Robert A Mans, Hannah Kelehear, Sarah Rotschafer, Clare Ganas, Brendan Uche-Moon, Gabrielle Call, Callie C Mauersberg, Justin Toller, Andrew Diamanduros
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引用次数: 0
Abstract
Microscopic plastic particles (micro- and nanoplastics) are an emerging environmental contaminant detected in air, soil, water, and human food supplies. Experiments using zebrafish have shown that polystyrene nanoplastics will infiltrate numerous organ systems after ingestion, including the brain, liver, muscle, and reproductive organs. Additionally, work in rodent models and cell culture has demonstrated that nanoplastics can induce inflammatory responses by microglia and alter astrocyte function. However, the responses of microglia and astrocytes in the zebrafish brain caused by daily exposures to nanoplastics have not been tested previously. In the current study, adult zebrafish were exposed to a nanoplastic-enriched diet consisting of Artemia brine shrimp containing 44 nm polystyrene spheres, and reactive gliosis by microglia and astrocytes was examined. Microglial 4C4-immunoreactive protein was elevated in the brains of zebrafish exposed to the nanoplastic-enriched diet. Levels of glial fibrillary acidic protein (GFAP) were not affected by plastic exposure. It was determined that microglial, but not astrocytic, markers were elevated in the zebrafish brain after 14-days of exposure to a nanopolystyrene-enriched diet. These findings contribute to our understanding of how a pervasive environmental contaminant, nanoplastics, may impair brain health, especially during the initial stages of nanoplastic exposure. Additionally, this is the first study using zebrafish to evaluate glial activation in the context of nanoplastic-contaminated foods.
期刊介绍:
Frontiers in Molecular Neuroscience is a first-tier electronic journal devoted to identifying key molecules, as well as their functions and interactions, that underlie the structure, design and function of the brain across all levels. The scope of our journal encompasses synaptic and cellular proteins, coding and non-coding RNA, and molecular mechanisms regulating cellular and dendritic RNA translation. In recent years, a plethora of new cellular and synaptic players have been identified from reduced systems, such as neuronal cultures, but the relevance of these molecules in terms of cellular and synaptic function and plasticity in the living brain and its circuits has not been validated. The effects of spine growth and density observed using gene products identified from in vitro work are frequently not reproduced in vivo. Our journal is particularly interested in studies on genetically engineered model organisms (C. elegans, Drosophila, mouse), in which alterations in key molecules underlying cellular and synaptic function and plasticity produce defined anatomical, physiological and behavioral changes. In the mouse, genetic alterations limited to particular neural circuits (olfactory bulb, motor cortex, cortical layers, hippocampal subfields, cerebellum), preferably regulated in time and on demand, are of special interest, as they sidestep potential compensatory developmental effects.