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1 1 © 2009 PerkinElmer
Brad N. Taylor, Ph.D.
Advanced Imaging Training Manager
Spectrum CT 202 Advanced Imaging of Fluorescent and Bioluminescent Probes
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2 2
10:00 – 12:00 AM Presentation – Advanced Imaging of Fluorescent and Bioluminescent Probes
IVIS Spectrum and Living Image Software
Imaging Concepts
Optical Imaging Workflow and Experimental Design
Advanced Fluorescence – Epi vs. Transillumination and Spectral Unmixing
3D Tomography
12:00 – 1:00 PM Lunch
1:00 – 5:00 PM Hands on with Phantom Mice
Basic Acquisition Overview with focus on BLI
Tool Palette In-depth
Bioluminescence Tomography
9:00 – 12:00 PM Hands on with Phantom Mice
Fluorescence Acquisition
Spectral Unmixing
Transillumination with Fluorescence Tomography
12:00 – End Wrap up – Live animal imaging if provided
Introduction
Training Schedule
Day 1
Day 2
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3 3 Introduction
Why Optical In Vivo Imaging?
Shcherbakova, DM.. Nat. Met. 2013
Brighter signal
Multitude of reporters
Translational
Ease of use
Unmatched sensitivity
Highest Signal:Noise
Easiest analysis
Bioluminescence features Fluorescence features
Wide range of applications
Useful for functional imaging and tracer applications
Reduce number of animals
Simple instrumentation, interface, and integration into current workflow
Amount of light is proportional to number of copies of the gene or amount of fluorescent probe
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5 5
High sensitivity CCD for bioluminescence or fluorescence imaging
High throughput (23 cm) or high resolution FOV
28 discrete bandpass filters 490 – 850 nm
Monochromatic imaging or spectral unmixing
Reflection (Epi-) or transmission-mode fluorescence
3D optical tomographic reconstructions for both bioluminescence
and fluorescence
Ideal for imaging multiple probes/reporters
Low-dose mCT x-ray exposure for longitudinal studies
High resolution, smaller field of view mCT for detailed analysis
Introduction
IVIS® Spectrum CT
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6 6
Controls all settings in the IVIS® system (fully computer
controlled)
Advanced cataloging and browsing tools
Analysis tools for quantification
Instrument settings are analogous to photography
User-friendly interface
Imaging Wizard assists in choosing optimal setup and
analysis parameters
Auto-exposure for optimal image capture settings
microCT acquisition setup and reconstruction is simplified
and optimized for ease-of-use Introduction
Living Image® Software
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7 7
Camera and Lens Settings are Analogous to Photography
Field of View (FOV) is
dependent on the distance from
the lens to the sample
Light collected is proportional to
how long the shutter is open
(exposure time)
Aperture (ƒ/stop) controls the
amount of light collected
Digital pixel binning is possible
on the CCD – alters
sensitivity/resolution
Basic Imaging Concepts
Aperture (f/stop)
Shutter CCD
Field of View
Emission Filters
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8 8
Setting Sensitivity – Signal Level
The IVIS® CCD camera has a raw signal range of 0 to 65,535 Analog to Digital counts (216 or
16-bit)
Adjust camera settings to obtain a signal level of 600 to 60,000 counts
Settings that control signal level are:
Exposure time
Pixel binning (CCD resolution)
ƒ/stop (aperture)
Instrument is calibrated to automatically compensate for changes in sensitivity settings
Basic Imaging Concepts
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9 9
Exposure Time
Signal level is directly proportional to exposure
time (1:1)
Shorter exposure time improves throughput
Recommended minimum exposure time > 0.5
seconds
Longer exposure times increase signal intensity
Recommended maximum exposure time < 5
minutes
Basic Imaging Concepts
2 sec f/1 small binning
~5000 counts peak
10 sec f/1 small binning
~25000 counts peak
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10 10
ƒ/stop (Lens Aperture)
ƒ/stop controls the amount of light
received by the CCD detector
ƒ/1 is wide open, maximum light
collection – default for luminescent
ƒ/8 is smallest aperture, best resolution
– default for photo
Changing f/stop changes counts by a
factor of 4
Basic Imaging Concepts
ƒ/1 ƒ/8
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11 11
Pixel Binning (CCD Resolution)
Binning refers to the grouping of pixels into a larger super-pixel
Changing binning settings changes counts by a factor of 4
Basic Imaging Concepts
10 seconds f/2 Large Binning
10 seconds f/2 Medium Binning
10 seconds f/2 Small Binning
• Large Binning (16 x 16)
Higher Sensitivity/Lower Resolution
• Medium Binning (8 x 8)
Default
• Small Binning (4 x 4)
Lower Sensitivity/Higher Resolution
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12 12
Calibrated Physical Units
Living Image® automatically compensates for device settings: Exposure time, ƒ/stop, binning
and field of view.
