A Multimodal Imaging Approach Based on Micro-CT and Fluorescence Molecular Tomography for Longitudinal Assessment of Bleomycin-Induced Lung Fibrosis in Mice

Podsumowanie

We describe a non-invasive multimodal imaging approach based on Micro-CT and fluorescence molecular tomography for longitudinal assessment of the mouse lung fibrosis model induced by double intratracheal instillation of bleomycin.

Streszczenie

Idiopathic pulmonary fibrosis (IPF) is a fatal lung disease characterized by the progressive and irreversible destruction of lung architecture, which causes significant deterioration in lung function and subsequent death from respiratory failure.

The pathogenesis of IPF in experimental animal models has been induced by bleomycin administration. In this study, we investigate an IPF-like mouse model induced by a double intratracheal bleomycin instillation. Standard histological assessments used for studying lung fibrosis are invasive terminal procedures. The goal of this work is to monitor lung fibrosis through noninvasive imaging techniques such as Fluorescent Molecular Tomography (FMT) and Micro-CT. These two technologies validated with histology findings could represent a revolutionary functional approach for real time non-invasive monitoring of IPF disease severity and progression. The fusion of different approaches represents a step further for understanding the IPF disease, where the molecular events occurring in a pathological condition can be observed with FMT and the subsequent anatomical changes can be monitored by Micro-CT.

Wprowadzenie

Idiopathic pulmonary fibrosis (IPF) is chronic lung disease with progressive decrease of lung functions that is unfortunately often fatal within four years of diagnosis¹. The major features of IPF are extracellular matrix deposition and fibroblast proliferation, but the pathogenesis is not yet fully understood. The most supported hypothesis is that multiple cycles of lung injuries cause the destruction of alveolar epithelial cells that leads to alteration of the mesenchymal cell cycle proliferation, exaggerated accumulation of fibroblasts and myofibroblasts, and increased matrix production. Mediators involved in these processes such as matrix metalloproteinases (MMPs) have been found dysregulated in fibrosis development either in human IPF or in bleomycin-induced animal models. The uncontrolled MMP production leads to an unbalanced collagen deposition within the lung interstitium and alveolar space, mimicking abnormal wound repair^1,2.

One of the main obstacles for drug discovery and development is the availability of accessible mouse models that mimic human pathogenesis and the disease phenotype. Different agents have been used to induce lung fibrosis in animal models: irradiation damage, administration of asbestos and silica, administration of fibrinogenic cytokines and bleomycin^3,4; however bleomycin is the most used in mice, rats, guinea pigs, hamsters, rabbits⁵ or in large animals (non-human primates, horses, dogs and ruminants)^6,7. Bleomycin is an antibiotic made by the bacterium Streptomyces verticillus⁸ and is used as an anti-cancer agent⁹. Pulmonary fibrosis is a common side effect of the drug and for this reason, it is used in experimental animal models to induce pulmonary fibrosis.

In bleomycin-induced lung fibrosis models, the fibrotic lesions occur 14 - 21 days after bleomycin administration. In the presented work, we used a new protocol to induce lung fibrosis in mice by double bleomycin intratracheal instillation. The bleomycin mouse model is very time consuming because new drugs need to be evaluated on established fibrotic lesions, and tested to distinguish their anti-fibrotic effects from anti-inflammatory effects.

Biochemical determination of collagen content, morphometrical and histological analysis were based on post mortem analysis, limiting the possibility to follow the pathogenesis of the disease in the same animal. Although these parameters were considered a gold standard for fibrosis evaluation, they did not provide any temporal or spatial distribution of the fibrotic lesion and preclude a way to investigate the process of disease progression.¹⁰

Recently, non-invasive imaging technologies have been applied to monitor airway remodeling, inflammation, and fibrosis progression in murine models: Magnetic Resonance Imaging (MRI), Micro Computer Tomography (Micro-CT), Fluorescence Molecular Tomography (FMT) and Bioluminescent (BLI)^{11,12,13,14,15,16,17,18,19,20,21}. We propose a non-invasive imaging approach to monitor longitudinally lung fibrosis progression by FMT and Micro-CT at different time-points after a bleomycin challenge²².

Many pathways are involved in the establishment and development of fibrosis, and not much is known. Only a deeper understanding of these processes could translate to more drug targets that may transfer into the clinic. The ability to longitudinally monitor MMP activation by fluorescence molecular tomography coupled to the detection of lung parenchymal changes by Micro-CT might be used in the future to access the clinical response to treatment.

