TY - JOUR
T1 - Cell-cell communication between malaria-infected red blood cells via exosome-like vesicles
AU - Regev-Rudzki, Neta
AU - Wilson, Danny W
AU - Carvalho, Teresa G
AU - Sisquella, Xavier
AU - Coleman, Bradley M
AU - Rug, Melanie
AU - Bursac, Dejan
AU - Angrisano, Fiona
AU - Gee, Michelle
AU - Hill, Andrew Francis
AU - Baum, Jake
AU - Cowman, Alan Frederick
PY - 2013
Y1 - 2013
N2 - Cell-cell communication is an important mechanism for information exchange promoting cell survival for the control of features such as population density and differentiation. We determined that Plasmodium falciparum-infected red blood cells directly communicate between parasites within a population using exosome-like vesicles that are capable of delivering genes. Importantly, communication via exosome-like vesicles promotes differentiation to sexual forms at a rate that suggests that signaling is involved. Furthermore, we have identified a P. falciparum protein, PfPTP2, that plays a key role in efficient communication. This study reveals a previously unidentified pathway of P. falciparum biology critical for survival in the host and transmission to mosquitoes. This identifies a pathway for the development of agents to block parasite transmission from the human host to the mosquito.
AB - Cell-cell communication is an important mechanism for information exchange promoting cell survival for the control of features such as population density and differentiation. We determined that Plasmodium falciparum-infected red blood cells directly communicate between parasites within a population using exosome-like vesicles that are capable of delivering genes. Importantly, communication via exosome-like vesicles promotes differentiation to sexual forms at a rate that suggests that signaling is involved. Furthermore, we have identified a P. falciparum protein, PfPTP2, that plays a key role in efficient communication. This study reveals a previously unidentified pathway of P. falciparum biology critical for survival in the host and transmission to mosquitoes. This identifies a pathway for the development of agents to block parasite transmission from the human host to the mosquito.
UR - http://www.sciencedirect.com/science/article/pii/S0092867413005047
U2 - 10.1016/j.cell.2013.04.029
DO - 10.1016/j.cell.2013.04.029
M3 - Article
SN - 0092-8674
VL - 153
SP - 1120
EP - 1133
JO - Cell
JF - Cell
IS - 5
ER -