Skip to main content
. 2016 Apr 29;7:645–654. doi: 10.3762/bjnano.7.57

Table 2.

Main mechanisms of neurotoxicity of titanium dioxide nanoparticles in in vitro studies.

cell types mechanisms of neurotoxicity references

BV2 OS (ROS, H2O2 elevated) [1920]
primary hippocampal neurons multiple mechanisms (disrupted glutamate metabolism and dysregulated levels of NMDARs) [56]
primary hippocampal neurons apoptosis mediated by mitochondria- and endoplasmic reticulum-pathways [35]
primary astrocytes direct impairment of mitochondria and ROS [38]
D384 and SH-SY5Y direct impairment of mitochondria and cell membrane [39]
SH-SY5Y direct impairment of microtubules and cell morphology [40]
SH-SY5Y multiple mechanisms (changed cell cycle, apoptosis, and DNA damage) [53]
C6 and U373 OS and impairment of mitochondria [48]
C6 and U373 multiple mechanisms (inhibited cell proliferation, morphological change and apoptosis) [52]
N9 apoptosis [36]
U87 apoptosis [37]
PC12 multiple mechanisms (OS and apoptosis) [51]
PC12 other mechanisms (signaling pathway activated and arrested cell cycle) [63]