TY - JOUR
T1 - Targeting of nanoparticles to the clathrin-mediated endocytic pathway
AU - Harush-Frenkel, Oshrat
AU - Debotton, Nir
AU - Benita, Simon
AU - Altschuler, Yoram
PY - 2007/2/2
Y1 - 2007/2/2
N2 - Nanoparticles (NPs) are considered attractive carriers for gene therapy and drug delivery owing to their minor toxic effect and their ability to associate and internalize into mammalian cells. In this study, we compared the endocytosis into HeLa cells of NPs exposing either a negative or positive charge on their surface. The exposed charge significantly affected their ability to internalize as well as the cellular endocytosis mechanism utilized. Negatively charged NPs show an inferior rate of endocytosis and do not utilize the clathrin-mediated endocytosis pathway. On the other hand, positively charged NPs internalize rapidly via the clathrin-mediated pathway. When this pathway is blocked, NPs activate a compensatory endocytosis pathway that results in even higher accumulation of NPs. Overall, the addition of a positive charge to NPs may improve their potential as nanoparticulate carriers for drug delivery.
AB - Nanoparticles (NPs) are considered attractive carriers for gene therapy and drug delivery owing to their minor toxic effect and their ability to associate and internalize into mammalian cells. In this study, we compared the endocytosis into HeLa cells of NPs exposing either a negative or positive charge on their surface. The exposed charge significantly affected their ability to internalize as well as the cellular endocytosis mechanism utilized. Negatively charged NPs show an inferior rate of endocytosis and do not utilize the clathrin-mediated endocytosis pathway. On the other hand, positively charged NPs internalize rapidly via the clathrin-mediated pathway. When this pathway is blocked, NPs activate a compensatory endocytosis pathway that results in even higher accumulation of NPs. Overall, the addition of a positive charge to NPs may improve their potential as nanoparticulate carriers for drug delivery.
KW - Clathrin
KW - Endocytosis
KW - HeLa cells
KW - Macropinocytosis
KW - Nanoparticles
UR - http://www.scopus.com/inward/record.url?scp=33845658279&partnerID=8YFLogxK
U2 - 10.1016/j.bbrc.2006.11.135
DO - 10.1016/j.bbrc.2006.11.135
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C2 - 17184736
AN - SCOPUS:33845658279
SN - 0006-291X
VL - 353
SP - 26
EP - 32
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 1
ER -