Calibrated unit is Radiance, representing the flux radiating omni-directionally from a user-
defined region
Basic Imaging Concepts
2 sec exposure, f/stop 1, Small binning ~5000 counts peak
2.82 x 108 photons/sec
10 sec exposure, f/stop 1, Small binning ~25000 counts peak
2.82 x 108 photons/sec
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13 13
Calibrated Physical Units vs. Raw Signal
Basic Imaging Concepts
Raw Signal (Counts)
Exp time: 30 sec 30 sec 60 sec 60 sec 60 sec 60 sec
Binning: small small small small medium medium
Day: 1 2 3 4 5 6
Peak
Counts
1600
800
1200
400
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14 14
Calibrated Physical Units vs. Raw Signal
Basic Imaging Concepts
Calibrated Signal
(Photons per
second)
Radiance: Photons per
second
Exp time: 30 sec 30 sec 60 sec 60 sec 60 sec 60 sec
Binning: small small small small medium medium
Day: 1 2 3 4 5 6
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15 15
Measurement Table
Measurement table displays information
about each Region of Interest (ROI)
Table is user-configurable and can be
exported to a spreadsheet
Basic Imaging Concepts
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16 16
Reporter Molecules
Biology
Fluorescent dyes
Label Cells Label Bacteria Genetic Marker
+ A
TP
and
O2
– Li
ve c
ells
Quantum dots and
Nanoparticles
+ D
-luci
ferin
sub
stra
te
Fluorescent Proteins
+ excitation light source
Label Proteins
Luciferase
Transfection Direct cell/protein labeling
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17 17
Bioluminescence in IVIS: Unparalleled Sensitivity
Biology
Day 7 Day 14 Day 21 Day 0 Day 28 Day 35 Day 42
104
105
106
107
108
109
1010
1011
0
200
400
600
800
0 6 12 18 24 30 36 42
Photons/sec
Tumor volume
Phot
ons/
sec
Tumor volum
e mm
3
Days post cell implant
Bioware Ultra
Data collection from Day 0
Tumors too small for physical measurement
until 21+ days
5 cells
Visualization 21 days before palpation
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19 19
Dual Reporter: Bacterial luc and GFAP Brain Imaging
Biology
Simultaneous visualization of:
Streptococcus pneumonia (lux)
Glial Fibrillary Acidic Protein -
GFAP (luc)
luc and lux in Pneumococcal Meningitis
Kadurugamuwa et al., Inf. And Immun. 2005
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21 21
Dual Bioluminescence and Fluorescence for Molecular Profiling
Biology For assistance: April Blodgett (508) 589 7461 or [email protected]
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22 22
Ex vivo Analysis for Validation
Biology
Transgene upregulation in brain
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23 23
Attenuation of Bioluminescent Probes
Experimental Design
Optimal Imaging Window
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24 24
Plateau > 95% Max 10-20 min
Luciferin Kinetics Critical for Quantitative Reliability and Reproducibility
Diffuse Light Imaging Tomography
0%
10%
20%
30%
40%
50%
60%
70%
80%
90%
100%
110%
0 10 20 30 40 50
Substrate Distribution Highly Variable
Substrate Clearance Highly Variable
Perc
enta
ge M
axim
um In
tens
ity
Immediate availability
Uniform Distribution
Optimal Imaging Window
Time (min) Post Substrate Injection
Intraperitoneal (i.p.) Injection
Immediate availability
Need to wait for uniform substrate distribution
Optimal imaging window where > 95% of max signal intensity observed
Plateaus typically 10-20 minutes in duration
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25 25
Challenges of Fluorescence Imaging – Diffusion, Scattering AND Autofluorescence
Excitation light needed for
fluorescent sources
Light traveling through tissue
scatters many times creating a
"fuzzy" image at the surface
of the animal
The IVIS® views the diffuse
image on the surface of the
subject
With fluorescent sources, the
diffusion pattern is overlaid
with autofluorescent signal
from skin
Experimental Design
CCD
Optics
Fluorescent
Source
Epi-fluorescence
Light Source
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26 26
Attenuation of Fluorescent Probes
Experimental Design
Optimal Imaging Window
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27 27
Fluorophore Spectra and Autofluorescence
Experimental Design
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28 28
Animal Diet Autofluorescence
Experimental Design
Alfalfa detection highest between
660 and 740
Many 645 and 680 nm probes
overlap
Low autofluorescence chow
helpful if working in this range
Research Diets
http://www.researchdiets.com
AIN-76A (D10001i) – alfalfa free
750 probes allow one to bypass
these issues as well
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29 29
Depilation – Important Regardless of Modality
Experimental Design
Abdominal
Fur removal via depilation increases intensity for BOTH bioluminescent and fluorescent models
All fur attenuates
Dark fur most attenuating
Shaving prior to depilation is
preferred
Caustic - Do not leave on
mouse skin for extended
periods!
