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Introduction

To test receptor activation in a natural context, it was also tried to activate T-cells (B12.7.5) with the NIP-linked DNA-origami. Those T-cells have a NIP Fab-fragment genetically fused to their receptor. During these tests many problems were faced which could emerge as obstacles in the main project, the artificial receptor, which is expressed by 293T-cells.
One problem was to find a medium in which the T-cells survive, the DNA-Origami structures are stable and which is also suitable for the fluorescent measurement on the microsop). Normally, the cells were kept in RPMI (10% FCS), but the phenol red itself is an electron acceptor and would disturb the measurement. Another complication was, that the Origami need a high Mg2+ concentration (12,5 mM), which stabilizes the DNA backbone, but low concentration of other bivalent cations, which could disrupt the Origami. None of the common cell culture medium does achieve these conditions. In order to solve the cell culture problem the stability of the Origami in different media were tested (see DNA-Origami). On the other hand we also had to test if our cells survive 12,5 mM Mg2+, which we tested with an MTT-Assay.
As explained before, we also wanted to use the Origami to activate T-cell receptors (TCR) by clustering. For this experiment we measured the calcium influx with a FACS, as described earlier (Susana Minguet, Immunity Vol. 26, Page 43-54). But in this publication much higher concentration of the stimulus were used than we were able to produce. Therefore we were looking for another method to measure the calcium influx. One very commonly used method is to stain the cells with Fura-2AM and measure the changes in calcium concentration with a confocal laser scanning microscope. Usually this measurement is only suitable for adherent cells, because by giving the stimulus to the cells the cells would move. To avoid this problem we used Poly-L-Lysin coated µ-Slides(ibidi).
To check, that the DNA-Origami really bind specifically to the cells(T-cells and B-cells), Alexa 488 linked origamis with and without NIP were given to the cells and the fluorescence was visualized with a LSM.

Material and Methods

Cell stability in the presence of Mg2+ measured by MTT-Assay

To test the Mg2+ tolerance of the T-cells (cell line B.12.7.5), 100 µl cellsuspension was mixed with 800 µl RPMI medium  and 100 µl  MgCl2 or MgAc, respectively containing various concentrations of Mg2+ in a 24-well plate. 3 days later cells of each well were spun down, the supernatant was discarded and the cells were resuspended in 200 µl new RPMI medium. 50 µl 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromid (MTT) was added to each sample. After 4 h of incubation at 37°C the cells were spun down again and after discarding the medium the pellet was resolved in 400 µl DMSO and 50 µl Soerensens’ reagent. The reduced blue MTT was detected in a photometer at 570nm.

B-cells (cell line j558lδmmb1nfleck)  from 10ml dishes were spun down and resuspended in 9ml Krebs-Ringer-Hepes (12,5mM MgAc). After incubation for 45min the cells were spun down again and resolved in 1ml PBS. 5µl of the suspension was mixed with 45µl Trypan blue and the cells were counted in a “Neubauer cell chamber”.

Media

Medium for B- and T-cell :

• RPMI
• 10%FCS 
• HEPES (10mM) 
• β-mercaptoethanol (50µM) 
• L-Glutamine (2mM)
• 1%Pen-Strep

Medium for 293T:

• DMEM
• 10% FCS 
• 5% PenStrep 
• L-Glutamine (1,5mM)
  

Krebs-Ringer-Hepes (12.5mM):

• NaCl (155 mM)
• KCl (4.5 mM)
• CaCl2 (2 mM)
• MgCl2 (1 mM)
• MgAcetat (11.5mM)
• D-glucose (10 mM)
• Hepes (5 mM)

->  pH 7.4 with NaOH

Binding measurement

To test the binding between origamis and T-cells/B-cells 15µl cell suspension in Ringer (12,5mM Mg2+) or TA-buffer (12,5mM Mg2+) was mixed with 15µl of origamis on a µ-Slide (ibidi, µ-Slides 18 well-flat, Cat. No: 81824). Those slides are coated with Poly-L-Lysine, which fixes the cells on the bottom of the slide. So the suspensions cells could be measured on a microscope.

Calcium2+ measurement

Ca2+ measurement with microscope

By binding of ligands to a receptor at the cell surface the cell reacts amongst others with a efflux of calciumions from the ER into the cytoplasm. To measure the intensity of activation one way is to quantify the concentration or rather the increase of calciumions in the cytoplasm. Fura-2 is a fluorescent dye which change the quality dependent on the Ca2+ concentration. Fura-2AM (Fura-2-acetoxymethyl ester) is a membrane-permeable derivative of Fura-2 but after crossing the membrane the acetoxymethyl groups are removed by cellular esterases so it remains as Fura-2 in the cytoplasm. Fura-2 is excited at 340 nm and 380 nm of light, and the ratio of the emissions at those wavelengths is directly correlated to the amount of intracellular calcium. Without Ca2+ the maximum emission results from excitation at 365nm. With Ca2+ the maximum emission change to excitation at 340nm and the emission decrease by extinction at 380nm.
So to measure properly it is necessary to alternate quickly between the two excitation wavelengths. Excitation was measured with a high-end inverted fluorescenc microscope (Zeiss Axiovert 100).
       
