Abstract
Nanoparticles (NPs) are considered safe for prolonged internalization in cells.
During the latest years, an increasing amount of studies indicates cytotoxic effects of different nanoparticles (NPs). On the subject of genotoxicity, carcinogenicity and stem-cell-related toxicity, conflicting results are reported. Stem cells are an important target in several applications of NPs, f.e. in stem cell tracking systems, regenerative medicine and anti-cancer drugs... New insights in the toxicity of nanoparticles on stem cells not only address these aspects, they also contribute to our knowledge on defense mechanisms of different tissues. It is generally known that the intrinsic cellular repair capacity varies with the degree of cell potency, an important matter in developmental toxicity as well as in species- or tissue-related plasticity. Schmidtea mediterranea is a small invertebrate with an easy accessible population of totipotent stem cells. This makes it possible to study underlying mechanisms of nanoparticle toxicity on stem cells in vivo, and as such link them to physiological parameters. We focus on the toxicity and biocompatibility of silver NPs (AgNPs) and silica NPs (SiNPs) on stem-cell-specific activities. Both AgNPs and SiNPs are extensively used in biomedical applications, s.a. disinfectants, implants, as drug carriers or in bio-imaging. In our in vivo model system, we observed the uptake of AgNPs in stem cells via transmission electron microscopy. Stem cells responded by a proliferation decrease, measured via histon H3 immunostaining. We are currently looking into the underlying cause of this decrease, as the genotoxic character of this element is still under debate. Effects on cell cycle progression and differentiation were investigated by looking into the expression of the smedwi-1 gene and corresponding protein levels, both exclusively present in stem cells and indicative for different phases of the cell cycle. At the phenotypic level, concentration-dependent behavioral effects, including looper movements and curling, were observed. Exposure to a range of SiNPs concentrations showed no clear phenotypic or proliferation effects. This is a promising result for the further use of SiNPs, but extra research on the uptake and the effects of coating, and the influence of external parameters are needed for both NP types to confirm initial results.
During the latest years, an increasing amount of studies indicates cytotoxic effects of different nanoparticles (NPs). On the subject of genotoxicity, carcinogenicity and stem-cell-related toxicity, conflicting results are reported. Stem cells are an important target in several applications of NPs, f.e. in stem cell tracking systems, regenerative medicine and anti-cancer drugs... New insights in the toxicity of nanoparticles on stem cells not only address these aspects, they also contribute to our knowledge on defense mechanisms of different tissues. It is generally known that the intrinsic cellular repair capacity varies with the degree of cell potency, an important matter in developmental toxicity as well as in species- or tissue-related plasticity. Schmidtea mediterranea is a small invertebrate with an easy accessible population of totipotent stem cells. This makes it possible to study underlying mechanisms of nanoparticle toxicity on stem cells in vivo, and as such link them to physiological parameters. We focus on the toxicity and biocompatibility of silver NPs (AgNPs) and silica NPs (SiNPs) on stem-cell-specific activities. Both AgNPs and SiNPs are extensively used in biomedical applications, s.a. disinfectants, implants, as drug carriers or in bio-imaging. In our in vivo model system, we observed the uptake of AgNPs in stem cells via transmission electron microscopy. Stem cells responded by a proliferation decrease, measured via histon H3 immunostaining. We are currently looking into the underlying cause of this decrease, as the genotoxic character of this element is still under debate. Effects on cell cycle progression and differentiation were investigated by looking into the expression of the smedwi-1 gene and corresponding protein levels, both exclusively present in stem cells and indicative for different phases of the cell cycle. At the phenotypic level, concentration-dependent behavioral effects, including looper movements and curling, were observed. Exposure to a range of SiNPs concentrations showed no clear phenotypic or proliferation effects. This is a promising result for the further use of SiNPs, but extra research on the uptake and the effects of coating, and the influence of external parameters are needed for both NP types to confirm initial results.
Original language | English |
---|---|
Pages | 179 |
Publication status | Published - May 2017 |
Event | Society of Environmental Toxicology and Chemistry (SETAC) - Europe 27th Annual Meeting: SETAC 2017 - Square - Brussels Meeting Centre, Brussel, Belgium Duration: 7 May 2017 → 11 May 2017 https://www.setac.org/page/AnnualMeetings |
Conference
Conference | Society of Environmental Toxicology and Chemistry (SETAC) - Europe 27th Annual Meeting |
---|---|
Country/Territory | Belgium |
City | Brussel |
Period | 7/05/17 → 11/05/17 |
Internet address |