The FasL hijacks a normal transport pathway for melanin, the pigment that melanosomes load into microvesicles and send to neighboring keratinocytes. In melanoma cells, these microvesicles, or exosomes, are also loaded with FasL, which can trigger apoptosis in Fas-expressing immune cells that might otherwise counteract tumor growth.
This mechanism of counterattack may operate in other tumors, as microvesicles are released from a number of cell types. In the case of melanoma cells, the new work clears up a controversy. Microvesicles explain how melanoma cells can have an apoptotic effect (the initial observation) without expressing FasL on their cell surface...
The Rockefeller University Press
2002
The Rockefeller University Press
2002
You do not currently have access to this content.