Precision Cut Lung Slices as an Efficient Tool for Ex vivo Pulmonary Vessel Structure and Contractility Studies

Summary

Presented here is a protocol for preserving the vascular contractility of PCLS murine lung tissue, resulting in a sophisticated three-dimensional image of the pulmonary vasculature and airway, which can be preserved for up to 10 days that is susceptible to numerous procedures.

Abstract

The visualization of murine lung tissue provides valuable structural and cellular information regarding the underlying airway and vasculature. However, the preservation of pulmonary vessels that truly represents physiological conditions still presents challenges. In addition, the delicate configuration of murine lungs result in technical challenges preparing samples for high-quality images that preserve both cellular composition and architecture. Similarly, cellular contractility assays can be performed to study the potential of cells to respond to vasoconstrictors in vitro, but these assays do not reproduce the complex environment of the intact lung. In contrast to these technical issues, the precision-cut lung slice (PCLS) method can be applied as an efficient alternative to visualize lung tissue in three dimensions without regional bias and serve as a live surrogate contractility model for up to 10 days. Tissue prepared using PCLS has preserved structure and spatial orientation, making it ideal to study disease processes ex vivo. The location of endogenous tdTomato-labeled cells in PCLS harvested from an inducible tdTomato reporter murine model can be successfully visualized by confocal microscopy. After exposure to vasoconstrictors, PCLS demonstrates the preservation of both vessel contractility and lung structure, which can be captured by a time-lapse module. In combination with the other procedures, such as western blot and RNA analysis, PCLS can contribute to the comprehensive understanding of signaling cascades that underlie a wide variety of disorders and lead to a better understanding of the pathophysiology in pulmonary vascular diseases.

Introduction

Advances in the preparation and imaging of lung tissue that preserves cellular components without sacrificing anatomical structure provide a detailed understanding of pulmonary diseases. The ability to identify proteins, RNA, and other biological compounds while maintaining physiological structure offers vital information on the spatial arrangement of cells that can broaden the understanding of the pathophysiology in numerous pulmonary diseases. These detailed images can lead to a better understanding of pulmonary vascular diseases, such as pulmonary artery hypertension, when applied to animal models, potentially leading to improved therapeutic strategies.

Despite advances in technology, obtaining high-quality images of murine lung tissue remains a challenge. The respiratory cycle is driven by a negative intrathoracic pressure generated during inhalation¹. When traditionally obtaining biopsies and preparing lung samples for imaging, the negative pressure gradient is lost resulting in the collapse of the airway and vasculature, which no longer represents itself in its present state. To achieve realistic images reflective of current conditions, the pulmonary airways must be reinflated, and the vasculature perfused, changing the dynamic lung into a static fixture. The application of these distinct techniques allows preservation of structural integrity, pulmonary vasculature, and cellular components, including immune cells such as macrophages, allowing lung tissue to be viewed as close to its physiological state as possible.

Precision cut lung slicing (PCLS) is an ideal tool for studying the anatomy and physiology of pulmonary vasculature². PCLS provides detailed imaging of the lung tissue in three dimensions while preserving structural and cellular components. PCLS has been used in animal and human models to allow for live, high-resolution images of cellular functions in three dimensions, making it an ideal tool to study potential therapeutic targets, measure small airway contraction and study the pathophysiology of chronic lung diseases such as COPD, ILD, and lung cancer³. Using similar techniques, the exposure of PCLS samples to vasoconstrictors can preserve lung structure and vessel contractility, replicating in vitro conditions. Along with preserving contractility, prepared samples can undergo additional analysis such as RNA sequencing, Western blot, and flow cytometry when prepared correctly. Finally, reporter color labeled cells marked with tdTomato fluorescence after lung harvest can preserve labeling after preparing microslices, making it ideal for cell tracking studies. The integration of these techniques provides a sophisticated model preserving the spatial arrangement of cells and vessel contractility that can lead to a more detailed understanding of the signaling cascades and potential therapeutic options in pulmonary vasculature disease.

In this manuscript, PCLS murine lung tissue is exposed to vasoconstrictors, demonstrating preserved structural integrity and vessel contractility. The study demonstrates that the tissue prepared and handled appropriately can remain viable for 10 days. The study also demonstrates the preservation of cells with endogenous fluorescence (tdTomato), allowing samples to provide high-resolution images of the pulmonary vasculature and architecture. Finally, ways to handle and prepare tissue slices for RNA measurement and Western blot to investigate underlying mechanisms have been described.

Protocol

All animal care was in accordance with the guidelines of Boston Children's Hospital and the Institutional Animal Care and Use Committee approved protocols. The mice used in this study are wild type C57/B6 mice and Cdh5-CreERT2 x Ai14 tdTomato crossed mice.