Protokół

All animal experiments described herein were approved by the intramural animal-welfare committee for animal experimentation of Chiesi Farmaceutici and ERASMUS MC under protocol number: EMC 3349 (138-14-07) complying with the European Directive 2010/63 UE, Italian D.Lgs 26/2014 and the revised "Guide for the Care and Use of Laboratory Animals"²³.

NOTE: Prior to use, female inbred C57Bl/6 (7-8 weeks old) mice were acclimatized for at least 7 days to the local vivarium conditions (room temperature: 20-24 °C; relative humidity: 40-70%; 12-h light-dark cycle), having free access to standard rodent chow and softened tap water.

1. Intratracheal Treatment of Mice with Bleomycin

1. Prepare the equipment for the intra-tracheal instillation^12,13,14.
2. Put the mice in the anesthetic chamber connected to an isoflurane vaporizer set at 2.5% mixed with oxygen. Check for depth of anesthesia by the lack of a toe-pinch response. The effect of the anesthesia occurred after 3-5 min.
3. Position the anesthetized mouse on the intubation platform, hanging it by its incisors placed on the wire.
4. Turn on the laryngoscope, take a pair of blunt ended forceps and use either the forceps or laryngoscope's tip to gently open the mouth.
5. Pull out the tongue and hold it to the side with forceps. Place the laryngoscope blade towards the back of the mouth until the opening of the trachea is visualized and keep the laryngoscope in place.
6. With the other hand, insert the delivery tube connected to the end of the PE tubing into the trachea, rotating the three-way valve. Deliver 50 µL of bleomycin (0.020 µg/mouse). After instillation, quickly remove the tube from the trachea to prevent suffocation. Hold the mice upright for a few seconds.
   1. Administer bleomycin intratracheally at day 0 and repeat at day 4 (Figure 1).
7. Remove the mouse from the intubation platform and monitor the mouse for 30 min (the time needed to fully recover from anesthesia).
8. Perform in vivo imaging of the mice lungs by FMT and Micro-CT after double bleomycin instillation at day 7, 14, and 21.

2. In vivo Imaging by Fluorescence Molecular Tomography

NOTE: Beforehand, prepare a fresh stock solution of 6 nmol/mL of MMP sensitive fluorescent substrate 680 in saline solution (0.9% sodium chloride), and store protected from the light at 4 °C before use. It is stable for up to 6 months at 4 °C. Allow MMP imaging agent to equilibrate to room temperature before injecting into animals.

1. Probe injection
   1. Prepare the equipment for intravenous injection of the MMP probe solution. Pre-warm water at 50 °C to heat the mouse tail.
   2. To firmly grasp the mouse scruff, take it by the tail and allow it to grip the cage lid. Holding the mice across the animal's shoulders, put the tail in a warm water beaker, for 4 to maximum 8 s thermal injury to prevent thermal injury to the tail skin.  Check the veins swelling for easier visualization and needle insertion.
   3. During the injection procedure, put the mice into a plastic restrainer to keep it steady and pull the tail through a special hole in the back. Find the two caudal veins on either side of the tail; not the artery on the underside of the tail.
   4. Insert the needle (26G) of the 1 mL syringe into the vein. If the needle is correctly placed, injection will be easy and the probe solution will flow into the vessel.
   5. Inject the MMP probe solution at 10 mL/kg.
   6. Discard the needle.
      NOTE: The optimal imaging time point is 24 h after the MMP probe injection because it is the time required by the probe to be activated. If longitudinal studies are performed, the optimal re-injection time is 7 days, which allows for the complete clearance of the agent from the mouse.
2. FMT imaging
   NOTE: Before starting, always remove the fur on and around the areas of the animal that are to be imaged, in this case the chest, to avoid scattering and absorbance in tissue.
   1. To anesthetize the mouse, put it in anesthetic chamber and turn the isoflurane dial to 2.5% for induction and 2% for maintenance.
   2. Initialize the data acquisition software and open a new study in the database for the experiment.
   3. Before starting the imaging with FMT, transfer the mouse into the imaging cassette. Place the anesthetized mouse in the middle of imaging cassette to optimally use the field of view of the FMT. Keep the mice flat, secure and gently compressed against both windows of the imaging cassette. Adjust the height by knobs on the cassette, and then slide it into the docking station.
   4. Click on subject in the scanning window and click preview to see the live image.
   5. Draw the scan region sufficiently large so that tissue surrounding the anticipated area of fluorescence is captured. Including a total of 25 scan points guarantees the lung region will be totally scanned.
   6. Once the ROI is drawn, first click add to reconstruction queue and then click Scan to image the mouse. Make sure that the correct laser at 680 nm is selected.
   7. When the image acquisition is completed, place the mouse back into its cage. Be sure it fully recovers from anesthesia.
   8. Quantify the picomoles of fluorescence in the Analysis window of the analysis software using the ROI tool and reduce the ROI around 700-800 mm³ on the signal coming from the lung region. Be careful to exclude the liver signal. Copy the ROI on the other subjects to have them similar in dimension and adjust their position in each animal image.
   9. Export images as jpg files.

