gibbs State ◽  
Macroscopic System ◽  
Basic Model ◽  
System A ◽  
Paramagnetic Salt ◽  
High And Low Temperatures ◽  
Simple Systems

Even though the general framework of statistical mechanics is ultimately targeted at the description of macroscopic systems, it is illustrative to apply it first to some simple systems: a harmonic oscillator, a rotor, and a spin in a magnetic field. These applications serve to illustrate how a key function associated with the Gibbs state, the so-called partition function, is calculated in practice, how the entropy function is obtained via a Legendre transformation, and how such systems behave in the limits of high and low temperatures. After discussing these simple systems, this chapter considers a first example where multiple constituents are assembled into a macroscopic system: a basic model of a paramagnetic salt. It also investigates the size of energy fluctuations and how—in the case of the paramagnet—these fluctuations scale with the number of constituents.

scholarly journals Magnetic hybrid materials interact with biological matrices

2020 ◽  
Vol 0 (0) ◽  
Author(s):  
Christine Gräfe ◽  
Elena K. Müller ◽  
Lennart Gresing ◽  
Andreas Weidner ◽  
Patricia Radon ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Field Gradient ◽  
Hybrid Materials ◽  
Biomedical Application ◽  
Magnetic Field Gradient ◽  
Apical Cell ◽  
Cell Type ◽  
Cell Layers ◽  
Barrier Model

Abstract Magnetic hybrid materials are a promising group of substances. Their interaction with matrices is challenging with regard to the underlying physical and chemical mechanisms. But thinking matrices as biological membranes or even structured cell layers they become interesting with regard to potential biomedical applications. Therefore, we established in vitro blood-organ barrier models to study the interaction and processing of superparamagnetic iron oxide nanoparticles (SPIONs) with these cellular structures in the presence of a magnetic field gradient. A one-cell-type–based blood-brain barrier model was used to investigate the attachment and uptake mechanisms of differentially charged magnetic hybrid materials. Inhibition of clathrin-dependent endocytosis and F-actin depolymerization led to a dramatic reduction of cellular uptake. Furthermore, the subsequent transportation of SPIONs through the barrier and the ability to detect these particles was of interest. Negatively charged SPIONs could be detected behind the barrier as well as in a reporter cell line. These observations could be confirmed with a two-cell-type–based blood-placenta barrier model. While positively charged SPIONs heavily interact with the apical cell layer, neutrally charged SPIONs showed a retarded interaction behavior. Behind the blood-placenta barrier, negatively charged SPIONs could be clearly detected. Finally, the transfer of the in vitro blood-placenta model in a microfluidic biochip allows the integration of shear stress into the system. Even without particle accumulation in a magnetic field gradient, the negatively charged SPIONs were detectable behind the barrier. In conclusion, in vitro blood-organ barrier models allow the broad investigation of magnetic hybrid materials with regard to biocompatibility, cell interaction, and transfer through cell layers on their way to biomedical application.

Two-dimensional EPR imaging with the rapid scan and rotated magnetic field gradient

2014 ◽  
Vol 248 ◽  
pp. 126-130 ◽  
Author(s):  
T. Czechowski ◽  
W. Chlewicki ◽  
M. Baranowski ◽  
K. Jurga ◽  
P. Szczepanik ◽  
...  
Keyword(s):  
Magnetic Field ◽  
Field Gradient ◽  
Magnetic Field Gradient ◽  
Two Dimensional ◽  
Rapid Scan

scholarly journals Direct mechanical stimulation of tip links in hair cells through DNA tethers

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
Aakash Basu ◽  
Samuel Lagier ◽  
Maria Vologodskaia ◽  
Brian A Fabella ◽  
AJ Hudspeth
Keyword(s):  
Magnetic Field ◽  
Field Gradient ◽  
Mechanical Stimulation ◽  
Hair Cells ◽  
Magnetic Field Gradient ◽  
Hair Bundle ◽  
Mechanical Forces ◽  
Mechanoelectrical Transduction ◽  
Superparamagnetic Beads ◽  
Stimulation Of

Mechanoelectrical transduction by hair cells commences with hair-bundle deflection, which is postulated to tense filamentous tip links connected to transduction channels. Because direct mechanical stimulation of tip links has not been experimentally possible, this hypothesis has not been tested. We have engineered DNA tethers that link superparamagnetic beads to tip links and exert mechanical forces on the links when exposed to a magnetic-field gradient. By pulling directly on tip links of the bullfrog's sacculus we have evoked transduction currents from hair cells, confirming the hypothesis that tension in the tip links opens transduction channels. This demonstration of direct mechanical access to tip links additionally lays a foundation for experiments probing the mechanics of individual channels.

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