Predicting pulmonary fibrosis in humans after exposure to multi-walled carbon nanotubes (MWCNTs)

被引:39
作者
Sharma, Monita [1 ]
Nikota, Jake [2 ]
Halappanavar, Sabina [2 ]
Castranova, Vincent [3 ]
Rothen-Rutishauser, Barbara [4 ]
Clippinger, Amy J. [1 ]
机构
[1] PETA Int Sci Consortium Ltd, London, England
[2] Hlth Canada, Environm Hlth Sci & Res Bur, Ottawa, ON K1A 0L2, Canada
[3] W Virginia Univ, Sch Pharm, Morgantown, WV 26506 USA
[4] Univ Fribourg, Adolphe Merkle Inst, CH-1700 Fribourg, Switzerland
关键词
Pulmonary fibrosis; In vitro; Multi-walled carbon nanotubes; MWCNTs; Human lung cells; Profibrotic markers; ALVEOLAR EPITHELIAL-CELLS; IN-VITRO MODEL; INHALATION EXPOSURE; INFLAMMASOME ACTIVATION; SILVER-NANOPARTICLES; MOLECULAR-MECHANISMS; CAPILLARY COCULTURE; FIBROTIC RESPONSE; PRIMARY CULTURE; AIRWAY BARRIER;
D O I
10.1007/s00204-016-1742-7
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The increased production and use of multi-walled carbon nanotubes (MWCNTs) in a diverse array of consumer, medical, and industrial applications have raised concerns about potential human exposure to these materials in the workplace and ambient environments. Inhalation is a primary route of exposure to MWCNTs, and the existing data indicate that they are potentially hazardous to human health. While a 90-day rodent inhalation test (e.g., OECD Test No. 413: subchronic inhalation toxicity: 90-day study or EPA Health Effects Test Guidelines OPPTS 870.3465 90-day inhalation toxicity) is recommended by the U.S. Environmental Protection Agency Office of Pollution Prevention and Toxics for MWCNTs (and other CNTs) if they are to be commercially produced (Godwin et al. in ACS Nano 9:3409-3417, 2015), this test is time and cost-intensive and subject to scientific and ethical concerns. As a result, there has been much interest in transitioning away from studies on animals and moving toward human-based in vitro and in silico models. However, given the multiple mechanisms of toxicity associated with subchronic exposure to inhaled MWCNTs, a battery of non-animal tests will likely be needed to evaluate the key endpoints assessed by the 90-day rodent study. Pulmonary fibrosis is an important adverse outcome related to inhalation exposure to MWCNTs and one that the non-animal approach should be able to assess. This review summarizes the state-of-the-science regarding in vivo and in vitro toxicological methods for predicting MWCNT-induced pulmonary fibrosis.
引用
收藏
页码:1605 / 1622
页数:18
相关论文
共 98 条
[1]   ASBESTOS-RELATED PLEURAL AND PARENCHYMAL FIBROSIS - DETECTION WITH HIGH-RESOLUTION CT [J].
ABERLE, DR ;
GAMSU, G ;
RAY, CS ;
FEUERSTEIN, IM .
RADIOLOGY, 1988, 166 (03) :729-734
[2]   THE ROLE OF IRON IMPURITIES IN THE TOXIC EFFECTS EXERTED BY SHORT MULTIWALLED CARBON NANOTUBES (MWCNT) IN MURINE ALVEOLAR MACROPHAGES [J].
Aldieri, E. ;
Fenoglio, I. ;
Cesano, F. ;
Gazzano, E. ;
Gulino, G. ;
Scarano, D. ;
Attanasio, A. ;
Mazzucco, G. ;
Ghigo, D. ;
Fubini, B. .
JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES, 2013, 76 (18) :1056-1071
[3]   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
[4]   Dendritic cell functional properties in a three-dimensional tissue model of human lung mucosa [J].
Anh Thu Nguyen Hoang ;
Chen, Puran ;
Juarez, Julius ;
Sachamitr, Patty ;
Billing, Bo ;
Bosnjak, Lidija ;
Dahlen, Barbro ;
Coles, Mark ;
Svensson, Mattias .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2012, 302 (02) :L226-L237
[5]   An optimized in vitro model of the respiratory tract wall to study particle cell interactions [J].
Blank, Fabian ;
Rothen-Rutishauser, Barbara M. ;
Schurch, Samuel ;
Gehr, Peter .
JOURNAL OF AEROSOL MEDICINE-DEPOSITION CLEARANCE AND EFFECTS IN THE LUNG, 2006, 19 (03) :392-405
[6]   Breaking the In Vitro Alveolar Type II Cell Proliferation Barrier while Retaining Ion Transport Properties [J].
Bove, Peter F. ;
Dang, Hong ;
Cheluvaraju, Chaitra ;
Jones, Lisa C. ;
Liu, Xuefeng ;
O'Neal, Wanda K. ;
Randell, Scott H. ;
Schlegel, Richard ;
Boucher, Richard C. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2014, 50 (04) :767-776
[7]   Effects and uptake of gold nanoparticles deposited at the air-liquid interface of a human epithelial airway model [J].
Brandenberger, C. ;
Rothen-Rutishauser, B. ;
Muehlfeld, C. ;
Schmid, O. ;
Ferron, G. A. ;
Maier, K. L. ;
Gehr, P. ;
Lenz, A. -G. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2010, 242 (01) :56-65
[8]   Quantitative Evaluation of Cellular Uptake and Trafficking of Plain and Polyethylene Glycol-Coated Gold Nanoparticles [J].
Brandenberger, Christina ;
Muehlfeld, Christian ;
Ali, Zulqurnain ;
Lenz, Anke-Gabriele ;
Schmid, Otmar ;
Parak, Wolfgang J. ;
Gehr, Peter ;
Rothen-Rutishauser, Barbara .
SMALL, 2010, 6 (15) :1669-1678
[9]   An in vitro study of the potential of carbon nanotubes and nanofibres to induce inflammatory mediators and frustrated phagocytosis [J].
Brown, D. M. ;
Kinloch, I. A. ;
Bangert, U. ;
Windle, A. H. ;
Walter, D. M. ;
Walker, G. S. ;
Scotchford, C. A. ;
Donaldson, K. ;
Stone, V. .
CARBON, 2007, 45 (09) :1743-1756
[10]   PPARγ agonists inhibit TGF-β induced pulmonary myofibroblast differentiation and collagen production:: implications for therapy of lung fibrosis [J].
Burgess, HA ;
Daugherty, LE ;
Thatcher, TH ;
Lakatos, HF ;
Ray, DM ;
Redonnet, M ;
Phipps, RP ;
Sime, PJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2005, 288 (06) :L1146-L1153