Repeat periodically when new
hair growth is visible
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30 30
Positioning – Important Regardless of Modality
Experimental Design
Determine optimal
positioining
Keep positioning
consistent for most
accurate quantitative
data
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31 31
Sensitivity is a Function of a Signal to Noise
Advanced Fluorescence Imaging
Luminescent Sources:
Signal brightness generally lower than
fluorescent sources
Higher sensitivity due to low level noise: both
instrument and animal autoluminescence
Fluorescence Sources:
Signals generally brighter than luminescent
sources
Lower sensitivity due to higher noise: instrument
background and autofluorescence
Instrument
Background
Autofluorescence
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32 32
Improvements to Signal to Noise Ratio
Advanced Fluorescence Imaging
Adaptive FL Background Subtraction:
Software tool to reduce instrument
background
Spectral Unmixing:
Extracts fluorescent signal from
autofluorescence
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33 33
IVIS® Spectrum CT Fluorescence Components
Advanced Fluorescence Imaging
0
20
40
60
80
100
400 440 480 520 560 600 640 680 720 760Wavelength (nm)
Tran
smis
sion
%
10 excitation filters Emission
filter wheel
Excitation
filter wheel
Lens
assembly
Optical
switch
Transillumination
Fiber bundle
Heated
sample
stage
CCD, TE-
cooled to -
90C
18 emission filters
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34 34
Fluorescence Acquisition
Advanced Fluorescence Imaging
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35 35
Fluorescent Calibrated Units: Radiant Efficiency
Advanced Fluorescence Imaging
Compensates for non-uniform excitation light pattern
vs.
Co
un
ts
Rad
ian
t E
ffic
ien
cy
Radiant Efficiency =
Emission Light (photons/sec/cm2/str)
Excitation Light (mW/cm2)
_________________________
Excitation Light Pattern
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36 36
Spectral Unmixing Introduction
Advanced Fluorescence Imaging
What is Spectral Unmixing?
Simply put – separating colors
Pixel by pixel analysis that allows for distinguishing components in an image based on wavelength
Why use Spectral Unmixing?