   

Fig. 1: Fura-2 Emission with (blue) and without free calciumions (red)

Ca2+ measurement with FACS

Cells resuspended in medium with 1% serum were incubated with 5 μg/ml of Indo-1, which is the Ca2+ complexing dye,  and 0.5 μg/ml of pluronic F-127, which fasilitates dye uptake (both Molecular Probes) 45 min at 37°C. After incubation, cells were distributed into to 1.5ml eppendorf tubes and the washed with the medium we wanted to measure them. After washing, cells were resuspended in the according medium and kept on ice. Ca2+ response was induced by addition of the indicated stimulus 1 min after starting to record the ratio of Ca2+-bound Indo-1 versus unbound Indo-1 with a LSRII fluorescence spectrometer (Becton Dickinson). Cells were measured for approximately 2min before putting the stimuli on it. Data were analyzed with the FloJo 6.1 software.

Results and discussion

Cell stability in the presence of Mg2+ measured by MTT-Assay

B-cells:
Counting stained and unstained B-cells brought following result:
Dead cells : 1
Living cells: 44
Total cell number: 45

293T-cells:
The MTT assays and the trypan blue staining proofed the tolerance of the used cells towards a concentration up to 12,5mM Mg2+. This is the exact concentration in which the origami are produced and stored. The lower absorbance in the tests with TA could possibly come from the removal of the TA-buffer because it seemed that the TA buffer disturbs the adhesion of the 293T cells to the ground of the well so that some cells might be sucked off with the TA.

Calcium2+ measurement

Ca2+ measurement with FACS

In this measurement we tried to activate T-Cells by clustering. Therefore we tested two different buffers, Krebs-Ringer-Hepes with 12,5mM Mg2+ buffer and TA with 12,5mM Mg2+. As positive control we used UCHT1 (=anti-CD3), which can stimulate T-cells (Susana Minguet, Vol. 26, Page 43-54).

 
Fig. X: Results of the FACS measurement. Cells were stained with Indo-1. Different stimuli were used. Stimuli were given after 1min. Time is given in seconds. Green line: cells buffered in Krebs-Ringer-Hepes buffer. The both other lines show the positive controls of cells buffered in TA (blue) and Krebs-Ringer-Hepes (red).

Figure X shows the change in intra cellular calcium concentration after adding the DNA-Origami (green) compared to the positive controls (blue and red). The cells in Krebs-Ringer-Hepes buffer, which were stimulated with UCHT 1 show a very high activation, while the cells buffered in TA and the Origami treaded cell show only a slowly signal. When we put the cells buffered in TA in the LSRII fluorescence spectrometer and rechecked all the settings we saw, that most of the cells were already dead. This could be the reason for the low signal of the TA buffered cells (blue line). The cells treaded with Origami didn´t show any calcium change at all. After the FACS measurement we tested some of those Origami on the AFM. None of the Origami which we used were stable, so probably that is the reason why we couldn´t see any signal by adding NIP-Origami. To affirm this conclusion this measurement would have to be carried out again.

Ca2+ measurement with microscope

This measurement was also used to activate the T-cell receptors (TCR) by clustering. The TCR's were modified with a anti-NIP antibodies and the NIP-molecules were coupled to DNA origamis. As a negative control we used a DNA-Origami without NIP. The positive control was Pervanadat.
By adding the origamis to the cells we could see a small signal for both with and without NIP. The amount of fluorescent cells increase slowly but there was no significant difference between the negative control and the sample (7 NIP's per origami).
By contrast the Pervanadat produced a strong signal that differs from the origami reactions.



In contrast to the positive control Pervanadat which was working quit well, our sample (DNA-origami with NIP) and the negative control (DNA-origami without NIP) did not show a significant Ca2+ efflux. There are two reasons which could be responsible that the cell answer to origamis with and without NIP’s almost looks the same.
1. Spatial avoidance: Because of the rough surface of T-cells big molecules could have problems to trigger two or more TCR’s. Also huge extracellular proteins could avoid that the nanoplates reach the small TCR’s.
2. Non-specific binding:
Also the negative control produced a weak signal which could result from non-specific binding to the cell surface, because the cells were not blocked.

In both cases the slow Ca2+ efflux could result from the mechanical touch between the cells by adding the liquid with the probes.

Binding measurement

During the binding measurements it seemed that the origamis were absorbed by the cells or that they bind unspecifically. Later tests at the AFM showed no functional origami which could be an explanation to the behaviour of the cells. The expanded form of the B-cells in TA-buffer showed that sole TA-buffer is osmotically disadvantageous for the cells.