Published May 2019 | Version v1
Journal article

Stimulation of eryptosis by broad-spectrum insect repellent N,N-Diethyl-3-methylbenzamide (DEET)

  • 1. Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Saud University, Riyadh 11433 (Saudi Arabia)
  • 2. Division of Hematology/Oncology, Department of Medicine, Brody School of Medicine, East Carolina University, Greenville, NC 27834 (United States)
  • 3. Department of Psychology, Thomas Harriot College of Arts and Sciences, East Carolina University, Greenville, NC 27834 (United States)
  • 4. Department of Microbiology & Immunology, Brody School of Medicine, East Carolina University, Greenville, NC 27834 (United States)
  • 5. Lineberger Comprehensive Cancer Center, University of North Carolina-Chapel Hill, Chapel Hill, NC 27599 (United States)

Description

Highlights: • DEET possesses a weak hemolytic potential in human erythrocytes. • DEET induces eryptosis characterized by cell membrane scrambling with phosphatidylserine (PS) externalization • DEET-induced premature cell death is accompanied by cell shrinkage and dysregulated calcium influx. • DEET-induced PS exposure is not ameliorated by extracellular calcium removal nor by intracellular calcium chelation. • Suicidal erythrocyte death caused by DEET is not mediated through oxidative stress or a specific signaling pathway. -- Abstract: N,N-Diethyl-3-methylbenzamide (DEET) is the most widely used insect repellent in the world. Adverse effects following DEET exposure are well documented. Moreover, DEET has been shown to possess cytotoxic and apoptotic properties in nucleated cells. Although red blood cells (RBCs) lack intracellular organelles, they nevertheless undergo programmed cell death termed eryptosis. Compromised RBC health contributes to the development of anemia; a condition affecting 25% of the global population. This study investigated the interaction between DEET and human RBCs, and explored accompanying biochemical and molecular alterations. RBCs at 5% hematocrit were incubated in presence and absence of 1–5 mM (0.02%–0.1%) of DEET for 6 h at 37 °C. Hemolysis was spectrophotometrically determined by hemoglobin release, while major eryptotic events were analyzed by flow cytometer. Phosphatidylserine (PS) exposure was detected with Annexin-V-FITC, cell volume by forward scatter (FSC) of light, intracellular calcium with Fluo-3/AM, and reactive oxygen species with 2′,7′-dichlorodihydrofluorescein diacetate (H2DCFDA). DEET caused slight hemolysis at 4 and 5 mM, and significantly increased Annexin-V-FITC and Fluo3 fluorescence, with reduced FSC at 5 mM. Removal of extracellular Ca2+ abolished DEET-induced Fluo3 fluorescence but had no effect on Annexin-V binding. Importantly, blockade of eryptotic signaling mediators p38 MAPK, caspases, protein kinase C, casein kinase 1, or necroptotic kinases receptor-interacting protein 1 and mixed lineage kinase domain-like protein, with small molecule inhibitors, did not ameliorate DEET-mediated PS externalization. In conclusion, DEET elicits suicidal erythrocyte death; an event characterized by loss of membrane asymmetry, cell shrinkage, and elevations in intracellular Ca2+ mainly through dysregulated Ca2+ influx.

Additional details

Identifiers

DOI
10.1016/j.taap.2019.03.011;
PII
S0041008X19300936;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
370
Journal Page Range
p. 36-43
ISSN
0041-008X
CODEN
TXAPA9

Optional Information

Copyright
Copyright (c) 2019 Elsevier Inc. All rights reserved.