Increase signal to noise when high levels of autofluorescence are present
Specifically separate co-localized probes
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37 37
Spectral Unmixing Introduction
Advanced Fluorescence Imaging
XLC680
QD705
QD805
XLC750
How is Spectral Unmixing accomplished? Images acquired at multiple wavelengths Pixels mapped and grouped based on peak Pick emission filters centered around component peaks
680nm 840nm
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38 38 Advanced Fluorescence Imaging
0
0.2
0.4
0.6
0.8
1
1.2
400 450 500 550 600 650
No
rma
lize
d I
nte
nsit
y
Wavelength (nm)
AutofluorescenceExcitation
tdTomato Excitation
535nm
Excitation
Filter
580nm Emission Filter
Spectral Unmixing – Removing Autofluorescence
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39 39
Tissue AF
tdTomato
540 620 640 660 680 560 580 600
Wavelength (nm)
.5
1.0
Normalized
Amplitude
S:N = 1.5 S:N = 4053
580 600 620 640 660
540 560 580 600 620 640
680
Spectral Unmixing – Removing Autofluorescence
Advanced Fluorescence Imaging
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40 40
Spectral Unmixing - Modes
Advanced Fluorescence Imaging
Automatic
Traditional Caliper method
Fully automated
Fluorophore spectral libraries pre
loaded
Easiest but least exact
Compute Pure Spectra
Traditional CRi method
Manual control by user
Spectral libraries created by user
Uses a type of image math to
subtract autofluorescence from
“mixed components”
Three modes: Manual
Guided
Library
More input required but typically better
outcome – higher S:N
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41 41
Spectral Unmixing - Library Generation
Autofluorescence
Control
ProSense 680
Control
Integrisense 645
Control
Tumor
No Dye
No Tumor
Both Dyes
Tumor
1 Dye
Tumor
1 Dye
Tumor
Both Dyes
Advanced Fluorescence Imaging
• Effective spectral unmixing requires good library
• Library gives the software the spectral
information for individual components of the
image
• User generated thereby tailored for your
experiment
• Effective library generation begins with inclusion
of proper controls
• Autofluorescence control critical, use either: • Naïve animal handled same way
• Diseased with no probe injected
• Nonspecific control elucidates sites of probe
clearance
• For experiments involving simultaneous injection
of more than one probe, have one control for
each probe to be used
Controls
Nonspecific
Control
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42 42
Spectral Unmixing – Library Generation
Advanced Fluorescence Imaging
• Manual Unmixing
• Mark pixels to
generate average
curve
• Label appropriately
• CPS – Image Math
to subtract
autofluorescence
component and
generate Pure
components
• Unmix
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45 45
R² = 0.7095
0.00E+00
2.00E+08
4.00E+08
6.00E+08
8.00E+08
1.00E+09
1.20E+09
1.40E+09
1.60E+09
1.80E+09
0.00E+00 1.00E-07 2.00E-07 3.00E-07 4.00E-07 5.00E-07 6.00E-07
Tota
l Sig
nal
Concentration (mg)
Monochrome: Total Signal vs. Concentration
R² = 0.9117
0.00E+00
1.00E+08
2.00E+08
3.00E+08
4.00E+08
5.00E+08
6.00E+08
0.00E+00 2.00E-07 4.00E-07 6.00E-07
Tota
l Sig
nal
Concentration (mg)
Unmixed: Total Signal vs. Concentration
Advanced Fluorescence Imaging
Why Perform Spectral Unmixing? Quantitation
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46 46 Advanced Fluorescence Imaging
Shcherbakova, DM and Verkhusha VV., Nat. Met. 2013
In vitro
Ex vivo • Unmixing prevents crosstalk between far and
near infrared reporters
• Allows visualization of colocalization and accurate
quantitation in vivo, in vitro or ex vivo
Why Perform Spectral Unmixing? Multiplexing
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51 51
IVIS Spectrum CT Transillumination
Advanced Fluorescence Imaging
Selected excitation positions denoted by
crosshairs in acquired image
Subject Stage
Excitation Light Source
Select desired locations in
Living Image
for Raster scan
Optimized for imaging deep signals,
improves Signal:Noise ratio
Avoids problems from whole body
autofluorescence created from Epi-
illumination
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52 52
Normalized Transmission Fluorescence
Advanced Fluorescence Imaging
Fluorescence Filter pair specific for probe
Standard wizard setup
Transmission Neutral density filter
White light
Tissue optical density
No user input required
Automatic when Normalized
checked – default for 2D
transillumination
535nm Ex
620nm Em
ND2
620nm Em
÷ =
NTF Efficiency is unit of measure
for 2D transillumination
Negative exponent – large
denominator
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53 53
Epi vs. Transillumination Imaging of XL680, XL750 and QD800
Advanced Fluorescence Imaging
CF680 dye
25 picomole
CF680 dye
250 picomole
CF750 dye
250 picomole
QD800 dye
4 picomole
EPI NTF EPI NTF
S/B: 0.81 S/B: 6.69 S/B: 1.18 S/B: 2.47
S/B: 1.11 S/B: 9.19 S/B: 1.11 S/B: 4.27
S/B: 1.31 S/B: 8.32 S/B: 1.05 S/B: 2.57
CF750 dye
25 picomole
QD800 dye
0.4 picomole Detect 0.4 picomole
Qdots in the lungs
Transillumination optimal for deep tissue imaging – greater sensitivity at depth
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54 54
Benefits of 3D Imaging – Why I Need It?
