Generation of Human 3D Lung Tissue Cultures (3D-LTCs) for Disease Modeling

* These authors contributed equally
Medicine
 

Summary

Here, we present a protocol for the preparation of agarose-filled human precision-cut lung slices from resected patient tissue that are suitable for generating 3D lung tissue cultures to model human lung diseases in biological and biomedical studies.

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Gerckens, M., Alsafadi, H. N., Wagner, D. E., Lindner, M., Burgstaller, G., Königshoff, M. Generation of Human 3D Lung Tissue Cultures (3D-LTCs) for Disease Modeling. J. Vis. Exp. (144), e58437, doi:10.3791/58437 (2019).

Abstract

Translation of novel discoveries to human disease is limited by the availability of human tissue-based models of disease. Precision-cut lung slices (PCLS) used as 3D lung tissue cultures (3D-LTCs) represent an elegant and biologically highly relevant 3D cell culture model, which highly resemble in situ tissue due to their complexity, biomechanics and molecular composition. Tissue slicing is widely applied in various animal models. 3D-LTCs derived from human PCLS can be used to analyze responses to novel drugs, which might further help to better understand the mechanisms and functional effects of drugs in human tissue. The preparation of PCLS from surgically resected lung tissue samples of patients, who experienced lung lobectomy, increases the accessibility of diseased and peritumoral tissue. Here, we describe a detailed protocol for the generation of human PCLS from surgically resected soft-elastic patient lung tissue. Agarose was introduced into the bronchoalveolar space of the resectates, thus preserving lung structure and increasing the tissue's stiffness, which is crucial for subsequent slicing. 500 µm thick slices were prepared from the tissue block with a vibratome. Biopsy punches taken from PCLS ensure comparable tissue sample sizes and further increase the amount of tissue samples. The generated lung tissue cultures can be applied in a variety of studies in human lung biology, including the pathophysiology and mechanisms of different diseases, such as fibrotic processes at its best at (sub-)cellular levels. The highest benefit of the 3D-LTC ex vivo model is its close representation of the in situ human lung in respect of 3D tissue architecture, cell type diversity and lung anatomy as well as the potential for assessment of tissue from individual patients, which is relevant to further develop novel strategies for precision medicine.

Introduction

Chronic and acute lung diseases are a major cause of morbidity and mortality worldwide1. For patients with chronic lung diseases like obstructive pulmonary disease (COPD)2, severe asthma3, lung cancer4 and diffuse parenchymal lung diseases5, curative therapies are currently not available. Although studies in animal models for lung diseases have deepened the understanding of disease pathomechanisms6 and have led to the identification of potential novel therapeutic targets7,8,9, these models exhibit relevant biological and physiological differences when compared to humans10. To overcome these discrepancies between murine and human biology as well as anatomy, human ex vivo 3D lung tissue culture (3D-LTC) systems are used in various areas of biomedical research. These 3D-LTC culture systems are based on precision-cut lung slices (PCLS). The generation of PCLS ex vivo allows analysis of a third spatial dimensionality, which allows for the investigation of the spatial and functional relationships of cells in entire alveoli and airways11, as well as the interstitium, vasculature and mesothelium. Notably, PCLS ex vivo models are multicellular, meaning that they contain most functional cells of in situ lungs, thus closely representing the cells' native biological environment and thus overcoming the limited cell-cell and cell-matrix interaction in most 2D cell culture approaches. Up to now, ex vivo murine PCLS were used to model pulmonary diseases, like COPD12, lung fibrosis13, lung cancer14, viral infection15,16, bronchopulmonary dysplasia17, and asthma18. However, a considerable proportion of novel drug therapies in human lung diseases that were investigated in clinical trials do not translate to the clinic due to their lack of efficacy or safety, assumingly due to yet considerable differences between human and murine biology and disease19,20,21.

Over several years, human PCLS have been largely used to assess lung toxicity of chemicals and drugs. Only recently, human lung tissue has been used from patients with COPD22,23, asthma24, and lung fibrosis25, to pursue pathophysiological and pharmacological studies. By using resected patient organ material and generating PCLS thereof, one can recapitulate major disease hallmarks in a complex 3D tissue environment22 representing and maintaining most of the native cellular diversity of the organ. Moreover, diseased tissue applied in a variety of experimental setups was shown to mimic disease-like changes in liver, intestine and kidney26,27,28,29.