1. Preparation of solutions

1. Prepare phosphate buffer solution (1x PBS) and 2% agarose solution required during the experiment in advance.
   1. Mix 2 g agarose powder into 100 mL of autoclaved water. Heat it in the microwave a few seconds at a time until the solution is clear.
   2. Place the solution in a water bath at 42 °C until use.
      ​NOTE: Both PBS and 2% agarose can be stored at room temperature for weeks.

2. Extraction of the mouse lung

1. Euthanize the mouse by isoflurane overdose. Achieve isoflurane overdose by placing a small amount of isoflurane on tissue paper in the lower level and placing the mouse in the upper level in a desiccator. The mouse remains in the desiccator until unconscious.
2. Ensure death of the mouse by applying inferior pressure on the neck and pulling caudal on the tail. Bring the mouse to the dissecting surface.
3. Place the mouse in the supine position and secure it into place taping paws and nose to table with adhesive tape.
4. Spray the ventral surface of the mouse with 70% ethanol and wipe off the excess ethanol.
5. Lift the abdominal skin of the mouse with forceps at the location of the bladder and cut at the midline with surgical scissors, moving superiorly to the cervical region, exposing the trachea.
6. Lift the underlying fascial layer with tweezers and cut with surgical scissors to expose visceral organs and mediastinal compartment, again cutting inferiorly to superior.
7. Cut the sternum at the midline to expose the heart and the lung.
8. Using blunt dissection, detach the diaphragm from the liver and abdominal compartment.
9. Locate the inferior vena cava (IVC) under the intestines and cut the IVC.
10. Locate the right ventricle.
    NOTE: The right ventricle will have a lighter appearance compared to the left ventricle and the intraventricular septum should be visualized, separating the right ventricle from the left ventricle.
11. Inject 0.5 mL of 1% fractionated heparin to the right ventricle with a 25-30 G butterfly needle and then flush slowly but steadily with 10-15 mL of 1x PBS (Figure 1A).
    1. Use caution not to insert the needle through the heart and inject heparin into the mediastinal cavity.
       NOTE: The injection of 1x PBS turns the lung tissue white. The fluid extravasating from the abdominal aorta should be clear and colorless and the liver may become white in appearance after successful flushing.
12. Locate the larynx and dissect the surrounding fascia and tissue using blunt tip tweezers.
13. Place the surgical suture under the trachea and loosely tie a surgical knot.
14. Place a small hole in the trachea superior to string and canulate with 20 G blunt-ended needle.
15. Tighten the suture around the needle and trachea using a surgical knot.
16. Inject 2.5-4 mL of agarose into the trachea and monitor for inflation of the lung.
17. After agarose is instilled, pour cold, chilled 1x PBS over the lung to solidify agarose.
18. Cut the trachea superior to surgical suture and dissect the lung and heart from the mediastinum by removing any adhesions and fascia.
19. After solidification, place in 1x DMEM (enough to submerge tissue) in a Petri dish to keep on ice. Immediately slice one lobe using a vibratome machine (Figure 1B).

3. Precision cut lung slices

1. Attach the sample to the platform with superglue, keeping the medial side of the sample facing up.
2. Fill the sample container with 1x PBS, ensuring that the sample is completely submerged.
3. Fill the container surrounding the sample container with ice to keep surrounding PBS and sample cold.
4. Turn on the vibratome and adjust to the desired settings below.
   1. Set the thickness to 300um.
   2. Set the frequency to 100 Hz.
   3. Set the amplitude to 0.6 mm.
   4. Set the speed to 5 µm/s.
5. Using an Allen wrench, turn the blade holder into the safe position and open the jaws to insert a blade.
6. Tighten the jaws with an Allen wrench and turn the blade holder into the appropriate position for slicing.
7. Place the sample and the platform onto the box and slide in front of the blade.
8. Fill the box around the sample platform with 1x PBS until the sample is submerged.
9. Bring the vibratome blade up to the edge of the block and manually lower the blade until it is even with the top of the sample.
10. Confirm the appropriate settings and run the vibratome (Figure 2).
11. As fresh slices are cut, remove the samples from the PBS and place them into a sterile Petri dish with 10 mL of 1x DMEM containing 1x antibiotic-antimycotic.
12. When finished, retract the blade entirely and then use the Allen wrench to raise the blade into a safe position.
13. Store the samples in 1x DMEM in an incubator at 37 °C with viability preserved for up to 10 days (see viability experiment below).