Algorithms account for
diffusion, scattering
and attenuation
pmol
Over 6000 publications using
FLI and BLI in vivo, ex vivo,
and in vitro in numerous
models
HOWEVER, transillumination facilitates detection of
probes in deep tissue
2D
3D
Calibrated to NIST standard – 2D quantitation is
cornerstone of most IVIS publications!
Calibration curves
translate radiance units
into pmol or cells
Tran
s Ep
i
Anatomical context allows
for pinpoint localization
Ability to answer more
complex biological
questions
Localization from 2D
imaging difficult without
ex vivo confirmation
Due to diffusion, 2D surface
radiance is less exact when
determining localization of probes
3D reconstruction can elucidate
location of multiple probes in
relation to each other
Flexible, fast, easy!!!
Thompson SM et al. (2013). Invest Radiol 48:413–21.
Shcherbakova, DM.. Nat. Met. 2013
Zhang et al, Nature Medicine (2013)
Li,
Ch
un
shen
g, e
tal.
On
cota
rget
201
4
Collins JW et al. (2012) Microbiology 158:2826–34.
Lee J et al. (2011). BMC Neurosci 12:9
Cronin M, et al. (2012) PLoS ONE 7(1): e30940.
Cronin M, et al. (2012) PLoS ONE 7(1): e30940.
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55 55 3D Optical Tomography
Quantification – Attenuation Correction
“2D BLI imaging …80% reduction in average radiance
and 71.8% reduction in total flux“
“3D DLIT ….20.2% reduction in total flux, a 16.7%
decrease in source volume, and a 1.5 mm increase in
source depth (8.3 to 9.8 mm”
“Gross pathology confirmed a medial necrotic zone
….lateral area of grossly viable tissue”
“Microscopic pathology confirmed that approximately
14.9% of the total tumor area demonstrated morphologic
evidence of coagulative necrosis.”
Changing depth impacts surface radiance
more intensely
Algorithms account for red shifting due to
attenuation
Resultant values at times more indicative
of actual in vivo outcome 1.00E+04
1.00E+05
1.00E+06
1.00E+07
1.00E+08
1.00E+09
540 560 580 600 620 640 660
Shallow
Deep
Early timepoints:
Viable cells shallower
Later timepoints: Necrosis
Viable cells deeper
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56 56
Quantification
Transillumination provides consistent quantitative analysis
throughout the range of dilutions
Epi-illumination values consistently 2-3 fold lower than
expected
3D results show accurate location and volumetric
approximation even with decreasing intensity
Experimental Design
GastroSense 750 serially diluted and orally gavaged into nude
mice
Epi vs Transillumination/FLIT performed for detection and
quantification.
Source Perkin Elmer Technical Note - Optical Imaging on the IVIS Spectrum CT System: General and Technical Considerations for 2D and 3D Imaging
3D Optical Tomography
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57 57
Quantification – Transillumination Facilitates Deep Tissue Detection and 3D
Reporter 3D ROI Total Cells
Firefly Luc ROI 1 4.07E+07
3D ROI Total pmol
IntegriSense 750 ROI 1 2.34E+03
Experimental Design
1 million 4T1-rLuc injected directly into lungs 2
weeks prior
Integrisense 750 injected 24hrs prior to imaging
Bioluminescence signal
expressed in # cells
Healthy
Diseased
Fluorescence signal
expressed in pmol
3D Overlay
BLI, FLI,
Colocalized
Heavy tumor burden in lungs around 40 million viable cells
causing decrease in air volume visible via mCT
Around 2 nmol Integrisense 750 detected in lung cavity
specifically in areas of heavy tumor burden as indicated by
colocalized signal
αvβ3 integrin upregulation in tumor cells indicating growth,
viability, and angiogenesis
cells pmol
Epi-illumination not capable of distinguishing IntegriSense
750 from background in lungs
Transillumination facilitates both detection and 3D analysis
2D 3D
BLI Epi Trans
Unpublished results – PerkinElmer 3D Optical Tomography
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58 58
Colocalization
“confirm the specific localization of 78Fc to hTEM1-positive
grafts”
“bioluminescent and NIR fluorescence signals overlapped only
at the site of hTEM1-positive grafts”
“fluorescence was observed in the livers of these mice”
“demonstrated that 78Fc750 was specifically enriched in
hTEM1-positive tissues.”