However, processing of lung tissue remains challenging for several reasons. Unlike solid tissue, native lung parenchyma tends to collapse without ventilation and exhibits lower tissue stiffness. These properties impede the slicing of the tissue. Thus, filling of airways and the alveolar space with low-melting point agarose preserves the native lung structure and provides the stiffness needed for precision-cut slicing of murine and human lungs30. Human lung resectates donated for research purposes are by their nature anatomically, genetically and physiologically highly diverse, thus often presenting a high inter-patient variability when performing experiments25. In contrast to the whole lobe or whole lung explants, lung samples resected by means of thoracic surgery do not necessarily follow the anatomical segments and, therefore, require special preparation. In this article, we provide a detailed and optimized protocol for the generation of human PCLS from resected lung tissue and their subsequent cultivation and experimental use to model lung disease.

Protocol

The use of human tissue was approved by the ethics committee of the Ludwig-Maximillian University [Munich, Germany (project number 455-12)]. Tumor-free human lung resections were provided by the Asklepios Biobank for Lung Diseases (Gauting, Germany, project number 333-10).

NOTE: All procedures of human PCLS production (Figure 1) are done under a sterile laminar flow hood.

1. Preparation of Instruments and Materials

  1. Prepare all materials for the inflation of lung tissue with agarose as described below.
    1. Prepare the cultivation medium: Dulbecco’s Modified Eagle Medium (DMEM) F-12 supplemented with L-Glutamine, HEPES, 10,000 IE Penicillin, 10,000 IE Streptomycin and 0.1% (v/v) fetal bovine serum.
      NOTE: Medium is used at 37 °C.
    2. Prepare a sterile metal tray covered with tissue paper. Place a sterile 15 cm cell culture dish on the tray.
    3. Fill the cell culture dish with the 15 mL of cultivation medium.
    4. Prepare a 3% (w/v) agarose solution by dissolving the appropriate amount of low-melting point agarose in a minimum of 30 mL of cultivation medium.
    5. Heat the solution in a microwave until boiling. Cool the agarose solution to 42 °C in a water bath. Keep the liquid agarose solution stored in the water bath.
    6. Prepare several 50 mL conical tubes filled with the liquid agarose.

2. Resected Lung Tissue

  1. Store fresh tumor free lung tissue of lobectomy resectates immediately after resection in DMEM F-12 medium at 4 °C until step 3.
  2. Do not exceed cold ischemia time of 4-8 h prior to processing.

3. Inspection and Selection of Resected Tissue Prior to Agarose Filling

  1. Lift the tissue from the medium with tweezers. In order to avoid any damage to the tissue, especially to the pleura, handle the tissue with tweezers at the airways only.
  2. Score the tissue quality by criteria of the Lung Agarose Filling Score defined in Table 1.
  3. Proceed to step 4 if the tissue’s quality is scored above or equal to 72. If the tissue’s quality is scored below 60, do not continue further with agarose filling.
    NOTE: If the tissue score is between 60 and 68, the agarose-filling and tissue slicing still might produce reasonable results, and a final decision for prolongation of the experiment has to be made case to case. However, lung tissue that did not meet the above-mentioned requirements, mostly fails in agarose filling.

