Recapitulation of the organ-specific microenvironment, which stimulates local angiogenesis, is indispensable for successful regeneration of damaged tissues. This report demonstrates a novel method to implant fibrin gels on the lung surface of living mouse in order to explore how the lung-specific microenvironment modulates angiogenesis and alveolar regeneration in adult mouse.
Recent significant advances in stem cell research and bioengineering techniques have made great progress in utilizing biomaterials to regenerate and repair damage in simple tissues in the orthopedic and periodontal fields. However, attempts to regenerate the structures and functions of more complex three-dimensional (3D) organs such as lungs have not been very successful because the biological processes of organ regeneration have not been well explored. It is becoming clear that angiogenesis, the formation of new blood vessels, plays key roles in organ regeneration. Newly formed vasculatures not only deliver oxygen, nutrients and various cell components that are required for organ regeneration but also provide instructive signals to the regenerating local tissues. Therefore, to successfully regenerate lungs in an adult, it is necessary to recapitulate the lung-specific microenvironments in which angiogenesis drives regeneration of local lung tissues. Although conventional in vivo angiogenesis assays, such as subcutaneous implantation of extracellular matrix (ECM)-rich hydrogels (e.g., fibrin or collagen gels or Matrigel – ECM protein mixture secreted by Engelbreth-Holm-Swarm mouse sarcoma cells), are extensively utilized to explore the general mechanisms of angiogenesis, lung-specific angiogenesis has not been well characterized because methods for orthotopic implantation of biomaterials in the lung have not been well established. The goal of this protocol is to introduce a unique method to implant fibrin gel on the lung surface of living adult mouse, allowing for the successful recapitulation of host lung-derived angiogenesis inside the gel. This approach enables researchers to explore the mechanisms by which the lung-specific microenvironment controls angiogenesis and alveolar regeneration in both normal and pathological conditions. Since implanted biomaterials release and supply physical and chemical signals to adjacent lung tissues, implantation of these biomaterials on diseased lung can potentially normalize the adjacent diseased tissues, enabling researchers to develop new therapeutic approaches for various types of lung diseases.
The overall goal of this protocol is to introduce a method to implant fibrin gel on the lung surface of adult mouse, which allows researchers to characterize the molecular mechanisms of lung vascular and alveolar development, and to leverage this knowledge in order to develop biomimetic materials capable of recapitulating physiological lung vascular and alveolar formation to treat various lung diseases.
More than 35 million Americans suffer from chronic lung diseases including chronic obstructive pulmonary disease and pulmonary fibrosis. These patients have long-lasting chronic respiratory symptoms such as shortness of breath, chest tightness, nagging cough, and tiredness, which significantly impair their daily life 1-3. Despite a great amount of effort to develop effective therapies for these lung diseases, currently there is no cure; therefore, quality of life for these patients is poor and economic and human costs are high 4-7. Currently, lung transplantation is the only way to save patients with end-stage chronic lung diseases. However, because of the shortage of transplant donors, high cost, serious complications, and low survival rate 8-11, transplantation is not an optimal approach. Recent rapid progress in tissue engineering techniques has enabled researchers to bioengineer implantable lung by repopulating decellularized whole lung with various types of progenitor cells or induced pluripotent stem (iPS) cells 12,13. However, these bioengineered lungs are functional in host animals only for several hours after implantation 12,14,15. Utilizing biomaterials to regenerate the complex structures and functions of lungs has also been fairly unsuccessful. This may be because key biological processes that govern adult lung regeneration have not been well explored. In the lung, formation of the vascular system is one of the earliest and most important events during development and regeneration 16-21. Newly formed vasculatures in the lung not only deliver oxygen, nutrients and various cell components required for organ formation, but also provide instructive regulatory signals to surrounding cells 22-25. Thus, angiogenesis plays key roles in regenerative alveolarization in adult lungs 24,26,27. In addition, deregulated angiogenesis contributes to chronic lung diseases such as chronic obstructive pulmonary disease (COPD) 28, bronchopulmonary dysplasia (BPD) 21-23, and pulmonary fibrosis 29. Thus, to develop more efficient strategies for engineering lungs or treating chronic lung diseases, it is necessary to understand the fundamental mechanisms of lung-specific angiogenesis.
