8. Remove the last washing DI-H2O from the bottle and incubate
trachea in 500 mL of 2% deoxycholate for 12 h at room
temperature, using an orbital shaker at 200 rpm.
9. Remove deoxycholate and wash trachea with DI-H2O for 6 h
at room temperature, using an orbital shaker at 200 rpm.
Changes DI-H2O every 2 h (see Note 3).
10. Sterilize the tracheal ECM-based bio-scaffold in a water solu-
tion containing 70% Ethanol and 2% antibiotic/antimycotic
solution for 30 min at room temperature, using an orbital
shaker at 200 rpm.
11. Extensively wash the ECM-based bio-scaffold with PBS sup-
plemented with 4% antibiotic/antimycotic solution at room
temperature using an orbital shaker at 200 rpm.
12. Before
chondrocyte
repopulation,
immerse
the
tracheal
ECM-based bio-scaffold in chondrocyte culture medium for
at least 1 h at room temperature.
3.3
Human
Chondrocyte
Propagation and
Maintenance
1. Maintain human chondrocyte cell line in 5% CO2 incubator at
37 C.
2. Monitor cells daily.
3. Once cell culture has reached 80% confluency, carefully aspirate
the culture medium from T75 flask (see Note 4).
4. Wash cells three times with 7 mL of PBS supplemented with 1%
antibiotic antimycotic solution.
5. Add 2 mL of trypsin-EDTA solution (see Note 5) and incubate
at 37 C until cell monolayer begins to detach from the bottom
of the tissue culture dish and cells dissociate (see Note 6).
6. Dilute cell suspension in 8 mL of chondrocyte culture medium
to neutralize trypsin action.
7. Dislodge cells by repeatedly and gently pipetting.
8. Collect cell suspension in a 15 mL centrifuge polystyrene tube
and centrifuge at 300 g for 5 min.
9. Remove supernatant and resuspended chondrocytes in 10 mL
of fresh culture medium.
10. Plate cells in a new culture dish and culture at 37 C in 5% CO2
incubator. Keep the passage ratio between 1:2 and 1:4,
depending on growth rate (see Note 7).
11. Change medium every 2–3 days.
12. Maintain cells in culture until they have reached 80% con-
fluency and passage them.
Reconstruction of a Bioprosthetic Trachea
163