4. Lung Tissue Inflation by Agarose Filling

  1. Lift the tissue from the storage medium and drain excess media from the tissue. Transfer the lung tissue into the 15 cm culture dish prepared in 1.1.2.
  2. Fill a 30 mL syringe with the low-melting point agarose from 1.1.3.
  3. Prepare a peripheral venous catheter by removing the obturator and attach it to a 30 mL syringe
  4. Identify a bronchus (0.5-3 mm in diameter) in the tissue that is ventilating an intact section of the tissue (see Figure 2).
  5. Insert the cannula into the selected bronchus (0.5-3 mm diameter).
  6. Gently push the cannula gently forward as far as possible.
  7. Seal the bronchus around the cannula by compressing the bronchial wall around the cannula with forceps, ideally clamping any adjacent pulmonary artery at the same time.
  8. Occlude other additional airways with a surgical clamp to prevent agarose leaking through these airways.
  9. Lift the tissue with the forceps from the culture dish.
  10. Manually pour the agarose with the syringe no faster than 0.3 mL/s. The speed of agarose filling might vary between approximately 0.05 and 0.3 mL/s due to the heterogeneous resistance of airways and/or atelectasis.
  11. If high resistance while filling or agarose leaking from the tissue is observed, retry the whole procedure with a different bronchus from step 4.4. Perform troubleshooting as described below.
    NOTE: The degree of agarose filling is highly dependent on the position of the catheter in the tissue and deep penetration of the catheter results in agarose filling of small cone like regions (*) of the lung tissue (Figure 2C).
    1. In case of high resistance, try positioning of the catheter leads to proper filling of most regions of the tissue (#) (Figure 2D).
    2. As plugs of early solidified agarose in the proximal bronchi or other airway obstructions (arrow) can lead to an incomplete filling of the tissue (Figure 2E), do not force agarose filling as this might lead to defects in the filled area, but not in a filling of the obstructed tissue parts.
    3. If the respiratory tree derived from the cannulated bronchus is damaged during resection and the agarose filling results in a constant leaking of the liquid agarose (arrow in Figure 2F), insert the catheter into a more peripheral part of the airway system to fill at least a minor part of the tissue (*) (Figure 2G). Additionally, seal the damaged peripheral airway with a surgical clamp (arrow) (Figure 2H).
  12. Apply agarose until the lung tissue is filled completely. Do not over-inflate the tissue as this may cause irreversible damage to the tissue structure and its cells.
  13. Clamp the bronchus that was used for the filling immediately. Remove the cannula prior to clamping.
  14. Incubate the tissue in the culture medium at 4 °C for 30 min to ensure agarose solidification.
  15. If the resected tissue has multiple bronchial entries, repeat step 4.2 to 4.13 until all parts of tissue are filled with agarose.
  16. Store the agarose filled lung tissue sections in 4 °C cold medium until slicing.

5. Precision-cut Lung Slicing

  1. Identify regions in the lung tissue that are solidly filled with the agarose. Solidly filled regions will not collapse when they are gently pressed with tweezers against the bottom of the cell culture dish.
    1. Excise a 1-1.5 cm3 block of regions described in 5.1, whereas one side still should be covered with pleura.
  2. Attach each individual tissue block with the pleural side contacting the holder of the vibratome by using a cyanoacrylate glue.
    NOTE: The pleura is slightly elastic and therefore impedes the cutting with the vibratome blade. Placed on the tissue holder, the pleura will not interfere with the cutting and, importantly, forms a natural barrier between the cyanoacrylate glue and the tissue’s parenchyma allowing for minimal diffusion of the glue.
  3. Slice the lung tissue with the vibratome with the following settings: thickness: 500 µm, frequency: 100 Hz, amplitude of the knife: 1.2 mm, forward speed of the blade of 3-12 µm/s, which depends on tissue stiffness. Reduce the protrusion-speed of the blade if the slice is not cut properly, or if the tissue block itself starts to vibrate.
  4. Gently transfer the slice by lifting it with forceps from the vibratome tray into a well of a 12-well plate filled with cultivation medium. Finally, incubate the lung slices in an incubator under standard cell culture conditions.
  5. Stop slicing when 2-3 mm of the tissue block are left unsliced since the cyanoacrylate glue may have compromised the tissue integrity of this region.

6. Generation of PCLS Punches

  1. Transfer the lung slices from a single well to an empty 10 cm dish.
  2. Place a 4 mm biopsy puncher orthogonally to the upper surface of a PCLS and start to move the puncher in clockwise and counterclockwise rotations.
  3. Fill cell culture medium into the wells of a 96-well plate. Lift the tissue punches with forceps and transfer the punches into the wells of a 96-well plate. Finally, incubate the lung punches submerged in the medium prepared in 1.1.1. in a cell culture incubator under standard conditions (21% (v/v) oxygen, 5% (v/v) carbon dioxide and 95% humidity, at 37 °C).

7. Tissue Culture and Sample Harvesting

  1. Culture the PCLS and punches overnight in an incubator under standard cell culture conditions.
  2. Culture PCLS and punches under outlined condition for a maximum of 120 hours after their generation to ensure cellular viability and function.
  3. For harvesting protein as well as RNA, wash PCLS and punches three times in phosphate buffered saline (PBS), transfer them into cryovials and snap-freeze in liquid nitrogen.
  4. Sample medium supernatant of cultured PCLS punches for the analysis of secreted proteins.
    1. For histological analyses, wash the PCLS and punches three times with PBS and fix them with 4% paraformaldehyde by incubating for 30 min at 37 °C. Finally, store the PCLS in PBS at 4 °C for further downstream staining.

