Induction of Mouse Lung Injury by Endotracheal Injection of Bleomycin

Podsumowanie

Here we present an effective method to investigate the antifibrotic activity of intravenously infused human mesenchymal stromal cells obtained from the whole umbilical cord following the induction of lung injury by an endotracheal injection of bleomycin in C57BL/6 mice. This protocol can be easily extended to the preclinical testing of other therapeutics.

Streszczenie

Pulmonary fibrosis is a hallmark of several human lung diseases with a different etiology. Since current therapies are rather limited, mouse models continue to be an essential tool for developing new antifibrotic strategies. Here we provide an effective method to investigate in vivo antifibrotic activity of human mesenchymal stromal cells obtained from whole umbilical cord (hUC-MSC) in attenuating bleomycin-induced lung injury. C57BL/6 mice receive a single endotracheal injection of bleomycin (1.5 U/kg body weight) followed by a double infusion of hUC-MSC (2.5 x 10⁵) into the tail vein, 24 h and 7 days after the bleomycin administration. Upon sacrifice at days 8, 14, or 21, inflammatory and fibrotic changes, collagen content, and hUC-MSC presence in explanted lung tissue are analyzed. The injection of bleomycin into the mouse trachea allows the direct targeting of the lungs, leading to extensive pulmonary inflammation and fibrosis. The systemic administration of a double dose of hUC-MSC results in the early blunting of the bleomycin-induced lung injury. Intravenously infused hUC-MSC are transiently engrafted into the mouse lungs, where they exert their anti-inflammatory and antifibrotic activity. In conclusion, this protocol has been successfully applied for the preclinical testing of hUC-MSC in an experimental mouse model of human pulmonary fibrosis. However, this technique can be easily extended both to study the effect of different endotracheally administered substances on the pathophysiology of the lungs and to validate new anti-inflammatory and antifibrotic systemic therapies.

Wprowadzenie

Pulmonary fibrosis is a progressive pathological process characterized by the excessive deposition of extracellular matrix components, mainly type I collagen, in the lung interstitium, leading to impaired lung function. It is the hallmark of several human lung diseases with a different etiology and represents a poor clinical prognostic factor. Since current therapies are rather limited¹, mouse models continue to be an essential tool both for the further investigation of the pathogenic mechanisms influencing the onset and the progression of the disease and for developing new antifibrotic strategies^2,3.

To date, the administration of bleomycin has been the most commonly applied model of experimentally induced pulmonary fibrosis⁴. Beside multiple delivering methods (including intravenous, intraperitoneal, subcutaneous, and inhalational), intratracheal or endotracheal injections of bleomycin have emerged as the most frequently used routes^4,5. The method that we describe herein has been developed to avoid the scalding effect of bleomycin on the tracheal mucosa. In fact, by exteriorizing the trachea and visualizing it through an operating microscope, it is possible to achieve the instillation of the entire volume of bleomycin solution directly into the lower airway without any spills in the upper airway. When the required surgical expertise and instrumentation are available, this method allows for the safe, robust, and reproducible induction of lung inflammation and fibrosis, as reported below.

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Protokół

All animal care and experimental procedures were approved by the Italian Ministry of Health (authorization n. 456/2016-PR) and performed according to the Declaration of Helsinki conventions.

1. Mice

1. After purchasing them, allow the mice to acclimate for at least 7 days before the injection.
   NOTE: Mice were housed in the animal facility under pathogen-free conditions, were maintained under constant temperature and humidity on a 12 h light/dark cycle, and were given free access to water and standard pellet food.
2. Use female C57BL/6 mice and inject them at 12 to 16 weeks of age.

