Method for preparing a cell-derived extracellular matrix membrane
A cell and decellularization technology, applied in biochemical equipment and methods, animal cells, vertebrate cells, etc., can solve the problems of difficult tissue collection, uncontrolled biodegradation of amniotic membrane, low biocompatibility, etc.
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[0034] One object of the present invention relates to a method for preparing an ECM membrane for tissue engineering through high-density culture and an ECM membrane prepared by the same method. In particular, the present invention relates to a method for preparing a chondrocyte-derived ECM membrane, the method comprising the following steps: (a) isolating chondrocytes from animal-derived cartilage, and then culturing them; (b) obtaining Chondrocyte / ECM membrane; and (c) ECM membrane obtained by removing cells from the chondrocyte / ECM membrane, and drying the resulting membrane, and ECM membrane prepared by the same method.
[0035] In the present invention, the above method may include an additional step (d): re-culturing to obtain a thick ECM membrane with high compressive force by replanting chondrocytes on the obtained ECM membrane.
[0036]In one embodiment of the present invention, by controlling the thickness of chondrocytes, chondrocytes are used to prepare ECM membrane...
Embodiment 1
[0060] Example 1: Isolation of porcine chondrocytes
[0061] 2-week-old pigs that were not infected with cholera, other viruses, or infectious diseases were sacrificed by excessive paralysis in accordance with animal care laws. In a sterile environment, remove the cartilage from the posterior knee joint. The removed cartilage was then cut into small pieces on a clean work surface and treated with 0.1% collagenase for 12 hours. After filtering the cells through a 0.4 μm filter, the chondrocytes were isolated by centrifugation.
Embodiment 2
[0062] Example 2: Preparation of chondrocyte-derived ECM membranes
[0063] The chondrocytes isolated in Example 1 were separated at 0.7 × 10 5 The cells were planted on 6-well culture dishes at a concentration of per square centimeter, and cultured in medium (DMEM+20% FBS+1% penicillin-streptomycin+5 μg / mL ascorbic acid) for 3 weeks. The medium was changed every three days. After 3 weeks, the ECM film was washed three times with PBS and detached from the 6-well dish. The prepared ECM film presents a translucent film type ( figure 1 ).
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