Fluorescence Based Transwell Macrophage Attraction Assay: An In Vitro Method to Study Tumor-Macrophage Interaction Through Chemical-Induced Chemotaxis
Transcript
In response to certain chemical attractants released by solid tumors, immune cells such as tumor-associated macrophages or TAMs infiltrate the solid tumors. Subsequently, these TAMs facilitate tumor progression.
To study the interactions between TAMs and tumor cells in vitro, begin by taking a multiwell plate with a membranous insert. This arrangement temporarily separates the well into two compartments.
Next, add a suspension of TAMs to the upper compartment of the transwell.
Supplement the lower compartment of the transwell with a conditioned medium enriched with chemical attractants secreted by tumor cells.
Incubate the plate for the desired time.
During incubation, chemical modulators attract TAMs. This leads to the movement of TAMs into the lower compartment via the porous insert membrane through chemical-induced chemotaxis.
Now, remove the insert from the well. Transfer the conditioned medium containing the migrant TAM population into a suitable plate for fluorescent measurement.
Treat the cells with a lysis buffer containing fluorescent dye. This buffer lyses the macrophages. Eventually, the dye molecules bind to the nucleic acids, producing an enhanced fluorescence.
Finally, scan the plate using a fluorescence plate reader. A high fluorescence indicates the successful migration of macrophages through chemical-induced chemotaxis.
