Growth factor-induced FoxO3a nuclear-cytoplasmic pulsing dynamics of non-phosphorylatable reporters in mammary epithelial cell lines. Dataset 1 of 3: single-cell reporter measurements. - Dataset (ID:20290)
|HMS Dataset ID:||20290|
|Dataset Title:||Growth factor-induced FoxO3a nuclear-cytoplasmic pulsing dynamics of non-phosphorylatable reporters in mammary epithelial cell lines. Dataset 1 of 3: single-cell reporter measurements.|
|Screening Lab Investigator:||Somponnat Sampattavanich, Bernhard Steiert|
|Screening Principal Investigator:||Peter K. Sorger|
|Assay Description:||The nuclear-cytoplasmic pulsing behavior of FoxO3a fluorescent reporters (FoxO3aN400-Venus) with or without AKT- and ERK-dependent phosphorylation site mutations was assessed in two mammary epithelial cell lines at the single-cell level using live imaging of cells that were untreated or treated with one of five growth factors.|
1. Cells stably expressing a wild-type FoxO3aN400-HA-Venus-P2A-NLS-Myc-mCherry dual reporter, an ERK-dependent phosphorylation site-mutated FoxO3aN400S294A/S344A-HA-Venus-P2A-NLS-Myc-mCherry dual reporter, or an AKT-dependent phosphorylation site-mutated FoxO3aN400T32A/S253A/S315A-HA-Venus-P2A-NLS-Myc-mCherry dual reporter (in which P2A acts as a self-cleaving peptide between the two reporters in each case) were plated in 96-well plates at ~6 x 105 cells/cm2 and cultured at 37°C with 5% CO2 in DMEM/F12 (Invitrogen) supplemented with 5% horse serum, 20 ng/mL EGF, 10 µg/mL insulin, 0.5 µg/mL hydrocortisone, 100 ng/mL cholera toxin, 50 U/mL penicillin, and 50 µg/mL streptomycin (PMID: 12372298).|
2. Prior to growth factor addition, the cells were washed twice with PBS, placed in serum-free medium (DMEM/F12 with penicillin/streptomycin and no phenol red) for 5 hr, washed again, and placed in fresh serum-free medium.
3. The cells were imaged using a 10x objective on a Nikon Eclipse inverted fluorescence microscope fitted with an environmental chamber maintained at 37°C with 5% CO2. Images were collected at 5 min intervals using a Hamamatsu ORCA-ER cooled CCD camera and Spectra-X light engine (Lumencor).
4. At 75 min, imaging was briefly paused. Growth factor diluted in serum-free medium was added within 1 minute, resulting in an ~5% increase in culture volume, and imaging was resumed and continued for 24 hr.
5. Cell tracking was performed using a custom MATLAB script for cross-correlation between adjacent frames with manual validation. Image segmentation was performed using NLS-Myc-mCherry nuclear reporter signal.
6. Quantification of FoxO3a level in each cell is reported as the mean fluorescent intensity per pixel in the cytosolic region, the mean in the nuclear region, and the log10 ratio of mean cytosolic to nuclear fluorescent intensity (HMS LINCS Dataset #20290).
7. The fPCA harmonics from HMS LINCS Dataset #20287 were used to determine fPC scores for the time interval t = [-70,80] min. These fPC scores represent the projections of the measured data onto the fPCA harmonics.
8. To calculate pulsatile score for times t > 80 min, preprocessing was utilized to bowdlerize artifacts from traces such as spikes resulting from e.g. cell division or loss of tracking. Missing values were added by interpolation. The first three fPCA harmonics of the late response from HMS LINCS Dataset #20287 were employed to remove the large time scales. Peaks were detected on the smooth data representation. Due to overfitting, the pulsatile traces are mixed with small artificial peaks. These were dropped if the peaks were smaller than a certain threshold. The final detrended, interpolated, and peak-adjusted signals were then lumped into the following features fi:
(1) number of edges (approximately 2x the number of peaks)
(2) range (min-to-max)
(3) signal-to-noise ratio = range/(1/(N-1)*sqrt(RSS)) with RSS = distance of spline to data
(4) peak duration = mean(edge_start to neighboring_edge_end)
(5) peak distance = mean(min to neighboring min; max to neighboring max)
Whenever no peaks were detected, peak duration and peak distance were set to 300 min. A reference value ri and a weight wi were defined for all features fi. A positive value for wi was chosen for features where a larger number represents more pulsing, i.e. nEdges, range, and signal-to-noise ratio. A negative number for wi was assigned to features where a larger number indicates less pulsing, i.e. peak duration and distance. Using the features fi, the reference values ri, and the weights wi, pulsatile score
was calculated and compared to a threshold for assigning each trace into either the pulsing or the non-pulsing group (HMS LINCS Dataset #20291).
9. Finally, mean fPCA values and features were calculated across all single-cell traces for a given condition, and the fraction of pulsing cells per condition
was calculated (HMS LINCS Dataset #20292).
10. The complete set of images for this dataset is viewable online through our OMERO server at omero.hms.harvard.edu/webclient/?show=plate-704, and a lookup table with data file data column definitions is contained within the downloadable data package for this dataset.
|HMS Dataset Type:||Microscopy/Imaging|
|Date Publicly Available:||2017-05-02|
|Most Recent Update:||2017-05-02|