3. In Vivo Imaging by Micro-CT

CAUTION: Before starting, always remove any metal jewelry or metal objects near the imaging area, to avoid scattering of x-rays.

NOTE: Radiation-induced lung fibrosis is a common finding during radiation induced lung injury²⁴. Neither Micro-CT derived indices nor histological findings associated with lung fibrosis were present in saline treated control mice on day 21 subjected to four Micro-CT imaging sessions, indicating that the X-ray dose delivered to the animals during Micro-CT examinations was not sufficient to affect the findings.

1. Turn on the Micro-CT by pressing the green power button and launch the software to warm up the x-ray source. Use the small bore and the animal bed for mice imaging.
2. Create the database by clicking on New database for a new one and build the browser based on number of mice in the experiment, or click connecting to existing database to save the data to a previously created one.
3. Before starting the scanning, select the acquisition parameters in the software control window: X-ray tube voltage, 90 kV; CT X-ray tube current, 160 µA; Live X-ray tube current, 80 µA; FOV, 36 mm; No gating technique; Scan technique, High resolution 4 min.
4. Anesthetize the mice by inhalation of 3% isoflurane and place them on the bed inserted into the bore with a nose cone providing a constant supply of anesthetic. Immobilize the paws of the mice with tape on the bed to allow the chest to be exposed.
5. Slide the instrument door and turn on the Live Mode to see the mouse position in real time by pressing the capture button. Move the animal bed to align the chest with the field of view (FOV) using buttons directly located on the CT instrument. Center the scan on the mouse; if not adjust the position with left and right arrows located on the CT instrument.
6. Confirm optimal bed position by rotating the gantry by selecting 90° and clicking Set. Make sure that the region to image is fully inside the FOV.
7. Do not apply any gating technique and start the scan by clicking the CT Scan button. Click yes to the message that informs that the x-ray source will be turned on.
   NOTE: Once the x-rays are turned on, the orange lamp on top of the instrument will be illuminated and the sliding door will be impossible to open for the safety of the operator. Once the scan is finished, a new window of the 2D Viewer software appears showing the transaxial, coronal, and sagittal slice of the reconstruction.
8. Check the image quality and be sure not to have blurred images from movements due to the low level of anesthesia. If necessary, repeat the scan.
9. Place the animals back into the cage and be sure they fully recover from anesthesia.

4. Bronchoalveolar Lavage

1. Anesthetize animals with 3% isoflurane and sacrifice by bleeding from the abdominal aorta.
2. Use scissors to expose the thoracic cage and neck. Then expose the trachea and make a small incision to allow the BAL procedure to be performed with a 21-gauge lavage tube attached to a 1 mL syringe without the needle. Pay attention not to cut through the trachea.
3. To perform the BAL, fill the 1 mL syringe without a needle with 0.6 mL of sterile solution [10x Hank's balanced salt solution (HBSS); 100 mM ethylenediaminetetraacetic acid (EDTA); 1 mM 4-(2-hydroxy-ethyl)-1-piperazineethansulphonic acid (HEPES); distilled water].
4. Insert the lavage tube into the incision in the trachea and slowly inject and withdraw the solution 3 times, pausing on the third withdrawal to allow optimum collection of the BALF for subsequent analysis.