4. Example vasoconstrictor experiment

1. Place a vibratome slice on a microscope slide.
2. Before placing it on the slide, use a cleaning wipe to get rid of the excess medium (PBS).
3. Place the sample under phase-contrast microscopy and use 10-20x magnification to identify a vessel.
4. Put 500 µL of vasoconstrictors, such as 60 mM KCl or 1 µM Endothelin-1 to completely submerge the slide.
5. Observe and capture the video by recording for 30 s-60 s (Video 1).

5. Preparing the tissue for RNA or protein lysis on PCLS

1. Before beginning the experiment, fill a small polystyrene foam box with 1 L of liquid nitrogen.
2. Place two small microcentrifuge tubes (1.5 mL) in the container with liquid nitrogen before starting.
   NOTE: Liquid nitrogen should cool outside of the tubes, however, not be inside. Be sure to handle liquid nitrogen with care and do not expose the skin to liquid nitrogen. Use forceps and gloves to place and remove tubes from the box.
3. Place 4-5 fresh vibratome slices in a mortar bowl.
4. Pour 5-10 mL of liquid N2 on top of the slices in the mortar bowl.
5. Quickly use the pestle to grind the flash freeze slices into powder before liquid nitrogen evaporates.
   NOTE: Tissue should condense into a fine powder. If not, add additional liquid nitrogen until achieved.
6. Using a steel laboratory scooper (prechilled with liquid nitrogen), scoop the powder into the two chilled microcentrifuge tubes.
7. Lyse the powder by adding 500 µL of RNA extraction reagent to proceed with RNA isolation or 500 µL of RIPA buffer (contains 1x protease inhibitors) to proceed with protein lysis.
8. Store the samples at -80 °C until additional RNA isolation, BCA measurement, and western blot.

6. Determining viability

1. After vibratome preparation, place two lung slices into a 24-well culture plate with 450 µL of DMEM media and 50 µL of cell viability reagent (ensure that the tissue is submerged entirely).
2. Place the samples back into 5% CO₂ at 37 °C incubator overnight with minimal exposure to light.
3. In the morning, observe the solution for color change. The blue solution turns pink when the tissue is viable.

7. Preservation of cell labeling

1. Treat a transgenic Cdh5-CreERT2 crossed with Ai14 tdTomato mouse with an IP injection of Tamoxifen (2 mg/day) for a total of 5 days (total dose 10 mg Tamoxifen) to induce tdTomato label Cre positive cells.
2. One week after injection, prepare the lungs using the above steps 1 to 3.
3. After preparation of the precision-cut lung slice, place the tissue onto a microscope slide and place a coverslip on top of the tissue.
4. Use a confocal microscope to detect tdTomato staining (using excitation wavelength 555 nm).

Results

When added to cells or tissue, the viability reagent is modified by the reducing environment of viable tissue and turns pink/red, becoming highly fluorescent. The representative color changes detected from day 0-1 and day 9-10 are demonstrated in Figure 3. As noted, the solution started blue and turned pink overnight, demonstrating viability. Color change typically occurs within 1-4 h; however, a longer time may be necessary. To assay for viability, a plate reader was used to determine the a...

Discussion

In this manuscript, an enhanced method to produce high-resolution images of murine lung tissue that preserves the vascular structure and optimizes experimental flexibility is described, specifically using the application of PCLS to obtain microslices of lung tissue that can be viewed in three dimensions with preserved contractility of the vasculature. Using the viability reagent, the protocol demonstrates that carefully prepared and preserved slices can retain viability for more than a week. Preserved viability of the mi...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
0.5cc of fractionated heparin in syringe	BD	100 USP units per mL
1X PBS	Corning	21-040-CM
20 1/2 inch gauge blunt end needle for trachea cannulation	Cml Supply	90120050D
30cc syringe	BD	309650
Anti Anti solution	Gibco	15240096
Automated vibrating blade microtome	Leica	VT1200S
Cell Viability Reagent (alamarBlue)	Thermofisher	DAL1025
Confocal	Zeiss	880
Dulbecco’s Modified Eagle Medium and GLutaMAX, supplemented with 10% FBS, 1% Pen/Strep	Gibco	10569-010
Endothelin-1	Sigma	E7764
KCl	Sigma	7447-40-7
Mortar and Pestle	Amazon
RIPA lysis and extraction buffer	Thermoscientific	89900
Surgical suture 6/0	FST	18020-60
TRIzol Reagent	Invitrogen, Thermofisher	15596026
UltraPure Low Melting Point Agarose	Invitrogen	16520050
Vibratome	Leica Biosystems	VT1200 S
Winged blood collection set (Butterfly needle) 25-30G	BD	25-30G