“observed a localized tumor mass in the cortex”
“GFAP activity was upregulated more broadly in the areas
surrounding the tumor….In agreement with the
immunohistochemical data”
“suggesting that the GFAP response in the luciferase
reporter extends beyond the immediate tumor margin”
2D surface radiance is impacted by
scattering and diffusion.
Determinations about colocalization at
depth purely based on 2D is risky
especially in deeper tissue.
3D colocalization can aide in confirming
colocalization at depth.
3D Optical Tomography
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59 59
Coregistration – Pinpoint Localization/Anatomical Context
Day 13 Day 20
UPEC inoculated into the bladder and ascend the
ureter to cause pyelonephritis
3D identified localization in intestinal tract after
ingestion
Anatomical context to optical reconstruction
Pinpoint localization
3D Optical Tomography
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60 60
Coregistration – Pinpoint Localization
“GAP-43 signals were indeed arising from
the areas surrounding the brain
structures normally affected by MCAO,
including parts of the frontal and parietal
cortex, striatum, and hippocampus.”
“These findings were further validated by
immunohistochemistry analysis.”
2D surface radiance is impacted by scattering/diffusion/attenuation.
Exact determinations about location purely based on 2D is impossible in vivo in deeper
tissue areas.
Unpublished data courtesy Dr. Adrienne Scheck, Barrow Neurological Institute,
Phoenix, AZ
3D provides depth
and MRI
coregistration
confirms pinpoint
localization of tumor
in brain
2D provides no
specific information
about brain region
“The measured tumor depths
ranged from 1.2 mm to 6.8
mm”
“At the sites of tumor
metastases, osteolytic
lesions were evident by mCT
imaging”
“co-registered the 3D
bioluminescent images with 3D
mCT images to display all
metastatic lesions in a referenced
anatomical setting.”
3D Optical Tomography
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61 61
Coregistration – Anatomical Context
“facilitated the anatomical
positioning of bioluminescent signal
sources within the tumour”
“in addition to visualisation of
tumour vasculature through
administration of a contrast agent.”
“Peak luminescence levels within the
large intestine region, correlating with
results obtained by sampling and culturing”
“The proximity …to the pancreas prevented the accurate
delineation of a ROI encompassing solely the pancreas on PET
images.”
“An ROI comprising only the pancreas (red dashed line in Fig. 1 D
and E) was defined by using the tomographic bioluminescence
image”
“allowed for unambiguous delineation of the pancreas ROI in …
PET image … enabled us to quantify the pancreatic PET signal while
minimizing the confounding influence …. signal from adjacent
organs.
“UCC2003 was detected solely in
necrotic regions, as evidenced by
PCR. 3D…imaging provides in vivo
evidence of this here”
3D Optical Tomography
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62 62 3D Optical Tomography
Single View 3D Imaging is a Two-Step Process
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63 63
Surface Topography Reconstruction – Step 1
3D Tomography
CT scan needed
Full body CT scan
Fast or Standard Resolution option
Use threshold presets to determine
edges of subject
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64 64
DLIT - Spectral Measurements Provide Information on Depth of Source
Bioluminescence Tomography
In vitro ROI data, 20 nm bandpass filters
In vivo
Subcutaneous
In vivo
Chest Cavity
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67 67
Luciferin Kinetics Critical for DLIT
Bioluminescence Tomography
Subcutaneous
Brain
6 Minute
Intervals
Burgos et al., 2003
Remember! Consistent light output assumed for algorithmic
reconstruction
Roughly 8
minute
window
All 5 images need to be
acquired in this timeframe
Careful of factors that may affect
curves – localization, handling,
metabolism
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68 68
DLIT Reconstruction
Bioluminescence Tomography
Select tissue properties
• Select wavelengths
Select source spectrum
Threshold your data
Chest Cavity Peritoneal Cavity
Depth
[mm]
Flux
[photons/sec]
Depth
[mm]
Flux
[photons/sec]
2.1 2.43108 3.2 1.44108
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69 69
Automatic Mouse Atlas Registration
3D Tomography
Anatomical localization in Spectrum
Optical
Optical- CT
Optical- CT- Organ Atlas
