The effect of lance geometry and carbon coating of silicon lances on propidium iodide uptake in lance array nanoinjection of HeLa 229 cells

2016 ◽  
Vol 26 (4) ◽  
pp. 045002
Author(s):  
John W Sessions ◽  
Dallin L Lindstrom ◽  
Brad W Hanks ◽  
Sandra Hope ◽  
Brian D Jensen
Author(s):  
John W. Sessions ◽  
Brad W. Hanks ◽  
Dallin L. Lindstrom ◽  
Sandra Hope ◽  
Brian D. Jensen

Understanding environmental factors relative to transfection protocols is key for improving genetic engineering outcomes. In the following work, the effects of temperature on a nonviral transfection procedure previously described as lance array nanoinjection are examined in context of molecular delivery of propidium iodide (PI), a cell membrane impermeable nucleic acid dye, to HeLa 229 cells. For treatment samples, variables include varying the temperature of the injection solution (3C and 23C) and the magnitude of the pulsed voltage used during lance insertion into the cells (+5 V and +7 V). Results indicate that PI is delivered at levels significantly higher for samples injected at 3C as opposed to 23C at four different postinjection intervals (t = 0, 3, 6, 9 mins; p-value ≤ 0.005), reaching a maximum value of 8.3 times the positive control for 3 C/7 V pulsed samples. Suggested in this work is that between 3 and 6 mins postinjection, a large number of induced pores from the injection event close. While residual levels of PI still continue to enter the treatment samples after 6 mins, it occurs at decreased levels, suggesting from a physiological perspective that many lance array nanoinjection (LAN) induced pores have closed, some are still present.


Author(s):  
Zachary K. Lindstrom ◽  
Nicholas Gregory ◽  
Brian D. Jensen

An automated nanoinjection system has been developed and tested for the delivery of propidium iodide into culture cells. Nanoinjection is the process by which molecules are delivered into living cells using a solid needle. Propidium iodide, a dye that fluoresces when bound to nucleic acids, was used as the injection molecule to monitor nanoinjection efficiency. The nanoinjection system uses a programmable microcontroller to manipulate a linear actuator, which presses a silicon lance array into thousands of living culture cells simultaneously. The lances penetrate cell membranes, allowing dye molecules to enter the cell through membrane pores opened by lances. The system was developed to apply the same injection force to each cell sample at the press of a button, eliminating any experimental variability in data due to the operator. Tests were performed at a dye concentration of 0.04 mg/mL for all experiments. Several forces were tested to determine the optimal nanoinjection force needed for maximum dye delivery. We found the optimal force range to be 8.8–14.7 N. The average PI uptake into cells at a force of 8.8 N and 14.7 N is 57.6±7.7% and 60.3±6.6%, respectively. Previous studies with a manual injection force have shown average propidium iodide uptake to be 60.4±18.0%. High cell viability is maintained with the automated nanoinjection system. At all forces applied in this experiment, an average of 78% or greater viability was observed. With the data gathered in this experiment, we conclude that the automated nanoinjection system eliminates much of the uptake efficiency variability inherent to nanoinjections performed with a manual injection force.


2016 ◽  
Vol 2016 (11) ◽  
pp. pdb.prot087288 ◽  
Author(s):  
Lisa C. Crowley ◽  
Brooke J. Marfell ◽  
Adrian P. Scott ◽  
Nigel J. Waterhouse

1999 ◽  
Vol 67 (5) ◽  
pp. 2575-2584 ◽  
Author(s):  
John K. Crane ◽  
Swastika Majumdar ◽  
Donald F. Pickhardt

