The gut barrier and the fate of engineered nanomaterials: A view from comparative physiology

Meike Van Der Zande*, Anita Jemec Kokalj, David J. Spurgeon, Susana Loureiro, Patrícia V. Silva, Zahra Khodaparast, Damjana Drobne, Nathaniel J. Clark, Nico W. Van Den Brink, Marta Baccaro, Cornelis A.M. Van Gestel, Hans Bouwmeester, Richard D. Handy

*Corresponding author for this work

    Research output: Contribution to JournalArticleAcademicpeer-review

    Abstract

    The structure of the gut barrier and luminal chemistry in non-mammalian vertebrates and invertebrates has been given little attention with respect to the dietary uptake of engineered nanomaterials (ENMs). This review compares the diversity of gut anatomy in selected species used for regulatory toxicity testing, especially in relation to gut lumen chemistry and the behaviour of ENMs, and the gut as a barrier to ENMs. High ionic strength, the presence of divalent ions and organic matter promote particle aggregation in the lumen. The redox chemistry of the gut offers reducing conditions for ENM transformation, and corona formation will depend on the gut contents. Areas of low pH in the gut lumen in several species will promote the dissolution of metallic ENMs. There is a protective unstirred layer over the surface of the epithelium that may concentrate ENMs. Some organisms, especially vertebrates, can slough mucus to remove this adsorbed nanomaterial and lower bioavailability. Invertebrates also have protective layers of cuticle or peritrophic membranes that will modulate ENM uptake. Paracellular uptake of ENMs is unlikely. Transcellular uptake via vesicular-dependent pathways remains the most likely route across the gut epithelium. Most species have receptor-mediated endocytosis pathways and/or macropinocytosis in the gut epithelium. Crucially, many invertebrates have another potential pathway via 'intracellular digestion' uptake routes leading into the gut epithelium, and with gut associated immune cells being a potential route for ENM translocation across the epithelium. The basal lamina provides another barrier prior to the internal compartments of many animals. The features of the gut lumen and epithelium can limit the uptake of ENMs across the gut barrier in vivo, although some ENMs are detected in the tissues. Invertebrates also have the ability for biogenic mineral formation at the nano scale inside tissues. In conclusion, despite the diverse structural anatomies of the gut barrier of animals, some common features in the gut lumen chemistry tend to promote particle aggregation and settling onto the gut surface. The functional anatomy ensures the gut remains a formidable barrier to ENMs, and with some potential novel uptake processes in invertebrates that are not present in vertebrate animals.

    Original languageEnglish
    Pages (from-to)1874-1898
    Number of pages25
    JournalEnvironmental Science: Nano
    Volume7
    Issue number7
    Early online date27 Apr 2020
    DOIs
    Publication statusPublished - Jul 2020

    Funding

    All the authors were funded by the EU H2020 project Nano-FASE (Nanomaterial Fate and Speciation in the Environment; grant no. 646002). SL, PVS and ZK received additional financial support from FCT/MCTES, through national funds, to CESAM (UIDP/50017/2020+UIDB/50017/2020); PVS was awarded with a PhD grant by FCT (SFRH/BD/51571/2014). MvdZ received additional financial support from the Dutch Ministry of Agriculture, Nature and Food Quality (project KB-23-002-005). RH was partly supported by the EU H2020 Nanoharmony project (grant no. 8859231). AJK was funded by Slovenian Research Agency through program P1-0184 Integrative zoology and speleobiology.

    FundersFunder number
    Dutch Ministry of Agriculture, Nature and Food QualityKB-23-002-005
    EU H2020
    EU H2020 Nanoharmony8859231
    FCT/MCTES
    Speciation in the Environment
    Horizon 2020 Framework Programme646002, 885931
    Centro de Estudos Ambientais e Marinhos, Universidade de AveiroUIDP/50017/2020+UIDB/50017/2020
    Javna Agencija za Raziskovalno Dejavnost RS
    Fundació Catalana de TrasplantamentSFRH/BD/51571/2014

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