2. Endotracheal injection of bleomycin

1. Bleomycin preparation
   CAUTION: Based on the Globally Harmonized System of Classification and Labelling of Chemicals (GHS), bleomycin is classified as a GHS08 health hazard.
   1. Prepare bleomycin under a chemical hood.
   2. To obtain the desired working concentration (0.05 U/100 µL), resuspend 15 U of lyophilized bleomycin sulfate in 30 mL of sterile saline.
   3. Carefully mix the sample by inverting the tube to avoid clot formation.
   4. Properly label the tube with the date of resuspension, store it at 4 °C, and use its content within 24 h.
   5. Prior to the instillation, equilibrate the bleomycin solution to room temperature.
      NOTE: In this experiment, a single dose of 1.5 U/kg body weight of bleomycin was used to induce lung injury in C57BL/6 mice. Nevertheless, each mouse strain has a different sensitivity to bleomycin^6,7. Titration of bleomycin should be performed to determine the optimal dose in the mouse strain used for the experiments.
2. Anesthesia
   1. Prepare anesthesia by dissolving 0.2 g of 2,2,2-tribromoethanol in 9 mL of sterile saline and 1 mL of absolute ethanol (at a working concentration of 20 mg/mL).
   2. Mix thoroughly by inverting the tube to avoid clot formation.
   3. Properly label the tube with the date of preparation, store it at 4 °C in darkness, and use it within 3 days.
   4. Anesthetize the mice with an intraperitoneal injection of 250 µL of tribromoethanol solution (at a final dose of 200 mg/kg body weight) per mouse, using a 1 mL syringe and a 26 G needle.
      NOTE: With this dose, the mice are unconscious for at least 20 min. When necessary, adjust the dosage according to the mouse response, in consultation with the veterinarian.
   5. Monitor the mouse breathing. The respiration rate will slightly slow down. After a few minutes, pinch one of the mouse feet to check the lack of pedal reflex.
3. Endotracheal injection
   1. Maintain aseptic conditions during all the procedure. Use sterile surgical instruments and materials, wear sterile gloves and avoid contact with any non-sterile surface.
   2. Lie down the anesthetized mouse on its back on a surgical platform and hold it in place by delicately fixing its legs with surgical tape strips.
      NOTE: Gentle taping of mouse legs is recommended to avoid mouse sliding away from the surgical platform during its rotation (step 2.3.10).
   3. Place the mouse on heated mat to keep the rectal temperature stable at 37 °C throughout the intervention. Measure the rectal temperature by a rectal probe.
   4. Gently hyperextend the mouse neck by placing a “pillow”, for example, a dental cotton roll, beneath its cervical region.
   5. Gently shave the throat with a razor blade.
   6. Remove hair from the surgical area with alcohol and disinfect the mouse skin several times with 1% povidone-iodine solution.
   7. Pinch the skin with a pair of anatomical forceps and make a short incision in correspondence of the mouse sternohyoid muscle, using a pair of ring-handled, curved blunt scissors.
      NOTE: The incision of the skin is about 0.5 cm in length. The corresponding skin piece which is removed is so small that it will create no tension in the mouse neck.
   8. Stop the bleeding with cotton wool sticks.
   9. Exteriorize the trachea by blunt dissection, gently cleaning it from fat and other tissues.
   10. Rotate the surgical platform to orient the mouse with its head toward the operator.
       NOTE: This position allows the operator, during the injection, to angle the syringe so that it follows the natural path of the trachea straight to the lungs.
   11. Place the mouse under an operating microscope to help with the visualization of the trachea. Adjust the illumination and set the magnification (between 1 and 1.2), focus, and sharpness. The trachea can be easily distinguished as a white translucent tube, and the tracheal rings are clearly visible.
   12. Mix the bleomycin solution by gently pipetting, and aspirate 100 µL into a 0.5 mL syringe with a 25 G needle, avoiding bubble formation.
   13. Once the trachea in clearly visualized, carefully puncture it with the needle tip at an angle of 30° (Figure 1A).
   14. Slowly instill 100 µL of bleomycin or sterile saline (vehicle control) directly into the lumen of the trachea. Wait a few seconds until the entire volume travels down the needle, and then remove it from the trachea.
   15. Observe a few seconds of apnea, which occurs when the needle is correctly inserted into the trachea so that the mouse will immediately inhale the entire volume of the liquid.
   16. If the mouse is not inhaling the liquid, carefully monitor its breathing and adjust the needle position. If the mouse stops breathing, immediately remove the needle and allow the mouse to resume breathing normally before reinserting it.
   17. Safely discard the syringe and needle after the injection.
   18. Close the subcutaneous fascia and the skin wound with a 5-0 absorbable suture.
       NOTE: When not completely reabsorbed, remove sutures 7-10 days post-surgery.
4. Animal recovery
   1. Place the injected mouse on its side on a heating pad for recovery.
   2. Monitor the mouse breathing and observe the mouse until it starts moving and regains sternal recumbency and full consciousness.
   3. Once it is confirmed that the mouse is in good condition, return it to the original cage. Do not return it to the company of other animals until it has fully recovered.
   4. To ensure prolonged analgesia and avoid any residual post-interventional pain, administer subcutaneously buprenorphine (at a final dose of 0.05 mg/kg body weight) to mouse every 12 h post endotracheal injection.
   5. Examine the mice for 24 h after the endotracheal injection of bleomycin and do so twice a day. Monitor the mice for respiratory distress, weight loss, behavior abnormalities, and for any sign of morbidity.

