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Single-cell RNA Sequencing Uncovers Heterogenous Immune Cell Responses Upon Exposure to Food Additive (E171) Titanium Dioxide

Overview
Publisher Biomed Central
Specialty Biotechnology
Date 2024 Dec 19
PMID 39696498
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Abstract

The prospective use of food additive titanium dioxide (E171 TiO) in a variety of fields (food, pharmaceutics, and cosmetics) prompts proper cellular cytotoxicity and transcriptomic assessment. Interestingly, smaller-sized E171 TiO can translocate in bloodstream and induce a diverse immunological response by activating the immune system, which can be either pro-inflammatory or immune-suppressive. Nevertheless, their cellular or immunologic responses in a heterogeneous population of the immune system following exposure of food additive E171 TiO is yet to be elucidated. For this purpose, we have used male Sprague-Dawley rats to deliver E171 TiO (5 mg/kg bw per day) via non-invasive intratracheal instillation for 13 weeks. After the 4 weeks recovery period, 3 mL of blood samples from both treated and untreated groups were collected for scRNAseq analysis. Firstly, granulocyte G1 activated innate immune response through the upregulation of genes involved in pro-inflammatory cytokine mediated cytotoxicity. Whereas NK cells resulted in heterogeneity role depending on the subsets where NK1 significantly inhibited cytotoxicity, whereas NK2 and NK3 subsets activated pro-B cell population & inhibited T cell mediated cytotoxicity respectively. While NKT_1 activated innate inflammatory responses which was confirmed by cytotoxic CD8+ T killer cell suppression. Similarly, NKT_2 cells promote inflammatory response by releasing lytic granules and MHC-I complex inhibition to arrest cytotoxic T killer cell responses. Conversely, NKT_3 suppressed inflammatory response by release of anti-inflammatory cytokines suggesting the functional heterogeneity of NKT subset. The formation of MHC-I or MHC-II complexes with T-cell subsets resulted in neither B and T cell dysfunction nor cytotoxic T killer cell inhibition suppressing adaptive immune response. Overall, our research offers an innovative high-dimensional approach to reveal immunological and transcriptomic responses of each cell types at the single cell level in a complex heterogeneous cellular environment by reassuring a precise assessment of immunological response of E171 TiO.

References
1.
Lee Y, Starrett G, Lee S, Yang R, Henzler C, Jameson S . Lineage-Specific Effector Signatures of Invariant NKT Cells Are Shared amongst γδ T, Innate Lymphoid, and Th Cells. J Immunol. 2016; 197(4):1460-70. PMC: 4976040. DOI: 10.4049/jimmunol.1600643. View

2.
Mikelez-Alonso I, Magadan S, Gonzalez-Fernandez A, Borrego F . Natural killer (NK) cell-based immunotherapies and the many faces of NK cell memory: A look into how nanoparticles enhance NK cell activity. Adv Drug Deliv Rev. 2021; 176:113860. DOI: 10.1016/j.addr.2021.113860. View

3.
Luo Y, Chang L, Lin P . Metal-Based Nanoparticles and the Immune System: Activation, Inflammation, and Potential Applications. Biomed Res Int. 2015; 2015:143720. PMC: 4466342. DOI: 10.1155/2015/143720. View

4.
Gotthardt D, Putz E, Grundschober E, Prchal-Murphy M, Straka E, Kudweis P . STAT5 Is a Key Regulator in NK Cells and Acts as a Molecular Switch from Tumor Surveillance to Tumor Promotion. Cancer Discov. 2016; 6(4):414-29. DOI: 10.1158/2159-8290.CD-15-0732. View

5.
Baranowska-Wojcik E, Szwajgier D, Winiarska-Mieczan A . A review of research on the impact of E171/TiO NPs on the digestive tract. J Trace Elem Med Biol. 2022; 72:126988. DOI: 10.1016/j.jtemb.2022.126988. View