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Method Article
Here we describe the model and approach to study functions of pulmonary alveolar macrophages in cancer metastasis. To demonstrate the role of these cells in metastasis, the syngeneic (4T1) model of breast cancer in conjunction with the depletion of alveolar macrophage with clodronate liposomes was used.
This paper describes the application of the syngeneic model of breast cancer (4T1) to the studies on a role of pulmonary alveolar macrophages in cancer metastasis. The 4T1 cells expressing GFP in combination with imaging and confocal microscopy are used to monitor tumor growth, track metastasizing tumor cells, and quantify the metastatic burden. These approaches are supplemented by digital histopathology that allows the automated and unbiased quantification of metastases. In this method the routinely prepared histological lung sections, which are stained with hematoxylin and eosin, are scanned and converted to the digital slides that are then analyzed by the self-trained pattern recognition software. In addition, we describe the flow cytometry approaches with the use of multiple cell surface markers to identify alveolar macrophages in the lungs. To determine impact of alveolar macrophages on metastases and antitumor immunity these cells are depleted with the clodronate-containing liposomes administrated intranasally to tumor-bearing mice. This approach leads to the specific and efficient depletion of this cell population as confirmed by flow cytometry. Tumor volumes and lung metastases are evaluated in mice depleted of alveolar macrophages, to determine the role of these cells in the metastatic progression of breast cancer.
The premetastatic niche is an important process in cancer metastasis defined as a set of alterations that occur in the organs that are targets for metastases prior to arrival of tumor cells1,2. Therefore, therapeutic targeting of this step of cancer progression may prevent metastases to the vital organs that cause approximately 90% of cancer-associated deaths. Although the concept of the premetastatic niche, also known as the "seed and soil" theory, was introduced more than a century ago, no experimental proof has been provided until recently, when the bone marrow-derived cells were demonstrated to contribute to the premetastatic soil1,3-7. Despite these developments, the premetastatic niche remains a largely understudied aspect of cancer pathophysiology and further research to identify cellular players and mechanisms involved is needed.
Here we report the in vivo approaches to study the role of alveolar macrophages in breast cancer metastases and the lung premetastatic niche. The alveolar macrophages arrive to the lungs early during the embryonic development and self-renew there during adulthood8. They also have important immunomodulatory and homeostatic functions including the protection of this organ from undesired inflammatory responses to the environmental innocuous antigens9. Therefore, we hypothesize that tumors exploit this physiological immunosuppression, imposed by alveolar macrophages, and, consequently, alveolar macrophages contribute to the lung premetastatic niche by suppressing antitumor immunity. This hypothesis is supported by our recent report demonstrating that the specific depletion of these cells reduces lung metastases and enhances antitumor T cell responses10.
For these studies we apply a well-established syngeneic model of breast cancer (4T1), which mimics stage IV metastatic breast cancer11; and has been previously reported in studies of the premetastatic niche6. To track metastasizing tumor cells in vivo we use 4T1 cells expressing GFP (4T1-GFP) in conjunction with animal imaging and confocal microscopy. We focus on the lung premetastatic niche, since this organ is one of the most common targets of hematogenous metastases of human malignancies12. To investigate functions of alveolar macrophages in the premetastatic niche, we use clodronate liposomes to deplete these cells13; and evaluate impact of this depletion on lung metastases. Of note, this method specifically depletes alveolar macrophages but no other phagocytic cells in the lungs or in circulation10.
Todos los estudios con animales han sido aprobados por Institucional Cuidado de Animales y el empleo Comisión de Texas Tech University Health Sciences Center y siguió las directrices que se describen en la "Guía para el Cuidado y Uso de Animales de Laboratorio", publicado por los Institutos Nacionales de Salud. Utilice ocho a doce semanas de edad ratones BALB / c hembra que están disponibles comercialmente. Inyectar 1 x 10 5 4T1 o 1 x 10 5 4T1 células que expresan GFP, que se puede adquirir de varios fabricantes, en la almohadilla de grasa mamaria.
1. Cultura de 4T1 y 4T1-GFP Células y Preparación de tumor de células de suspensión para inyección 14
2. Administración intranasal de liposomas 10
NOTA: Realizar todos los pasos que utilizan soluciones estériles en un flujo de aire laminar (LAF) Gabinete de Bioseguridad menos que se especifique lo contrario.
3. Sacrificio Mouse y Recogida de tejido
NOTA: El uso en autoclave e instrumentos estériles para la disección del ratón. La eutanasia a los ratones, mientras que bajo anestesia a través de la exanguinación y la eliminación de los órganos vitales.
4. Evaluación de pulmón metástasis
5. citometría de flujo (FACS) Análisis de los macrófagos alveolares en los Pulmones
6. Análisis de los datos de FACS: Estrategias de apertura de puerta y la determinación de las subpoblaciones de células
La inyección de las células tumorales 4T1-GFP en la almohadilla de grasa mamaria conduce a la formación de tumores de ratón (figura 1A) que recapitular la propagación metastásica del cáncer de mama humano, como metástasis se forman rápidamente en los pulmones (Figura 2), hígado, huesos y el cerebro de los ratones 11. La transfección estable de células 4T1 con GFP facilita el seguimiento del crecimiento del tumor (Figura 1B)...
The recent insights into cancer biology and causative factors involved in carcinogenesis and tumor progression lead to development of genetically engineered mouse (GEM) models of cancer, in which tumors grow spontaneously, usually over a period of several months15. Although these tumor models appear to reflect better the natural history of human malignancies than xenografts or syngeneic models, much time required for tumor development and various degrees of malignant phenotype penetrance limit the use of these...
