Literature DB >> 11339625

Silica-induced cytokine release from A549 cells: importance of surface area versus size.

R B Hetland1, P E Schwarze, B V Johansen, T Myran, N Uthus, M Refsnes.   

Abstract

Physical and chemical properties such as structure, composition and surface reactivity determine the biological activity of mineral particles. Long-term exposure to crystalline silica is known to cause persistent pulmonary inflammation leading to adverse health effects. There is less information about the potential health effects of amorphous (noncrystalline) silica. In this study, the inflammatory and cytotoxic potency of crystalline and amorphous silica in relation to particle size and surface area was assessed. Human epithelial lung cells (A549) were exposed to different size fractions of quartz ( aerodynamic diameter 0.5, 2 and 10 microm) and amorphous silica (diameter 0.3 microm). All particles induced increased release of the proinflammatory cytokines interleukin (IL)-6 and IL-8. When cells were exposed to equal masses of quartz, the smallest size fraction was the most potent. These differences, however, disappeared when cytokine release was related to equal surface areas. When amorphous silica and quartz were compared, the amorphous silica was most potent to induce IL - 6 regardless of how exposure was expressed, whereas the smallest size fraction of quartz was the most potent inducer of IL-8. Thus, the surface area seems to be the critical determinant when potency of different sizes of quartz is compared.

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Year:  2001        PMID: 11339625     DOI: 10.1191/096032701676225130

Source DB:  PubMed          Journal:  Hum Exp Toxicol        ISSN: 0960-3271            Impact factor:   2.903


  21 in total

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3.  Nanomaterial interactions with and trafficking across the lung alveolar epithelial barrier: implications for health effects of air-pollution particles.

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Journal:  Air Qual Atmos Health       Date:  2011-03-01       Impact factor: 3.763

4.  The Inflammatory Effect of Iron Oxide and Silica Particles on Lung Epithelial Cells.

Authors:  L J Williams; G R Zosky
Journal:  Lung       Date:  2019-02-14       Impact factor: 2.584

5.  Alveolar epithelial cell processing of nanoparticles activates autophagy and lysosomal exocytosis.

Authors:  Arnold Sipos; Kwang-Jin Kim; Robert H Chow; Per Flodby; Zea Borok; Edward D Crandall
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-05-03       Impact factor: 5.464

6.  The pro-inflammatory effects of low-toxicity low-solubility particles, nanoparticles and fine particles, on epithelial cells in vitro: the role of surface area.

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7.  The phagocytosis and toxicity of amorphous silica.

Authors:  Lindsey M Costantini; Renée M Gilberti; David A Knecht
Journal:  PLoS One       Date:  2011-02-02       Impact factor: 3.240

8.  Differences in gene expression and cytokine production by crystalline vs. amorphous silica in human lung epithelial cells.

Authors:  Timothy N Perkins; Arti Shukla; Paul M Peeters; Jeremy L Steinbacher; Christopher C Landry; Sherrill A Lathrop; Chad Steele; Niki L Reynaert; Emiel F M Wouters; Brooke T Mossman
Journal:  Part Fibre Toxicol       Date:  2012-02-02       Impact factor: 9.400

9.  Interactions of silica nanoparticles with lung epithelial cells and the association to flotillins.

Authors:  Jennifer Kasper; Maria I Hermanns; Christoph Bantz; Olga Koshkina; Thomas Lang; Michael Maskos; Christine Pohl; Ronald E Unger; C James Kirkpatrick
Journal:  Arch Toxicol       Date:  2012-06-06       Impact factor: 5.153

10.  Inflammatory and cytotoxic responses of an alveolar-capillary coculture model to silica nanoparticles: comparison with conventional monocultures.

Authors:  Jennifer Kasper; Maria I Hermanns; Christoph Bantz; Michael Maskos; Roland Stauber; Christine Pohl; Ronald E Unger; James C Kirkpatrick
Journal:  Part Fibre Toxicol       Date:  2011-01-27       Impact factor: 9.400

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