An Assay to Study the Regulation of Macrophage Phagocytosis by Mesenchymal Stem Cells
내레이션 대본
Gently aspirate the medium from the experimental wells containing mesenchymal stem cells. Use a multichannel micro-pipette to add 100 microliters of the treated and the control macrophage cell suspensions in the appropriate experimental wells according to the plate design, and incubate overnight as demonstrated. Add one milliliter of live-cell imaging medium to the vial containing one milligram of zymosan particles, and collect the medium particle mixture into a glass culture tube.
After rinsing the vial with an additional one milliliter of imaging solution, transfer the rinsed imaging medium in the glass tube. Then, add 3 milliliters of additional imaging solution to achieve 0.2 mg/ml zymosan particle suspension. Vortex the zymosan suspension using quick pulses for 30 to 60 seconds. Then, use a probe sonicator to sonicate the suspension with 60 quick pulses. After aspirating the medium, rinse the experimental wells in reagent blank wells with 100 microliters of live-cell imaging solution.
Next, aspirate the live-cell imaging solution from the wells, and add 100 microliters of the zymosan suspension. Open the plate tray of the fluorescent reader using the touch-pad interface. Set the plate without the lid in the tray with the A1 well, in the upper left corner. Close the tray using the touch-pad, and click on the green "Read" button in the top menu.