Representative Results

PCLS generation
The generation of PCLS can be separated into four essential steps: surgical lung tissue resection, agarose filling, vibratome-based PCLS generation, and culture of PCLS. The resected lung tissue is filled with low-melting point agarose, which adds the required stiffness to the lung tissue for slicing and preserves the native lung structure and architecture. Of note, PCLS generation is highly time consuming, thus often overnight storage of the filled lung tissue in DMEM F-12 medium can be included as an additional step and PCLS generation is started on the next day. Depending on the following experimental setup, generated PCLS can be incubated overnight in standard cell culture medium containing 0.1% (w/v) fetal bovine serum, before experimental conditions are applied. 3D-LTCs were viable and exhibited cellular functionality (such as surfactant protein secretion) for up to 120 h22 in the culture conditions outlined in this protocol (Figure 1) and might be optimized upon further improvement thereof.

Agarose filling
For agarose filling of the tissue, a cannula of a peripheral venous catheter with a 1.3 mm diameter attached to the agarose-filled syringe was inserted into a bronchus at the surface of the cut tissue (Figure 2A). Bronchi are often localized near to a pulmonary artery. While the arteries have thinner walls and tend to collapse, bronchi exhibited a good visible lumen. Depending on the tissue's integrity, the catheter can be advanced through several generations of the respiratory tree into the periphery of the lung. The penetrated bronchus was sealed around the cannula by using tweezers (Figure 2B). The pulmonary artery can be clamped with the tweezers at the same time. Afterwards, the tissue is lifted up and liquid agarose is gently instilled into the airways.

Depending on the position of the catheter, a majority of the tissue can be filled with liquid agarose (Figure 2D). Optionally, cone like parts of the lung tissue, which reflect the lung's parenchyma ventilated by the penetrated bronchus, might get filled with the agarose (Figure 2C). In both scenarios, a characteristic pattern of solidly filled tissue regions can be observed: first, a major part of the tissue is filled in wedges (Figure 2D), or secondly, smaller protruding round areas of thoroughly filled tissue regions appear (Figure 2C). If parts of the airways obstruct due to agarose clots or other causes, parts of the tissue might not be properly filled with agarose. Thus, only parts of the tissue might be applicable for slicing. In case of leakages during the agarose filling procedure, parts of the filled respiratory tree might get perforated and filling of the lung tissue gets nearly impossible However, possible workarounds include the filling via a more peripheral bronchus, a deeper penetration of the cannula into the distal airways (Figure 2G), or potential clamping of the leakage area (Figure 2H).

Precision-cut lung slicing
Tissue blocks at a length and width of 1-1.5 cm were excised from tissue regions, which were completely filled with solidified agarose (Figure 3A-3B). Next, the individual tissue blocks were glued on the tissue holder of the vibratome (Figure 3C). 500 µm thick PCLS were generated, whereas the tissue block at the vibratome was advancing forward with speeds between 3-12 µm/s. (Figure 3D-3F). Finally, the PCLS were submerged in cell culture medium containing 0.1% (w/v) fetal bovine serum and cultured at standard cell culture conditions, as outlined step 7.

Experimental readouts of human 3D-LTC after 48h of culturing
A representative immunofluorescence staining, as previously described by Alsafadi et al.25, is shown in Figure 4A-4C. Immunolabeling of fibronectin (red) and cell nuclei (DAPI, blue), allowed for imaging of the preserved alveolar structure in the human 3D-LTC ex vivo. Treatment of the human PCLS punches with a profibrotic cytokine cocktail (including transforming growth factor beta 1, platelet derived growth factor AB, lipophosphatidyl acid, and tumor necrosis factor alpha) for 48 h resulted in fibrosis-like changes in human 3D-LTCs. By qPCR, a significant induction of the fibrosis-relevant extracellular matrix components collagen type 1 and fibronectin genes in 3D-LTC punches was observed upon treatment with the profibrotic cocktail (Figure 4D). Additionally, protein levels of the mesenchymal marker vimentin were found upregulated in 3 out of 4 patients after treatment of 3D-LTC punches (Figure 4E).

Figure 1
Figure 1: Workflow of PCLS generation. Tumor-free areas of lung resections are thoroughly inspected due to their tissue integrity. If the tissue is scored suitable for further use (scoring is explained in detail in the material and methods section), it is next filled with liquid agarose. Tissue blocks filled with solidified agarose are subsequently sliced with a vibratome. Submerged in cell culture medium, 3D-LTC are cultured up to 120 h after their generation. Downstream analyses of the 3D-LTCs involve protein- or RNA-expression, live-tissue fluorescence imaging, as well as immunofluorescence staining after fixation of the tissue. Please click here to view a larger version of this figure.