5. Histology and Histomorphometry

1. Expose and remove lungs, inflating them with a cannula through the trachea by gentle infusion with 0.6 mL of 10% neutral-buffered formalin and store the samples at room temperature for 24 h.
2. Dehydrate samples through different passages in increasing concentrations of alcohol solutions (60% ethanol for 1 h, 70% ethanol for 1 h, 90% ethanol for 1 h, 95% ethanol for 2 h, and 100% ethanol for 2 h) using an automatic tissue processor.
3. Place specimens in xylene for 2 h to make them translucent. At the end of dehydration, infiltrate samples in paraffin at 60 °C for 3 h and embed them in the automated processor.
4. Obtain 5 µm thick serial sections using a rotary microtome.
5. Deparaffinize and rehydrate slides in descending grades of ethanol and stain with Masson's Trichrome using an automatic tissue processor.
6. Manually focus on lung slices, scanning at 20X magnification using a slide scanner and capture digital images of entire lung sections using the viewing software with a resolution of 451 nm/pixel.
7. Morphologically assess fibrotic lung injury by semi-quantitative and quantitative parameters as follows:
   1. Determine the Ashcroft score. Semi-quantitatively grade morphological changes in lung sections according to the scale defined by Ashcroft¹⁰ modified by Hübner et al.²⁵ Use the system of 0-8 score to assess all the parenchyma in the lung sections.
   2. Determine the Collagen content. Quantify the degree of fibrosis^10,25 by the microscope image analysis software. Randomly select three ROIs at 10X magnification, per each slide. By standardization of color threshold settings, detect the collagen as green-stained area.
   3. Determine the Alveolar Air Area. Quantify the alveolar air area as an indirect parameter of fibrosis^10,25. By means of the same software and ROIs applied for the fibrosis fraction, detect the air area within the ROIs using a white threshold.

Wyniki

Spontaneous resolution of the lung fibrosis lesions observed three weeks after single bleomycin administration and moderate structural changes highlight the limits of this model. Only preventive treatment could be performed due to the narrow therapeutic window that does not represent clinical practice¹⁷.

Here, we demonstrate that our protocol of double bleomycin intratracheal instillation is able to devel...

Dyskusje

Despite many research groups focusing on developing new drugs to treat IPF, at the moment only two are available for patients. There is an urgent medical need to find more effective therapies⁷ because only lung transplantationis able to prolong survival of 4-5 years²⁶. The essential prerequisite for translational medicine and development of new drugs is the availability of an animal model that mimics the features of IPF and in which interventional studies are predictive of ...

Materiały

Name	Company	Catalog Number	Comments
FMT 2500 Fluorescence Tomography System	Perkin Elmer Inc.	Experimental Builder
MMPsense 680	Perkin Elmer Inc.	NEV10126	Protect from light, store the probe at 4 °C
TrueQuant software	Perkin Elmer Inc.
Female inbred C57BL/6	San Pietro NatisoneHorst, The Netherlands (UD),		Prior to use, animals were acclimatized for at least 5 days to the local vivarium conditions
Isoflurane	ESTEVE spa	571329.8	Do not inhale
Automated cell counter	Dasit XT 1800J	Experimental Builder
Saline Solution, 0.9% Sodium Chloride (NaCl)	Eurospital	15A2807
Quantum FX Micro-CT scanner	Perkin Elmer Inc.
Bleomycin sulphate from Streptomyces Verticillus	Sigma	B2434
Automatic tissue Processor	ATP700 Histo-Line Laboratories	ATP700
Embedding system	EG 1160 Leica Biosystems	EG 1160
Rotary microtome	Slee Cut 6062
Digital slide scanner	NanoZoomer S60, Hamamatsu Photonics
NIS-AR image analysis software	Nikon
Masson’s Trichrome Staining	Histo-Line Laboratories
10% neutral-buffered formalin	Sigma	HT5012-1CS
Penn-century model DP-4M Dry power insufflator	Penn-century	DPM-EXT
PE190 micro medical tubing	2biological instruments snc	BB31695-PE/8
Syringe without needle 5 mL	Terumo	SS*05SE1	Cut the boards of the piston by scissors
Hamilton 0.10 mL (model 1710)	Gastight	81022
Discofix 3-way Stopcock	Braun	4095111
Syringe with needle 1 mL	Pic solution	3,071,260,300,320	Use without needle
Plastic feeding tubes 18 ga x 50 mm	2biological instruments snc	FTP-18-50	Cut obliquely the tip