Each organ displays unique mechanical and chemical properties, which may differ between physiological and pathological conditions 30-33. These organ-specific microenvironments regulate endothelial cell behaviors and orchestrate vascular network formation in an organ-specific manner 24,34-36. Thus, to develop more efficient strategies for lung regeneration, the mechanism underlying lung-specific angiogenesis needs to be understood. While conventional in vivo angiogenesis assays such as subcutaneous hydrogel implantation have been used extensively for angiogenesis research 37-39, those methods do not recapitulate organ-specific angiogenesis. Recently, a novel method to implant Matrigel in an elastic mold on the mouse lung has been developed and shown to successfully recruit blood vessels and lung epithelial cells into the gels 22. This unique approach will allow researchers to explore the mechanism of lung-specific angiogenesis as well as interactions between blood vessels and non-vascular lung cells in physiological and pathological conditions. Since 1) Matrigel is not suitable for clinical application; 2) the elastic mold used to cast the gel may affect interactions between hydrogels and host lung tissue and 3) the elastic mold on the lung potentially causes impairment of lung function and pain during respiration, as a more clinically relevant approach, a 3D fibrin matrix containing angiogenic factors (vascular endothelial growth factor (VEGF)/ basic fibroblast growth factor (bFGF)) has been implanted on the mouse lung without casting in the elastic mold, and has successfully recapitulated host lung-derived angiogenesis. Fibrin gel, polymer fibrils generated from thrombin-cleaved fibrinogen, is known to trap a variety of angiogenic factors such as bFGF and VEGF to accelerate angiogenesis in vivo 40,41. Because of its regenerative ability and biodegradable nature 42, fibrin gel is widely used in the field of tissue engineering.
This article introduces a novel and unique approach to implant fibrin gel on the lung surface of living adult mouse and demonstrates that host lung-derived angiogenesis is recapitulated inside the gels in vivo. This method, which enables researchers to study lung-specific angiogenesis, will likely lead to the development of new therapeutic approaches for various types of lung diseases and significantly advance efforts to successfully regenerate adult lung.
NOTE: The in vivo animal study was carried out in strict accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocol was reviewed and approved by the Animal Care and Use Committee of Boston Children’s Hospital (Protocol Numbers: 13-10-2526R,14-02-2568R). All drugs used in this protocol are pharmaceutical grade and these drugs are prepared under sterile conditions.
1. Fibrin Gel Preparation
2. Mouse Preparation
3. Mouse Surgery
4. Mouse Recovery
5. Harvesting the Lung
To examine whether host lung-derived vascular formation is recapitulated inside the biomaterials implanted on the lung, fibrin gels supplemented with major angiogenic factors VEGF and bFGF (0, 10 and 100 ng/ml each) were implanted on the surface of living mouse lungs as reported using Matrigel 22. Fibrin gels 47 that contain these angiogenic growth factors were fabricated as shown in Figure 1a. After thoracotomy, a small area of the left lung surface was scraped using forceps and the fabricated fibrin gel was implanted on the lung of the adult mouse using a small amount of fibrin glue, which is FDA approved and widely used as an effective sealant to stop air leaks and reduce bleeding in lung surgery 48,49 (Figure 1b). Most mice recovered without severe respiratory symptoms (e.g., pneumothorax, respiratory distress). Seven days after implantation, mice were euthanized and lungs were harvested. Implanted fibrin gel was incorporated into the host lung 7 days after implantation (Figure 1c). 3D reconstruction of confocal fluorescence images has shown that host-derived CD31-positive endothelial cells formed vascular networks inside the gels 7 days after implantation in a VEGF/bFGF dose-dependent way (Figure 2a, c). Type I (AQP5 positive) and type II (SP-B positive) lung epithelial cells were also recruited along newly formed blood vessels inside the gels that were supplemented with higher concentrations of VEGF and bFGF (each 100 ng/ml) (Figure 2a). H&E staining of histological sections revealed that other types of host cells also migrated into the gel 7 days after implantation (Figure 2b). These findings suggest that host lung-derived regenerative vascular networks are successfully constructed inside the fibrin gels that are supplemented with angiogenic factors and implanted on the surface of adult mouse lung.
Figure 1: (a) Fibrin gel prepared before implantation. (b) Fibrin gel implanted over the scraped visceral pleura of the left lung (arrowheads). (c) Implanted fibrin gel (arrowheads) incorporated into the host lung 7 days after implantation. Scale bars 1 mm.
Figure 2: (a) Fluorescence micrographs showing formation of vascular networks (CD31 positive; green) and recruited type I (AQP5-positive; magenta) or type II (SP-B positive; magenta) lung epithelial cells inside the fibrin gel supplemented with various concentrations of VEGF and bFGF (0, 10 and 100 ng/ml each) 7 days after implantation. Dashed lines indicate the interface between implanted fibrin gel and host lung. Scale bar: 20 µm. (b) Light micrograph of H&E staining showing infiltration of host cells into the fibrin gel 7 days after implantation. Arrows indicate the interface between the gel and host lung. Scale bar: 20 µm. (c) Graph showing projected areas of newly formed blood vessels in the fibrin gels that are supplemented with various concentrations of VEGF and bFGF (0, 10 and 100 ng/ml each) 7 days after implantation.