3. Tail vein infusion of human umbilical cord mesenchymal stromal cells

1. Cell preparation
   NOTE: The isolation, characterization, and cultivation of mesenchymal stromal cells from human umbilical cord has previously been described^8,9,10. hUC-MSC should be aseptically manipulated and infused; therefore, perform all steps under a sterile hood.
   1. Expand the hUC-MSC in 75 cm² culture flasks to early passages (1–3 maximum).
      NOTE: The hUC-MSC should be 70% confluent at the day of their infusion into mice.
   2. Wash the cells with 10 mL of sterile phosphate-buffered saline (PBS) at room temperature.
   3. Add 2 mL of trypsin and incubate the cells at 37 °C for about 1 min, until they start detaching.
   4. Neutralize the trypsin by adding 8 mL of hUC-MSC complete medium containing 10% fetal bovine serum (FBS).
   5. Collect the cells by centrifugation at 350 x g for 10 min.
   6. Resuspend the pellet in sterile saline and count the cells using a Bürker chamber. Prepare the cell suspension for infusion by diluting the cells to a final concentration of 2.5 x 10⁵ in 200 µL of sterile saline per mouse. Prepare an excess cell suspension to ensure there is enough volume for infusing all mice.
   7. Keep the cells on ice prior to the infusion. Infuse within a few hours, as described in section 3.3.
2. Anesthesia
   NOTE: In order to minimize the risk of damaging the mouse tail vein during injection the mouse must not move. Therefore anesthesia has been preferred over simple mouse restraining.
   1. Anesthetize the mice by 4% isoflurane inhalation in an induction chamber.
   2. Monitor the mouse breathing. The respiration rate will slightly slow down. After a few minutes, pinch one of the mouse feet to check for proper anesthetization.
3. Tail vein infusion
   1. Once unconsciousness has been confirmed, place the mouse under a sterile hood for the aseptic hUC-MSC intravenous infusion.
   2. Maintain general anesthesia throughout the experiment via a facial mask with a continuous flow of 1.5% isoflurane.
   3. To promote vasodilation and allow for an easier injection, soak the mouse tail in warm water for 2 min.
   4. Mix the cell suspension by gently pipetting to make sure that the cells do not form clumps. Aspirate 200 µL into a 1 mL syringe with a 26 G needle, avoiding bubble formation.
   5. Hold the mouse tail by the tip and gently straighten it.
   6. Locate the lateral vein of the mouse tail; gently scrape it with a scalpel and wipe it with 70% ethanol.
      NOTE: Gently scraping of the tail is performed to remove hair, making the site of injection smoother and cleaner.
   7. Starting from the distal portion of the tail, insert the needle into the vein at a 15° angle and slowly infuse 200 µL of hUC-MSC or sterile saline (vehicle control) (Figure 1B).
   8. Monitor the successful intravenous infusion by the liquid entering the vein without resistance and by a lack of extravasation. Wait a few seconds until the entire volume travels down the needle, and then remove it from the vein.
   9. To prevent bleeding, briefly apply pressure to the entry wound with a sterile gauze.
   10. Safely discard the syringe and the needle after the infusion.
4. Animal recovery
   1. Place the infused mouse on its side on a heating pad for recovery.
   2. Monitor the mouse breathing and observe the mouse until it starts moving and regains sternal recumbency and full consciousness.
   3. Once it is confirmed that the mouse is in good condition, return it to the original cage. Do not return it to the company of other animals until it has fully recovered.
   4. Examine the mice for 24 h after the tail vein infusion and every other day, to monitor their health status and detect any suffering or pathological sign early.

4. Organ explant and tissue processing

1. Sacrifice the mice at days 8, 14, or 21 after the bleomycin administration (Figure 1C) by overdose of injectable anesthetic.
2. Excise the trachea and the lungs and immediately wash them in ice-cold PBS.
3. Snap-freeze the right lungs in liquid nitrogen and store them at -80 °C for a subsequent molecular analysis¹⁰.
4. Inflate the left lungs with 4% paraformaldehyde and fix them in 10% neutral-buffered formalin solution for 24 h; then, dehydrate them in graded alcohol series, clear them in xylene, and embed them in paraffin¹⁰.

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Wyniki

Lung injury was induced by a single endotracheal injection of 1.5 U/kg body weight of bleomycin sulfate in 100 µL of sterile saline. Control animals received an endotracheal injection of an equal volume of saline. Two shots of hUC-MSC (2.5 x 10⁵ in 200 µL of sterile saline) were infused into the mouse tail vein, 24 h and 7 days after the bleomycin administration. Control animals received an intravenous infusion of an equal volume of sterile saline. Mice were sacrificed for lu...

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Dyskusje

Endotracheal administration is the preferential route for delivering exogenous agents into the lungs. Since several years, the direct injection of bleomycin into the trachea has been widely used to induce pulmonary fibrosis¹³ and, recently, more advanced, noninvasive techniques have been developed to accomplish this^14,15,16.

The method described here provides several meaningful...

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Materiały

Name	Company	Catalog Number	Comments
C57BL/6 mice	Charles River	Jax Mice Stock n. 000664
2,2,2-Tribromoethanol (Avertin)	Sigma-Aldrich	T48402
Barraquer Micro Needle Holder	Lawton	62-3755
Bleomycin sulfate	Sigma-Aldrich	B1141000
Bürker chamber	Brand	718905
Culture Flasks	EuroClone	ET7076
Disposable razors	Unigloves	4080
Dissecting Forceps	Aesculap Surgical Instruments	BD311R
DPBS	Gibco	14190-144
Heating pad	2Biological Instruments	557023
Isoflurane Vet	Merial Italia	N01AB06
Operating Microscope	Carl Zeiss	Model OPM 16
TrypLE Select Enzyme	Gibco	12563-029
Vannas Micro Scissors	Aesculap Surgical Instruments	OC498R
Vicryl Plus 4/0 Absorbable Suture, FS-2 needle 19 mm	Ethicon	VCP392ZH