Los autores declaran que no tienen intereses financieros en competencia.
Esta investigación ha sido financiada por el Departamento de Defensa conceder TSA 140010 a 111038 y BC MK de MMM Puntos de vista y opiniones de los endosos, y por el autor (s) no reflejan las del Ejército de Estados Unidos o el Departamento de Defensa.
Name | Company | Catalog Number | Comments |
4T1 cell line | American Type Culture Collection, Manassas, VA, USA | CRL 2539 | Tumor cells |
4T1-GFP cell line | Caliper life sciences/ Perkin Elmer, Waltham, MA, USA | BW128090 | Tumor cells |
RPMI | Corning, Corning, NY, USA | 10-040-CM | Media |
Heat inactivated FBS | Gibco (Thermo Scientific), USA | 10082147 | Media |
Penicillin Streptomycin | Fisher Scientific, Waltham, MA, USA | MT-300-02-CI | Media |
PBS | Fisher Scientific, Waltham, MA, USA | BP399-20 | Dilute with distilled water |
Trypsin 0.25% with EDTA | Hyclone, Logan, Utah, USA | SH30042.02 | Tissue culture supplies |
T75 cm2 flask | Fisher Scientific, Waltham, MA, USA | 12-565-32 | Tissue culture supplies |
15 ml conical tube | BD falcon, Franklin Lakes, NJ, USA | 352096 | Tissue culture supplies |
50 ml conical tube | BD falcon, Franklin Lakes, NJ, USA | 352098 | Tissue culture supplies |
60 mm2 Petri dish | Fisher Scientific, Waltham, MA, USA | AS4052 | For lung imaging |
Isoflurane (Isothesia) | Butler Schein Animal health, Dublin, OH, USA | NDC 11695-6776-2 | Mouse anesthesia |
Clodronate liposomes | Formumax Scientific Inc, Palo Alto, CA, USA | F70101C-N | Macrophages depletion |
Control liposomes | Formumax Scientific Inc, Palo Alto, CA, USA | F70101-N | Control PBS-liposomes |
29 gauge insulin syringes (12.7 mm and 0.5 ml capacity)- Reli-On | Walmart, Bentonville, AR, USA | For tumor cell injection | |
Hair removal cream (Nair) | Walmart, Bentonville, AR, USA | ||
Paraformaldehyde solution (4%) | Affymetrix, Santa Clara, CA, USA | 19943-I Lt | Dilute to 4% or 1% using 1x PBS |
OCT compound | Fisher Scientific, Waltham, MA, USA | 230-730-571 | For freezing tissue in cryomolds |
Fluoro-Gel-II with DAPI | Electron Microscopy Sciences, Hatfield, PA, USA | 17985-51 | Mounting medium |
Sucrose | Sigma, St. Louis, MO, USA | S-9378 | Cryopreservation |
Collagenase P | Roche, Basel, Switzerland | 11249002001 | Components of tissue digestion buffer |
Dnase I | Roche, Basel, Switzerland | 10104159001 | Components of tissue digestion buffer |
Trypsin inhibitor | Sigma, St. Louis, MO, USA | T9253 | Components of tissue digestion buffer |
40 micron cell strainers | Fisher Scientific, Waltham, MA, USA | 22-363-547 | Used in tissue digestion to remove clumps |
Trustain FcX-Fc Block (CD16/CD32) | Biolegend, San Diego, CA, USA | 101320 | Antibodies for flow cytometry |
BV605 CD45 | Biolegend, San Diego, CA, USA | 103139 | Antibodies for flow cytometry |
PE CD11b | Biolegend, San Diego, CA, USA | 101207 | Antibodies for flow cytometry |
PE Cy7 F4/80 | Biolegend, San Diego, CA, USA | 123113 | Antibodies for flow cytometry |
APC/Cy7 CD11c | Biolegend, San Diego, CA, USA | 117323 | Antibodies for flow cytometry |
PerCPcy5.5 IA/IE (MHCII) | Biolegend, San Diego, CA, USA | 107625 | Antibodies for flow cytometry |
PE CD80 | Biolegend, San Diego, CA, USA | 104707 | Antibodies for flow cytometry |
AF647 CD86 | Biolegend, San Diego, CA, USA | 105019 | Antibodies for flow cytometry |
Fixable viability Dye eflour 506 | eBioscience, San Diego, CA,USA | 65-0866 | Antibodies for flow cytometry |
Cryostat | Leica Biosystems, Buffalo Grove, IL, USA | CM1850 | Cryosectioning |
UVP iBox Explorer | UVP Inc, Upland, CA, USA | Mouse and lung fluorescent imaging | |
Aperio Scanscope CS | Leica Biosystems, Buffalo Grove, IL, USA | Digital pathology | |
BD LSRFortessa | BD Biosciences, Franklin Lakes, NJ, USA | Flow cytometry/data acquisition | |
Nikon A1 confocal TE2000 microscope | Nikon Instruments Inc., Melville, NY 11747-3064, U.S.A. | Imaging and quantifying GFP fluorescence in lung cryosections | |
UVP visionworks software (Version 7.1RC3.38) | UVP Inc, Upland, CA, USA | Imaging software for iBOX | |
Aperio Imagescope software (v12.1.0.5029) | Leica Biosystems, Buffalo Grove, IL, USA | Imaging software for analysis of digital slides | |
Flow JO software (version 9.8.1) | Flow JO LLC, Ashland, OR, USA | Analysis of flow cytometric data | |
NIS Elements AR (version 4.20.01) 64 Bit | Nikon Instruments Inc., Melville, NY 11747-3064, U.S.A. | Acquisition and analysis of lung cryosections for GFP |
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