Figure 2
Figure 2: Filling the lung tissue with low-melting point agarose. The lung tissue is cannulated with a peripheral venous catheter which is inserted into a bronchus adjacent to the pulmonary artery (Figure 2A). Tweezers are used to fix the cannula in the bronchus and to clamp the pulmonary artery to avoid leaking of the liquid agarose. Liquid agarose at 42 °C is poured into the lung tissue with a 30 mL syringe (Figure 2B). A distal positioning of the cannula during filling will result in small areas of filled tissue (Figure 2C), while proximal positioning will ensure the filling of a larger tissue volume (Figure 2D). Any obstructions of the airways will reduce the amount of tissue volume that can be filled (Figure 2E). In case of agarose leaking, a distal cannula positioning and/or clamping of the leakage side enables proper agarose filling of the lung tissue (Figure 2F-2H). Please click here to view a larger version of this figure.

Figure 3
Figure 3: Precision-cut lung slicing. A successfully agarose-filled lung tissue is used to excise a piece of a tissue block (1 cm x 1.5 cm x 1 cm) with a scalpel (Figure 3A). Next the excised tissue block is glued to the tissue holder, scale bar indicates 1 cm (Figure 3B). Preferably, the tissue is glued with its pleural surface to the surface of the tissue holder as shown in Figure 3C. 500 µm thick slices are cut by the vibratome with a sapphire knife in a 10°-15° angle relative to the tissue (Figure 3D and 3E). The cutting procedure results in 2-3 cm3 large intact lung slices, Scale bar = 5 mm (Figure 3F). Additionally, by using a biopsy puncher, small reproducible punches with a diameter of 4 mm can be generated. Please click here to view a larger version of this figure.

Figure 4
Figure 4: Experimental readouts of human 3D-LTCs after 48h of culture. A human 3D-LTC punch of 4 mm diameter was immunostained for fibronectin (in red) and DAPI (in blue) (Figure 4A-4C). Scale bars = 1,000 µm. Figure 4C shows the merged image. RNA analysis of PCLS by quantitative RT-PCR shows significant increases of COL1A1 and FN1 gene expression by the profibrotic cocktail25. Figure 4E displays an immunoblot of whole protein lysates of PCLS, which were treated with a fibrotic cocktail25. Probing for Vimentin and β-Actin demonstrated an increased protein expression of the mesenchymal marker (vimentin) after treatment with profibrotic factors in patient samples 1, 3, and 4. Please click here to view a larger version of this figure.

Criterion Points
The tissue sample has intact pleural surface. 20
The tissue sample seems macroscopically intact, lacking incisions, squashing, ruptures and distortions. 20
The tissue sample contains at least one bronchus with a diameter >1mm. 20
The tissue sample contains no or only little amounts of blood. 4
The tissue sample was stored fully in medium and shows no obvious sign of atelectasis. 4
The tissue sample was resected within the last four hours. 4
The tissue sample is larger than 5cm in its largest diameter. 4
Score in sum:

Table 1: Lung Agarose Filling Score. The Lung Agarose Filling Score (LAFS) correlates with the success-rate to fill a tissue resection with agarose for its subsequent vibratome-based PCLS production. The score sums up all points of criteria met by the tissue. An LAFS equal or above 72 predicts good agarose filling properties, a score below 60 predicts a highly probable failure of agarose filling of the tissue.

Discussion

The protocol described in this manuscript covers the generation of PCLS from human lung tissue resectates by filling it with liquid agarose and subsequent vibratome slicing. Generation of tissue slices was demonstrated before for a couple of organs, like liver and brain, whereas the inherent stiffness of these organs allowed direct slicing without any modification of the tissue. Of note, the initial proper preparation of the lung tissue is the most crucial step in generating PCLS. Agarose filling of the lung is the method of choice to stabilize its soft and elastic nature, and to ensure a homogenous and reproducible PCLS generation. Large airways of the resected lung tissue are cannulated to provide access to the small airways, as well as to the intact lung parenchyma. The lack of an intact pleura, which makes agarose filling nearly impossible, is a major reason why lung tissue is mostly not usable for lung slicing. Prospectively, a synthetic pleura originally designed to perform functional experiments on decellularized scaffolds could potentially be applied to achieve successful agarose filling of explants that lack an intact pleura31. Resections resulting in a human lung tissue piece with intact pleura are essential for generating tissue blocks for slicing. Resected tissue is more available due to tumor-free tissue from cancer resections than fully intact lobes or whole-lung explants of patients who underwent lung transplantation.

