Rosette nanotubes alter IgE-Mediated degranulation in the rat basophilic leukemia (RBL)-2H3 cell line

From National Research Council Canada

DOIResolve DOI: https://doi.org/10.1093/toxsci/kfv166
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Name affiliation
  1. National Research Council of Canada. National Institute for Nanotechnology
FormatText, Article
Journal titleToxicological Sciences
ISSN1096-6080
1096-0929
Volume148
Issue1
Pages108–120
Subjectdegranulation; nanotoxicology; inflammation; self-assembly; rosette nanotubes
Abstract
In this study, the effects of rosette nanotube (RNT) exposure on immune cell viability and function were investigated in vitro using the rat basophilic leukemia (RBL)-2H3 cell line. RBL-2H3 viability was decreased in a dose- and time-dependent manner after lysine-functionalized RNT (K-RNT) exposure. In addition, K-RNTs had a significant effect on RBL-2H3 degranulation. When K-RNT exposure was concurrent with IgE sensitization, 50 and 100 mg l−1 K-RNTs elicited a heightened degranulatory response compared with IgE alone. Exposure to 50 and 100 mg l−1 K-RNTs also caused degranulation in RBL-2H3 cells not sensitized with IgE (0 ng ml−1 IgE). Furthermore, in cells preexposed to K-RNTs for 2 h and subsequently washed, sensitized, and stimulated with IgE, a potentiated degranulatory response was observed. Using confocal laser scanning microscopy and a fluorescein isothiocyanate (FITC)-functionalized RNT construct (termed FITC1/TBL19-RNT), we demonstrated a strong and direct affiliation between RNTs and RBL-2H3 cell membranes. We also demonstrated cellular internalization of RNTs after 2 h of exposure. Together, these data demonstrate that RNTs may affiliate with the cellular membrane of RBL-2H3 cells and can be internalized. These interactions can affect viability and alter the ability of these cells to elicit IgE-FcεR mediated degranulation.
Publication date
PublisherOxford University Press
LanguageEnglish
Peer reviewedYes
NPARC number23001601
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Record created2017-03-09
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