Flavored e-liquids increase cytoplasmic Ca2+levels in airway epithelia

Author:

Rowell Temperance R.12,Keating James E.3,Zorn Bryan T.1,Glish Gary L.3,Shears Stephen B.4,Tarran Robert12

Affiliation:

1. Marsico Lung Institute, University of North Carolina, Chapel Hill, North Carolina

2. Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, North Carolina

3. Department of Chemistry, University of North Carolina, Chapel Hill, North Carolina

4. Laboratory of Signal Transduction, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina

Abstract

E-cigarettes are noncombustible, electronic nicotine-delivery devices that aerosolize an e-liquid, i.e., nicotine, in a propylene glycol-vegetable glycerin vehicle that also contains flavors. While the effects of nicotine are relatively well understood, more information regarding the potential biological effects of the other e-liquid constituents is needed. This is a serious concern, because e-liquids are available in >7,000 distinct flavors. We previously demonstrated that many e-liquids affect cell growth/viability through an unknown mechanism. Since Ca2+is a ubiquitous second messenger that regulates cell growth, we characterized the effects of e-liquids on cellular Ca2+homeostasis. To better understand the extent of this effect, we screened e-liquids for their ability to alter cytosolic Ca2+levels and found that 42 of 100 flavored e-liquids elicited a cellular Ca2+response. Banana Pudding (BP) e-liquid, a representative e-liquid from this group, caused phospholipase C activation, endoplasmic reticulum (ER) Ca2+release, store-operated Ca2+entry (SOCE), and protein kinase C (PKCα) phosphorylation. However, longer exposures to BP e-liquid depleted ER Ca2+stores and inhibited SOCE, suggesting that this e-liquid may alter Ca2+homeostasis by short- and long-term mechanisms. Since dysregulation of Ca2+signaling can cause chronic inflammation, ER stress, and abnormal cell growth, flavored e-cigarette products that can elicit cell Ca2+responses should be further screened for potential toxicity.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute of Environmental Health Sciences

HHS | FDA | Center for Tobacco Products

Publisher

American Physiological Society

Subject

Cell Biology,Physiology (medical),Pulmonary and Respiratory Medicine,Physiology

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