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Nanoplastics causes extensive congenital malformations during embryonic development by passively targeting neural crest cells
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Researchers exposed chicken embryos to polystyrene nanoplastics and found far more severe birth defects than previously reported, including major heart malformations. They discovered that nanoplastics selectively bind to neural crest cells, which are critical for the development of many organs, causing these cells to die or fail to migrate properly. The findings raise concerns that the growing burden of nanoplastics in the environment may pose risks to embryonic development.
Nanomaterials are widespread in the human environment as pollutants, and are being actively developed for use in human medicine. We have investigated how the size and dose of polystyrene nanoparticles affects malformations in chicken embryos, and have characterized the mechanisms by which they interfere with normal development. We find that nanoplastics can cross the embryonic gut wall. When injected into the vitelline vein, nanoplastics become distributed in the circulation to multiple organs. We find that the exposure of embryos to polystyrene nanoparticles produces malformations that are far more serious and extensive than has been previously reported. These malformations include major congenital heart defects that impair cardiac function. We show that the mechanism of toxicity is the selective binding of polystyrene nanoplastics nanoparticles to neural crest cells, leading to the death and impaired migration of those cells. Consistent with our new model, most of the malformations seen in this study are in organs that depend for their normal development on neural crest cells. These results are a matter of concern given the large and growing burden of nanoplastics in the environment. Our findings suggest that nanoplastics may pose a health risk to the developing embryo.
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Researchers found that polystyrene nanoplastics caused defective neural tube development in embryos through disruption of normal cell death processes and caveolae-mediated cellular uptake. The study suggests that nanoplastics, which can cross the placental barrier, may pose risks to fetal development by interfering with critical early-stage neurological formation.
Polystyrene nanoplastics exposure caused defective neural tube morphogenesis through caveolae-mediated endocytosis and faulty apoptosis
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This study found that polystyrene nanoplastics caused abnormal neural tube formation in early embryonic development by being taken up through a specific cellular pathway and triggering defective cell death. The findings suggest nanoplastics could potentially interfere with fetal brain development, raising serious concerns about exposure during pregnancy.
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Researchers found that polystyrene nanoplastics disrupted the development of heart cells grown from human embryonic stem cells, producing smaller and weaker heart tissue in the lab. The nanoplastics caused oxidative stress in mitochondria and blocked important cellular cleanup processes, reducing the stem cells' ability to properly form heart cells. In zebrafish embryos, nanoplastic exposure also reduced heart contractions and blood flow, suggesting that nanoplastic exposure during pregnancy could pose risks to fetal heart development.
Can exposure to micro- and nanoplastics disrupt neural crest development? Evidence and a testable model for MNP-associated environmental neurocristopathies
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This review paper summarizes existing research on whether micro- and nanoplastics could affect "neural crest cells," special embryonic cells that form facial, heart, and nerve structures. It discusses evidence from chick embryo studies showing links between plastic particles and cell abnormalities, but states this remains an unproven framework, not an established cause-and-effect relationship in humans.
The biodistribution of polystyrene nanoparticles administered intravenously in the chicken embryo
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Researchers injected polystyrene nanoplastics into chicken embryos and tracked where the particles traveled, finding high accumulations in the heart, liver, and kidneys, with particles crossing critical tissue barriers. This is an important advance in understanding how nanoplastics distribute throughout a developing organism, with potential implications for fetal health.
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