TY  - JOUR
A1  - Brachner, Andreas
A1  - Fragouli, Despina
A1  - Duarte, Iola F.
A1  - Farias, Patricia M. A.
A1  - Dembski, Sofia
A1  - Ghosh, Manosij
A1  - Barisic, Ivan
A1  - Zdzieblo, Daniela
A1  - Vanoirbeek, Jeroen
A1  - Schwabl, Philipp
A1  - Neuhaus, Winfried
T1  - Assessment of human health risks posed by nano-and microplastics is currently not feasible
JF  - International Journal of Environmental Research and Public Health
N2  - The exposure of humans to nano-and microplastic particles (NMPs) is an issue recognized as a potential health hazard by scientists, authorities, politics, non-governmental organizations and the general public. The concentration of NMPs in the environment is increasing concomitantly with global plastic production and the usage of plastic materials. NMPs are detectable in numerous aquatic organisms and also in human samples, therefore necessitating a risk assessment of NMPs for human health. So far, a comprehensive risk assessment of NMPs is hampered by limited availability of appropriate reference materials, analytical obstacles and a lack of definitions and standardized study designs. Most studies conducted so far used polystyrene (PS) spheres as a matter of availability, although this polymer type accounts for only about 7% of total plastic production. Differently sized particles, different concentration and incubation times, and various biological models have been used, yielding hardly comparable data sets. Crucial physico-chemical properties of NMPs such as surface (charge, polarity, chemical reactivity), supplemented additives and adsorbed chemicals have been widely excluded from studies, although in particular the surface of NMPs determines the interaction with cellular membranes. In this manuscript we give an overview about the critical parameters which should be considered when performing risk assessments of NMPs, including novel reference materials, taking into account surface modifications (e.g., reflecting weathering processes), and the possible role of NMPs as a substrate and/or carrier for (pathogenic) microbes. Moreover, we make suggestions for biological model systems to evaluate immediate toxicity, long-term effects and the potential of NMPs to cross biological barriers. We are convinced that standardized reference materials and experimental parameters along with technical innovations in (nano)-particle sampling and analytics are a prerequisite for the successful realization of conclusive human health risk assessments of NMPs.
KW  - nanoplastics
KW  - nanoparticles
KW  - microplastics
KW  - microparticles
KW  - human exposure
KW  - biological barriers
KW  - biofilm
KW  - microbe carrier
KW  - toxicity
KW  - neurotoxicity
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-219423
SN  - 1660-4601
VL  - 17
IS  - 23
ER  - 
TY  - JOUR
A1  - Berger, Constantin
A1  - Zdzieblo, Daniela
T1  - Glucose transporters in pancreatic islets
JF  - Pflügers Archiv - European Journal of Physiology
N2  - The fine-tuning of glucose uptake mechanisms is rendered by various glucose transporters with distinct transportcharacteristics. In the pancreatic islet, facilitative diffusion glucose transporters (GLUTs), and sodium-glucosecotransporters (SGLTs) contribute to glucose uptake and represent important components in the glucose-stimulatedhormone release from endocrine cells, therefore playing a crucial role in blood glucose homeostasis. This reviewsummarizes the current knowledge aboutcell type-specific expression profiles as well as proven and putative functionsof distinct GLUT and SGLT family members in the human and rodent pancreatic islet and further discusses their possibleinvolvement in onset and progression ofdiabetes mellitus. In context of GLUTs, we focus on GLUT2, characterizing themain glucose transporter in insulin-secretingβ-cells in rodents. In addition, we discuss recent data proposing that otherGLUT family members, namely GLUT1 and GLUT3, render this task in humans. Finally, we summarize latest infor-mation about SGLT1 and SGLT2 as representatives of the SGLT family that have been reported to be expressed predominantly in the α-cell population with a suggested functional role in the regulation of glucagon release
KW  - Glucose transport
KW  - Pancreatic islet
KW  - β-Cell
KW  - α-Cell
KW  - GLUTs
KW  - SGLTs
Y1  - 2020
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-232738
SN  - 0031-6768
VL  - 472
ER  -