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单细胞RNA测序揭示了暴露于食品添加剂(E171)二氧化钛后异质性免疫细胞反应。

Single-cell RNA sequencing uncovers heterogenous immune cell responses upon exposure to food additive (E171) titanium dioxide.

作者信息

Perumalsamy Haribalan, Xiao Xiao, Han Hyoung-Yun, Oh Jung-Hwa, Yoon Seokjoo, Heo Min Beom, Lee Tae Geol, Kim Hyun-Yi, Yoon Tae-Hyun

机构信息

Institute for Next Generation Material Design, Hanyang University, Seoul, 04763, Republic of Korea.

Research Institute for Convergence of Basic Science, Hanyang University, Seoul, 04763, South Korea.

出版信息

J Nanobiotechnology. 2024 Dec 19;22(1):765. doi: 10.1186/s12951-024-03036-9.

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.

摘要

食品添加剂二氧化钛(E171 TiO)在多个领域(食品、制药和化妆品)的预期应用促使人们对其进行适当的细胞毒性和转录组评估。有趣的是,较小尺寸的E171 TiO能够在血液中转运,并通过激活免疫系统引发多种免疫反应,这种反应可能是促炎的,也可能是免疫抑制的。然而,在接触食品添加剂E171 TiO后,其在异质性免疫系统中的细胞或免疫反应仍有待阐明。为此,我们使用雄性Sprague-Dawley大鼠,通过无创气管内滴注给予E171 TiO(每天5 mg/kg体重),持续13周。在4周的恢复期后,收集处理组和未处理组的3 mL血液样本进行单细胞RNA测序分析。首先,粒细胞G1通过上调参与促炎细胞因子介导的细胞毒性的基因激活先天性免疫反应。而自然杀伤细胞(NK细胞)根据其亚群发挥不同作用,其中NK1显著抑制细胞毒性,而NK2和NK3亚群分别激活前B细胞群体并抑制T细胞介导的细胞毒性。自然杀伤T细胞1(NKT_1)激活先天性炎症反应,这通过细胞毒性CD8 + T杀伤细胞的抑制得到证实。同样,NKT_2细胞通过释放溶解颗粒和抑制主要组织相容性复合体I(MHC-I)复合物来促进炎症反应,以阻止细胞毒性T杀伤细胞反应。相反,NKT_3通过释放抗炎细胞因子抑制炎症反应,表明NKT亚群的功能异质性。MHC-I或MHC-II复合物与T细胞亚群的形成既未导致B细胞和T细胞功能障碍,也未抑制细胞毒性T杀伤细胞,从而抑制适应性免疫反应。总体而言,我们的研究提供了一种创新的高维方法,通过确保对E171 TiO免疫反应的精确评估,在复杂的异质细胞环境中揭示单细胞水平上每种细胞类型的免疫和转录组反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e78/11657454/a9513fe491c7/12951_2024_3036_Fig1_HTML.jpg

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