Commonly, two systems are used to produce PCLS: the Krumdieck tissue slicer15 and vibratory microtomes (vibratomes). Tissue slicers generate slices by passing a tissue block through a metal vessel, which cuts the PCLS at 90° at the end of this vessel. Vibratomes generate PCLS by moving a vibrating knife horizontally over an anchored block of tissue that is submerged in a cooled medium bath, which compared to the Krumdieck slicer exerts less shear force on the tissue. This results in less harsh treatment of the tissue before cultivation. On the other hand, the vibratome cutting is more time and work consuming. In our hands, vibratome slicing enabled the production of a maximum of 100 PCLS or 500 PCLS punches in one day, sufficient for most experimental studies. PCLS can be cultured in various ways: (a) attached to Trans-wells, thus generating an air liquid interface (ALI) system, (b) as dynamic organ culture (DOC), or (c) submerged in cell culture medium at standard cell culture conditions. The in-detail cultivation of PCLS was previously described22,23,25; however, a common standard of cultivation conditions between their usage in various labs around the world is still missing. In particular, the culture time might be critical: as in murine PCLS, a loss of SFTPC positive alveolar type 2 cells is observed after 144 h, but not after 120 h22. In addition, metabolic activity seems to remain stable in murine22 and human PCLS25 for 120 h.

There are a couple of technical limitations for the generation of PCLS: the number and size of the resectates fluctuates over time; the efficiency of the agarose filling, which depends on the presence of intact pleura within the obtained tissue, determines the final success of the PCLS generation; and tissue destruction caused by pathological changes within the obtained (diseased) lung tissue might interfere with the PCLS preparation. Airway obstructions and fibrotic tissue lacking intact alveolar space impede with agarose filling and thus make slicing of the fibrotic tissue a demanding task. Emphysematous tissues as found in diseases such as COPD or alpha-1-anti-trypsin deficiency might not withstand the pressure of agarose filling, and will result in rupture of the alveoli and architectural artefacts. In these cases, the usage of low agarose concentration, e.g., 1% (w/v), might be useful to decrease pressure and speed during agarose filling. Overall, the disease state of the tissue can dramatically limit the use of the tissue for PCLS generation. All these parameters determine the amount of PCLS that can be generated from lung tissue, and also the amount of time it takes to produce the PCLS. Further limitations of PCLS are inconsistencies in between different lung slices with respect to size or tissue content, which requires further normalization steps for experiments. To overcome this, biopsy punches of similar regions of the same slice can be generated. This procedure is apt to reduce the tissue variability and, as an additional benefit, increase the number of PCLS samples that can be used for experiments.

In conclusion, human 3D lung tissue cultures from agarose filled PCLS provide a complex human model for studying lung physiology and diseases. The protocol provides a detailed description of the preparation of PCLS from resected lung tissue and their cultivation, and moreover addresses challenges in agarose filling of human lung resections and how to overcome them.

Disclosures

All authors declare no competing financial interests.

Acknowledgments

The authors are grateful to Marisa Neumann for expert technical assistance. All lung tissues were kindly provided by the CPC-M Bio-Archive. This work was supported by the German Center of Lung Research (DZL), the Helmholtz Association and CPC Research School grants.

Materials

Name Company Catalog Number Comments
Vibratome Hyrax V50 Zeiss -
Hyrax CU 65 Zeiss -
Vasofix Braunüle 18 G B. Braun Melsungen AG 4268130B
30 mL NORM-INJECT Henke Sass Wolf 4830001000
Guarded disposable scalpels, sterile Swann-Morton
Loctite 406 Henkel LOCTITE 406
Synthetic Single Crystal Sapphire Delaware Diamond Knives -
Dulbecco's Modified Eagle Medium F-12 Nutreient Mixture (Ham) + L-Glutamine + 15mM HEPES Gibco 31330-038
Penicillin Streptomycin Gibco by Life Technologies 15070-063
Special process fetal bovine serum (Sera Plus) Pan Biotech P30-3702
Disposable Biopsy Punch pfm medical 48401
96 Well, Black/Clear, Tissue Culture Treated Plate, Flat Bottom with Lid, sterile Falcon / Corning 353219
Agarose, low geling temperature Sigma A9414-100G

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