Cellular and Molecular Biosciences Faculty, School of Life Sciences, Arizona State University, PO Box 874501, Tempe, AZ 85287-4501, USA.
Cell Biol Toxicol. 2010 Jun;26(3):225-38. doi: 10.1007/s10565-009-9132-z. Epub 2009 Jul 18.
The increasing use of nanomaterials in healthcare and industrial products heightens the possibility of their ingestion by humans, other mammals, and fish. While toxicity of many nanomaterials has recently been studied, reports of non-lethal effects of nanomaterials remain ill-defined. This study investigates possible pathways by which nanoparticles, titanium dioxide (TiO(2)), could cross the epithelium layer by employing both toxicity and mechanistic studies. This study provides evidence that at 10 microg/mL and above, TiO(2) nanoparticles cross the epithelial lining of the intestinal model by transcytosis, albeit at low levels. TiO(2) was able to penetrate into and through the cells without disrupting junctional complexes, as measured by gamma-catenin. To monitor the epithelial integrity, transepithelial electrical resistance (TEER) was employed and determined low concentrations (10 or 100 microg/mL) of TiO(2) do not disrupt epithelial integrity. Live/dead analysis results did not show cell death after exposure to TiO(2). In addition, at 10 microg/mL (and above) TiO(2) nanoparticles begin alteration of both microvillar organization on the apical surface of the epithelium as well as induce a rise in intracellular-free calcium. The latter is a mechanism cells use to respond to extracellular stimuli and may be linked to the alteration of the apical microvilli. Although TiO(2) does not show cell death, the implication of other, non-lethal, effects could lead to undesired outcomes (i.e., disease, malnutrition, shortened life span, etc.).
纳米材料在医疗和工业产品中的应用日益增多,这增加了人类、其他哺乳动物和鱼类摄入它们的可能性。尽管最近已经研究了许多纳米材料的毒性,但纳米材料非致死效应的报告仍然定义不明确。本研究通过毒性和机制研究,调查了纳米颗粒(二氧化钛(TiO(2)))可能通过上皮层的途径。本研究提供的证据表明,在 10μg/mL 及以上浓度时,TiO(2)纳米颗粒通过转胞吞作用穿过肠道模型的上皮衬里,但水平较低。TiO(2)能够穿透细胞而不破坏细胞间连接复合体,如γ-连环蛋白所测量的那样。为了监测上皮完整性,采用了跨上皮电阻(TEER),并确定低浓度(10 或 100μg/mL)的 TiO(2)不会破坏上皮完整性。活/死分析结果显示,暴露于 TiO(2)后没有细胞死亡。此外,在 10μg/mL(及以上)时,TiO(2)纳米颗粒开始改变上皮细胞顶表面的微绒毛组织,并诱导细胞内游离钙升高。后者是细胞对外界刺激做出反应的一种机制,可能与顶微绒毛的改变有关。尽管 TiO(2)没有显示出细胞死亡,但其他非致死效应的影响可能导致不良后果(即疾病、营养不良、寿命缩短等)。