ABSTRACT Enteropathogenic Escherichia coli (EPEC) is a cause of prolonged watery diarrhea in children in developing countries. The ability of EPEC to kill host cells was investigated in vitro in assays using two human cultured cell lines, HeLa (cervical) and T84 (colonic). EPEC killed epithelial cells as assessed by permeability to the vital dyes trypan blue and propidium iodide. In addition, EPEC triggered changes in the host cell, suggesting apoptosis as the mode of death; such changes included early expression of phosphatidylserine on the host cell surface and internucleosomal cleavage of host cell DNA. Genistein, an inhibitor of tyrosine kinases, and wortmannin, an inhibitor of host phosphatidylinositol 3-kinase, markedly increased EPEC-induced cell death and enhanced the features of apoptosis. EPEC-induced cell death was contact dependent and required adherence of live bacteria to the host cell. A quantitative assay for EPEC-induced cell death was developed by using the propidium iodide uptake method adapted to a fluorescence plate reader. With EPEC, the rate and extent of host cell death were less that what has been reported forSalmonella, Shigella, and Yersinia, three other genera of enteric bacteria known to cause apoptosis. However, rapid apoptosis of the host cell may not favor the pathogenic strategy of EPEC, a mucosa-adhering, noninvasive pathogen.


Author(s):  
John W. Sessions ◽  
Brad W. Hanks ◽  
Tyler E. Lewis ◽  
Brian D. Jensen ◽  
Dallin L. Lindstrom ◽  
...  

Being able to deliver molecular loads to the intracellular space of mammalian cells is a key initial step of genetic engineering. In the following work, experimentation with nanoinjection, a non-viral molecular load delivery technique, was examined in regards to transmembrane delivery of propidium iodide (PI), a dye that cannot penetrate the cell membrane and fluoresces when bound to genetic material. Investigation includes two environmental factors: peak pulse amplitude (1.5 to 3, 5, 7, or 9 V) and saline type (HBSS, PBS with potassium, and PBS without potassium). Results indicate that PBS with potassium has significantly higher PI uptake efficiency than the other two saline solutions for pulsed voltages of 3V, 5V, and 7V (with the peak value being 3.352 times greater than the positive control). Also, cell viability analysis indicates that there is a measureable reduction in cell viability for voltage protocol samples in comparison to non-voltage protocol samples. Cell viabilities range from 74.5% to 89.4% for voltage protocol samples. Findings suggest that a possible combination of physical/electrical variables work in concert with biological mechanisms to contribute to overall cell survival and PI uptake efficiency in nanoinjection.


1999 ◽  
Vol 43 (4) ◽  
pp. 830-835 ◽  
Author(s):  
Lisa J. Green ◽  
Philip Marder ◽  
Larry L. Mann ◽  
Li-Chun Chio ◽  
William L. Current

ABSTRACT LY303366 is a semisynthetic analog of the antifungal lipopeptide echinocandin B that inhibits (1,3)-β-d-glucan synthase and exhibits efficacy in animal models of human fungal infections. In this study, we utilized flow cytometric analysis of propidium iodide uptake, single-cell sorting, and standard microbiological plating methods to study the antifungal effect of LY303366 on Saccharomyces cerevisiae and Candida albicans. Our data indicate that an initial 5-min pulse treatment with LY303366 caused yeasts to take up propidium iodide and lose their ability to grow. Amphotericin B and cilofungin required longer exposure periods (30 and 180 min, respectively) and higher concentrations to elicit these fungicidal effects. These two measurements of fungicidal activity by LY303366 were highly correlated (r > 0.99) in concentration response and time course experiments. As further validation, LY303366-treated yeasts that stained with propidium iodide were unable to grow in single-cell-sorted cultures. Our data indicate that LY303366 is potent and rapidly fungicidal for actively growing yeasts. The potency and rapid action of this new fungicidal compound suggest that LY303366 may be useful for antifungal therapy.


1993 ◽  
Vol 100 (3) ◽  
pp. 223-229 ◽  
Author(s):  
Marco Vitale ◽  
Loris Zamai ◽  
Giovanni Mazzotti ◽  
Amelia Cataldi ◽  
Elisabetta Falcieri

2008 ◽  
Vol 58 (1) ◽  
pp. 56-62 ◽  
Author(s):  
M. S. Gião ◽  
S. A. Wilks ◽  
N. F. Azevedo ◽  
M. J. Vieira ◽  
C. W. Keevil

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