This article introduces a new method to implant biomaterials on the lung surface of living adult mouse. With this system, host lung-derived angiogenesis is successfully recapitulated inside the material. This system allows researchers to explore crosstalk between endothelial cells, other cells (e.g., epithelial cells, mesenchymal cells, immune cells) and various ECM components that are required for local angiogenesis 50-53 and alveolar regeneration 24,54. Although conventional in vivo subcutaneous hydrogel implantation has been used extensively for angiogenesis research 37-39, those methods do not recapitulate organ-specific angiogenesis. This system, in which hydrogel is implanted directly on the lung surface, will enable researchers to explore the roles of the lung-specific microenvironment in angiogenesis and alveolar regeneration in adult mouse lung. These gels can be fabricated from various ECM-rich biomaterials (e.g., collagens, fibrins) that can be supplemented with various chemical factors (e.g., angiogenic factors, growth factors) 55,56, progenitor cells and/or iPS cells. In addition to chemical factors, mechanical forces also control angiogenesis 23,37. The stiffness of fibrin gel changes in a fibrinogen concentration-dependent manner 57 and manipulating the fibrinogen concentration may affect angiogenesis not only through chemical signals but also through physical cues 58,59. Therefore, physicochemical properties of the fibrin gels may need to be optimized carefully to recapitulate physiological organ-specific angiogenesis in the future. Wound healing after scraping the visceral pleura also produces an endogenous fibrin clot, which includes various types of host cells and promotes the healing process and tissue regeneration. This natural clot may interact with the exogenously implanted fibrin gel, and hence control angiogenesis in the implanted gel. Fluorescently labeled fibrinogen may enable researchers to distinguish between natural fibrin clot and implanted fibrin gel and explore these mechanisms. Although this is a powerful method to characterize angiogenesis in adult mouse lungs, application to the study of lung development and diseases in neonatal mice would likely present technical challenges.
The ultimate goal of this study is to recruit functional blood vessels into fibrin gels implanted on diseased lungs and to use the matrix as a medical device to restore functional lung structures. Possible communications between host cells and the vascular and alveolar structures inside the gels as well as the functionality of these structures should be explored in future experiments. Since VEGF levels in the lungs are decreased in patients with BPD 60 and emphysema 61, adding VEGF to the matrix may improve recruitment of blood vessels into the matrix implanted on these diseased lungs. Mechanical properties also differ between healthy and diseased lungs 23,62. For example, expression of matrix metalloproteinases and lysyl oxidase, which control degradation and crosslinking of collagens, respectively, are altered in various lung diseases including COPD and pulmonary fibrosis 63-67. In diseased lungs, certain lineages of progenitors for lung endothelial and epithelial cells are depleted 68. Thus, manipulating these factors (angiogenic factors, ECMs, ECM stiffness) or implanting fibrin gels supplemented with progenitor cells 69 will likely lead to the formation of functional blood vessels inside the matrix and recovery of lung function in various pathological conditions. Since chemical factors can be supplemented inside the fibrin gels to modulate local angiogenesis, this system can also be utilized explore specific environmental cues that may normalize diseased lungs in chronic lung diseases.
In summary, this article introduces a method to implant fibrin hydrogel on the lung surface of living mouse, which enables researchers to characterize lung-specific angiogenesis in vivo. Modification of various factors (e.g., time course, concentrations and combinations of angiogenic factors, various kinds of hydrogels, physicochemical properties of hydrogels) in this system, will unveil the mechanisms of angiogenesis and regeneration in the lung. Thus, this system will significantly advance scientific knowledge of basic vascular biology, tissue engineering, as well as pulmonary medicine.
The authors have nothing to disclose.
This work was supported by funds from American Heart Association (A.M.), U.S. Department of Defense (BC074986), and Boston Children’s Hospital Faculty Career Development Fellowship (T.M., A.M.). The authors thank Amanda Jiang and Elisabeth Jiang for technical assistance.
Name of Material/ Equipment | Company | Catalog Number | Comments/Description |
Fibrinogen from human placenta | Sigma | F4883 | For fabrication of fibrin gel |
Thrombin from bovine plasma | Sigma | T9549 | For fabrication of fibrin gel |
Recombinant mouse VEGF 164 | R&D | 493-MV | For supplementation to fibrin gel |
Recombinant mouse bFGF | R&D | 3139-FB | For supplementation to fibrin gel |
Rodent Intubation Stand | Braintree Scientific INC | RIS 100 | For intubation |
Fiber-Optic Light Source | Fisher Scientific | 12-565-35 | For intubation |
20G Elastic catheter | B.Braun | 4251652-02 | For intubation |
MiniVent Ventilator | Harvard Apparatus | CGS-8009 | For ventilation |
Stemi DV4 Steromicroscope | Fisher Scientific | 12-070-515 | For surgey |
Absobable suture | Ethicon | PDP304 | Surgical suture |
Antibody against CD31 | BD Biosciences | 553370 | Immunohistochemistry |
Antibody against AQP5 | Abcam | AB78486 | Immunohistochemistry |
Antibody against SP-B | Millipore | AB40876 | Immunohistochemistry |