A 3D co-culture of three human cell lines to model the inflamed intestinal mucosa for safety testing of nanomaterials

被引:90
作者
Susewind, Julia [1 ]
Carvalho-Wodarz, Cristiane de Souza [1 ]
Repnik, Urska [3 ]
Collnot, Eva-Maria [1 ,2 ]
Schneider-Daum, Nicole [1 ]
Griffiths, Gareth Wyn [3 ]
Lehr, Claus-Michael [1 ,2 ]
机构
[1] Helmholtz Ctr Infect Res HZI, Helmholtz Inst Pharmaceut Res Saarland HIPS, Dept Drug Delivery, Saarbrucken, Germany
[2] Univ Saarland, Dept Pharm Biopharm & Pharmaceut Technol, D-66123 Saarbrucken, Germany
[3] Univ Oslo, Dept Biosci, Oslo, Norway
关键词
Caco-2; cytotoxicity; intestine; nanoparticles; INFLAMMATORY-BOWEL-DISEASE; IN-VITRO ASSESSMENT; SILVER NANOPARTICLES; DIOXIDE NANOPARTICLES; BARRIER DYSFUNCTION; OXIDATIVE STRESS; TIGHT JUNCTIONS; TOXICITY; EXPOSURE; VIVO;
D O I
10.3109/17435390.2015.1008065
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Oral exposure to nanomaterials is a current concern, asking for innovative biological test systems to assess their safety, especially also in conditions of inflammatory disorders. Aim of this study was to develop a 3D intestinal model, consisting of Caco-2 cells and two human immune cell lines, suitable to assess nanomaterial toxicity, in either healthy or diseased conditions. Human macrophages (THP-1) and human dendritic cells (MUTZ-3) were embedded in a collagen scaffold and seeded on the apical side of transwell inserts. Caco-2 cells were seeded on top of this layer, forming a 3D model of the intestinal mucosa. Toxicity of engineered nanoparticles (NM101 TiO2, NM300 Ag, Au) was evaluated in non-inflamed and inflamed co-cultures, and also compared to non-inflamed Caco-2 monocultures. Inflammation was elicited by IL-1, and interactions with engineered NPs were addressed by different endpoints. The 3D co-culture showed well preserved ultrastructure and significant barrier properties. Ag NPs were found to be more toxic than TiO2 or Au NPs. But once inflamed with IL-1, the co-cultures released higher amounts of IL-8 compared to Caco-2 monocultures. However, the cytotoxicity of Ag NPs was higher in Caco-2 monocultures than in 3D co-cultures. The naturally higher IL-8 production in the co-cultures was enhanced even further by the Ag NPs. This study shows that it is possible to mimic inflamed conditions in a 3D co-culture model of the intestinal mucosa. The fact that it is based on three easily available human cell lines makes this model valuable to study the safety of nanomaterials in the context of inflammation.
引用
收藏
页码:53 / 62
页数:10
相关论文
共 58 条
[1]   Patients with Asthma Demonstrate Airway Inflammation after Exposure to Concentrated Ambient Particulate Matter [J].
Alexis, Neil E. ;
Huang, Yuh Chin T. ;
Rappold, Ana G. ;
Kehrl, Howard ;
Devlin, Robert ;
Peden, David B. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2014, 190 (02) :235-237
[2]   Co-cultures of multiple cell types mimic pulmonary cell communication in response to urban PM10 [J].
Alfaro-Moreno, E. ;
Nawrot, T. S. ;
Vanaudenaerde, B. M. ;
Hoylaerts, M. F. ;
Vanoirbeek, J. A. ;
Nemery, B. ;
Hoet, P. H. M. .
EUROPEAN RESPIRATORY JOURNAL, 2008, 32 (05) :1184-1194
[3]   Nanotoxicology and in vitro studies: The need of the hour [J].
Arora, Sumit ;
Rajwade, Jyutika M. ;
Paknikar, Kishore M. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2012, 258 (02) :151-165
[4]   Effect of surface charge on the colloidal stability and in vitro uptake of carboxymethyl dextran-coated iron oxide nanoparticles [J].
Ayala, Vanessa ;
Herrera, Adriana P. ;
Latorre-Esteves, Magda ;
Torres-Lugo, Madeline ;
Rinaldi, Carlos .
JOURNAL OF NANOPARTICLE RESEARCH, 2013, 15 (08)
[5]   Toxicity of silver nanoparticles-Nanoparticle or silver ion? [J].
Beer, Christiane ;
Foldbjerg, Rasmus ;
Hayashi, Yuya ;
Sutherland, Duncan S. ;
Autrup, Herman .
TOXICOLOGY LETTERS, 2012, 208 (03) :286-292
[6]   pH-sensitive nanoparticles for colonic delivery of curcumin in inflammatory bowel disease [J].
Beloqui, Ana ;
Coco, Regis ;
Memvanga, Patrick B. ;
Ucakar, Bernard ;
des Rieux, Anne ;
Preat, Veronique .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2014, 473 (1-2) :203-212
[7]   The Expression and the Cellular Distribution of the Tight Junction Proteins Are Altered in Irritable Bowel Syndrome Patients With Differences According to the Disease Subtype [J].
Bertiaux-Vandaele, Nathalie ;
Youmba, Stephanie Beutheu ;
Belmonte, Liliana ;
Lecleire, Stephane ;
Antonietti, Michel ;
Gourcerol, Guillaume ;
Leroi, Anne-Marie ;
Dechelotte, Pierre ;
Menard, Jean-Francois ;
Ducrotte, Philippe ;
Coeffier, Moise .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2011, 106 (12) :2165-2173
[8]   Patients with inflammatory bowel disease (IBD) reveal increased induction capacity of intracellular interferon-gamma (IFN-γ) in peripheral CD8+ lymphocytes co-cultured with intestinal epithelial cells [J].
Bisping, G ;
Lügering, N ;
Lütke-Brintrup, S ;
Pauels, HG ;
Schürmann, G ;
Domschke, W ;
Kucharzik, T .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 123 (01) :15-22
[9]   Inflammatory responses of a macrophage/epithelial cell co-culture model to mono and mixed infections with Porphyromonas gingivalis, Treponema denticola, and Tannerella forsythia [J].
Bodet, C ;
Chandad, F ;
Grenier, D .
MICROBES AND INFECTION, 2006, 8 (01) :27-35
[10]   Comparison of gene expression profiles in mice liver following intravenous injection of 4 and 100 nm-sized PEG-coated gold nanoparticles [J].
Cho, Wan-Seob ;
Kim, Seungryul ;
Han, Beom Seok ;
Son, Woo Chan ;
Jeong, Jayoung .
TOXICOLOGY LETTERS, 2009, 191 (01) :96-102