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71 71
Transillumination Facilitates 3D Reconstructions of Fluorescent Sources
Fluorescence Tomography
Kidneys
Kidneys
Subject Stage
Excitation Light Source
Selected
excitation
positions
denoted by
crosshairs in
acquired
image
Select desired locations in Living Image
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72 72
Transillumination Excitation at Multiple Points for Source Localization
Fluorescence Tomography
D1 D3 D10 D5 D7 D12
S1 S2 S3 S4 SN
Mouse
Detector
Excitation
source
Tumor
DN D16
The excitation source scans the subject
The CCD collects multiple projections using designated emission filter
Tumor
Angle and intensity of projections
facilitates reconstruction of
source localization and intensity
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73 73
FLIT Reconstruction
Fluorescence Tomography
Select tissue properties
• Select images
Threshold your data
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74 74
Reagents and Instrumentation - 3D Tomographic Analysis
3D Tomography For assistance: April Blodgett (508) 589 7461 or [email protected]
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75 75
HTC116 Cancer Signal Brevibacterium Bacterial Signal Dual Cancer/Bacterial Signal
Mark Tangney and Cormac Gahan, University of Cork
Bacterial Targeting of Tumors – Dual Reporter 3D Tomography
3D Tomography Cronin et al., PLOS One, 2012
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76 76 3D Optical Tomography
Liver Toxicity – Deep Tissue Fluorescence Imaging/Anatomical Context
Injectable probes offer valuable insights into the molecular
mechanisms involved in disease progression – necrosis,
angiogenesis, apoptosis, hypoxia, tissue viability
2D epillumination analysis allows visualization of necrosis in the
liver and bladder compared to control
However, 3D tomography facilitated by deep tissue detection
capabilities of transillumination elucidates deeper AnnexinVivo
signals and facilitates compartmentalization of signals
Anatomical context provides information about pinpoint location of
probes and tomography allows quantitative analysis of probe
concentrations in deeper tissues
In contrast to 2D, 3D allows simultaneous monitoring of necrosis
and clearance of the probe through the kidneys
Kidneys
2D
Control 48 hrs. post thioacetamide administration
Total Signal
Liver
Kidneys
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78 78
Use Well Plate Quantification Library to Determine pMol or Cell Number
3D Tomography
Dilute your cells or dye and image
Select Well Plate Quantification from Tools menu
Enter cell number or
concentration per well
Save as a library
Choose library when
reconstructing
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80 80
Absolute Quantification and Anatomical Reference
3D Tomography
Healthy
Diseased
Healthy Diseased
Sequence Number 3D ROI Voxels Total Cells Average Cells
BRE20130626193512_SEQ ROI 1 10684 4.07E+07 3.81E+03
Sequence Number 3D ROI Voxels Total pmol Average pmol
BRE20130626195138_SEQ ROI 1 14025 2.34E+03 1.67E-01
1 million 4T1-rLuc injected directly into
lungs 2 weeks prior
Integrisense 750 injected 24hrs prior to
imaging
Diseased lungs show decrease in lung air
volume via µCT
Bioluminescence signal
expressed in # cells
Fluorescence signal
expressed in pmol
3D Overlay
BLI, FLI,
Colocalized
Heavy tumor burden in lungs around 40 million viable cells
causing decrease in air volume
Around 2 nmol Integrisense 750 detected in lung cavity
specifically in areas of heavy tumor burden as indicated by
colocalized signal
αvβ3 integrin upregulation in tumor cells indicating growth,
viability, and angiogenesis
cells pmol
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81 81 Introduction
Micro-Computed Tomography (µCT)
Provides anatomical reference and structural
measurements
Calibrated measurement in Hounsfield units
Utilized to reconstruct surface for DLIT and
FLIT
Can generate 2D X-ray projection onto 2D
bioluminescent or fluorescent images
User friendly setup and analysis
2D X-ray overlay
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82 82 Mechanics
How µCT Works
How µCT Works
Higher energy
Voltage = 50 kV
Current = 1 mA
Higher tissue density = Higher attenuation
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83 83
Attenuation = 1/Penetration
Increasing photon energy generally
decreases attenuation
Higher energy photons are more penetrating
Calibrated automatically for Hounsfield unit
scale.
