Endocytosis
is a cellular process in which substances are engulfed
by the cellular membrane and budded off inside the cells to form vesicles.
It plays key roles in controlling nutritional component uptake, immune
responses, and other biological functions. A comprehensive understanding
of endocytosis gives insights into such physiological functions and
informs the design of medical nanodevices that need to enter cells.
So far, endocytosis has been studied mostly using established cell
lines. However, the established cell lines generally originate from
cancer cells or are transformed from normal cells into immortalized
cells. Therefore, primary cells may give us more reliable information
about the endocytosis process of nanoparticles into cells. In this
research, we studied the uptake of gold nanorods (AuNRs) with four
different surface modifications (anionic/cationic polymers and anionic/cationic
silica) by two kinds of primary cells (human monocyte-derived macrophages
and human umbilical vein endothelial cells) and two kinds of established
cell lines (HeLa cells and RAW 264.7 cells). We found that the surface
properties of AuNRs affected their cellular uptake, and the cationic
surface tended was advantageous for uptake, but it depended on the
cell types. Control experiments using inhibitors of representative
endocytosis pathways (macropinocytosis, clathrin-mediated endocytosis,
and caveolae-mediated endocytosis) indicated that primary cells had
a dominant uptake pathway for internalization of the AuNRs, whereas
the established cell lines had multiple pathways. Our results provide
us with novel insights into cellular uptake of AuNRs in that they
depend not only on surface characters of the nanoparticles but also
cell types, such as primary cells and established cell lines.