4.7 Article

Effects of Titanium Dioxide Nanoparticles on Cell Growth and Migration of A549 Cells under Simulated Microgravity

期刊

NANOMATERIALS
卷 12, 期 11, 页码 -

出版社

MDPI
DOI: 10.3390/nano12111879

关键词

simulated microgravity; titanium dioxide nanoparticles; cell migration; cytoskeleton; focal adhesion kinase

资金

  1. National Key Research and Development Program of China [2020YFA0710700]
  2. Directional Institutionalized Scientific Research Platform relies on Beijing Synchrotron Radiation Facility of Chinese Academy of Sciences

向作者/读者索取更多资源

With the increasing application of nanomaterials in aerospace technology, the health concerns of astronauts regarding long-term space exposure to nanomaterials under radiation and microgravity conditions have been raised. This study simulated microgravity using a random positioning machine (RPM) and investigated the behaviors of cells under simulated microgravity as well as the potential toxicity of titanium dioxide nanoparticles (TiO2 NPs). The results showed that simulated microgravity had no significant effect on cell viability, but it could reduce cell migration. The exposure to TiO2 NPs inhibited cell migration under both gravity conditions, but to a milder extent under simulated microgravity.
With the increasing application of nanomaterials in aerospace technology, the long-term space exposure to nanomaterials especially in the space full of radiation coupled with microgravity condition has aroused great health concerns of the astronauts. However, few studies have been conducted to assess these effects, which are crucial for seeking the possible intervention strategy. Herein, using a random positioning machine (RPM) to simulate microgravity, we investigated the behaviors of cells under simulated microgravity and also evaluated the possible toxicity of titanium dioxide nanoparticles (TiO2 NPs), a multifunctional nanomaterial with potential application in aerospace. Pulmonary epithelial cells A549 were exposed to normal gravity (1 g) and simulated gravity (similar to 10(-3) g), respectively. The results showed that simulated microgravity had no significant effect on the viability of A549 cells as compared with normal gravity within 48 h. The effects of TiO2 NPs exposure on cell viability and apoptosis were marginal with only a slightly decrease in cell viability and a subtle increase in apoptosis rate observed at a high concentration of TiO2 NPs (100 mu g/mL). However, it was observed that the exposure to simulated microgravity could obviously reduce A549 cell migration compared with normal gravity. The disruption of F-actin network and the deactivation of FAK (Tyr397) might be responsible for the impaired mobility of simulated microgravity-exposed A549 cells. TiO2 NPs exposure inhibited cell migration under two different gravity conditions, but to different degrees, with a milder inhibition under simulated microgravity. Meanwhile, it was found that A549 cells internalized more TiO2 NPs under normal gravity than simulated microgravity, which may account for the lower cytotoxicity and the lighter inhibition of cell migration induced by the same exposure concentration of TiO2 NPs under simulated microgravity at least partially. Our study has provided some tentative information on the effects of TiO2 NPs exposure on cell behaviors under simulated microgravity.

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