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Dans cet article

  • Overview
  • Protocole
  • Déclarations de divulgation
  • matériels

Overview

This video describes a method of generating an organ conditioned medium derived from the mouse liver. This model system can be used to identify and study organ-derived soluble factors and their effects on the organ tropism and metastatic behavior of cancer cells.

Protocole

1. Generation of Lung- and Brain- Conditioned Media

  1. In a sterile tissue culture hood, invert PBS tubes containing lung or brain three times to remove residual blood from organs and aspirate PBS containing blood. Repeat with fresh cold PBS until solution appears clear with no evidence of blood.
  2. Place lungs and brains in separate 60 mm2 glass petri dishes. Using two sterile scalpel blades, mince lungs or brains by repeatedly slicing back and forth until tissue fragments are approximately ~ 1 mm3 in size.
  3. Determine the amount of media needed to resuspend tissue fragments from the calculated weight difference.
    NOTE: Lung and brain tissue are weight normalized by resuspension in a 4:1 media:tissue ratio (vol/wt).
  4. Resuspend tissue fragments in appropriate volume (determined previously in step 1.3) of Dulbecco's Modified Eagle's Medium (DMEM):F12 media supplemented with 1x concentrated mitogen supplement and penicillin (50 µg/ml)/streptomycin (50 µg/ml).
  5. Add resuspended lung or brain tissue fragments to one well of a 6-well plate.
  6. Incubate tissue fragments in media for 24 hr at 37 °C and 5% CO2. Following incubation, collect conditioned media for each tissue and further dilute by adding three equivalent volumes of fresh media in a 50 ml conical tube.
  7. Centrifuge at 1,000 x g in diluted conditioned media for each organ at 4 °C for 15 min to remove large tissue debris. Collect media supernatant and filter through a 0.22 µm syringe filter.
  8. Pool conditioned media from each organ (i.e., lung with lung and brain with brain) from multiple mice to account for mouse-to-mouse variability. Aliquot and store conditioned media at -80 °C until use.

Déclarations de divulgation

No conflicts of interest declared.

matériels

NameCompanyCatalog NumberComments
1x Phosphate-buffered salineThermoFisher Scientific10010-023Keep sterile
60 mm2 glass petri dishesSigma-AldrichCLS7016560Keep sterile
DMEM:F12Life Technologies21331-020Warm in 37 °C water bath before use, keep sterile
Penicillin-Streptomycin (10,000 U/ ml)Life Technologies15140-122Keep sterile
50 ml conical tubesThermo Scientific (Nunc)339652Keep sterile
0.22 μm syringe filtersSigma-AldrichZ359904Keep sterile
6-well tissue culture platesThermo Scientific (Nunc)140675Keep sterile
Scalpel bladesFisher ScientificS95937AKeep sterile

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