Linear transformation of the original linear
attenuation coefficient measurement
Radiodensity of distilled water at STP is 0
Radiodensity of air at STP is -1000
Density of tissue dictates HU
Theory
mCT Analysis and Units
Penetration
mx – mwater
mwater HU = 1000 x
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84 84 Mechanics
Scan Options with µCT
Mode Name Resolution (mm) Voxel Size (mm) FOV
L x W x H (cm) Binning Dose (mGy) Scan Time Typical Use
Fast 850 300 12.5 x 12.5 x 3 4 13 3.6
Needed for
FLIT/DLIT,
longitudinal CT
Standard
(1 Mouse) 425 150 12.5 x 12.5 x 3 4 53 14.4 Anatomical
reference, largest
FOV Standard
(2 Mice) 425 150 12.5 x 12.5 x 3 4 23 36
Medium Res 225 75 6 x 6 x 3 2 132 36 Best for soft tissue,
organ contrast
High Res 150 40 2.4 x 2.4 x 2 1 46 72 Bone detail, implant
study
High Res Top 150 40 2.4 x 2.4 x 2 1 46 72 Bone detail, implant
study
Limitations of X-ray Dosage
Immuno-compromising Dose = 1000-2000 mGy
LD 50/30 Dose = 5000-7500 mGy
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85 85 Computed Tomography
Resolution
Fast 850 mm
Standard 450 mm
Medium
225 mm
High
150 mm Best for
anatomical
reference
Best for use in CT analysis
Optimal for soft
tissue contrast
Highest
resolution
CT only
Turn X-ray on with the
provided key
When armed, the
Acquire button will
display this message
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86 86
mCT Analysis – Multimodality Module Overview
3D ROI for Hounsfield Unit
Render 2D X-ray view for overlay
onto bioluminescent or fluorescent
images
Crop and adjust histogram to
segment based on density
Multimodality - Software
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87 87
Visualization Tools
Data can be cropped to remove unwanted regions or to
slice into animal for visualization purposes
Before cropping Crop on X Crop on Y Crop on Z
Multimodality - Software
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88 88
Visualization Tools
Histogram shows distribution of voxels from least to most dense – lowest to highest HU
Maps can be generated to isolate voxels of a particular density, saved and reused
Used to isolate
tissues and/or
contrast agents
Bone
Bone and Lung
Bone and Exitron/Vasculature
Multimodality - Software
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Visualization Tools
Data can be displayed in two ways: Gradient – Enhances boundaries between homogeneous regions
Maximum Intensity Projection (MIP) – Projects maximum intensity voxels in viewing plane
Multimodality - Software
MIP Gradient
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Visualization Tools
3D animation tools for generating videos
Multiple video formats available for export
Multimodality - Software
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Visualization Tools
Slice tab allows for visualization of multiple slices simultaneously
Raw data mode or Volume Color Table mode if you wish to see segmented components only
Color scale adjustments can be applied to brighten or darken images
Multimodality - Software
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Visualization Tools
Three main groups of tissue
can be imaged with CT: Bone
Fat
Soft tissue
Lungs can typically be
visualized due to the
presence of air within the
organ
Utilizing heat maps may
improve visualization of
tissues when compared
to grey scale
Multimodality - Software
Fat Soft Tissue
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3D Analysis
For proper data analysis, datasets should be normalized to a common scale bar
Utilizing newly included tools, common settings can be applied across a group of images
View of the images, can be synced as well
Software
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Automatic Mouse Atlas Registration
Utilize mouse atlas as further confirmation of organ location when lacking contrast
Software
Optical Optical - CT Optical- CT- Organ Atlas
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For an In-Depth Study
IVIS University Web page
www.perkinelmer.com IVIS Software Manual
IVIS Software Manual
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Learning Resources
Conclusion
In Vitro Bioluminescence, In Vivo Bioluminescence, In Vitro Fluorescence, In Vivo Fluorescence
Click Image or Links Below for Further Information
Jove Video Resources Online Training Videos
Optical and Micro-computed Tomography (CT) on the IVIS Platform
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Top Ten Tips for Optical Imaging
1. Choose reporters that maximize signal-to-noise (S:N) ratio
2. Consider the appropriate control groups and imaging time points necessary
3. Use hairless mice or white-furred animals and depilate or shave
4. Switch to autofluorescence-free mouse diet
5. Closely map the kinetics of your biological bioluminescent model
6. Animal handling can significantly affect kinetics
7. Image in the animal orientation that yields the highest signal intensity
8. Cover intense signal to allow dimmer signals to dictate auto-exposure
9. Utilize guards to prevent reflection off neighboring animals
10. Use black well plates when doing in vitro experimentation
http://www.genengnews.com/experttips/10-tips-for-successful-in-vivo-optical-imaging/4573
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Thank you for your attention!
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