Acute exposure to electronic cigarette components alters mRNA expression of pre-osteoblasts.


Journal

FASEB journal : official publication of the Federation of American Societies for Experimental Biology
ISSN: 1530-6860
Titre abrégé: FASEB J
Pays: United States
ID NLM: 8804484

Informations de publication

Date de publication:
15 Sep 2024
Historique:
revised: 01 08 2024
received: 03 10 2023
accepted: 16 08 2024
medline: 1 9 2024
pubmed: 31 8 2024
entrez: 30 8 2024
Statut: ppublish

Résumé

The use of traditional nicotine delivery products such as tobacco has long been linked to detrimental health effects. However, little work to date has focused on the emerging market of aerosolized nicotine delivery known as electronic nicotine delivery systems (ENDS) or electronic cigarettes, and their potential for new effects on human health. Challenges studying these devices include heterogeneity in the formulation of the common components of most available ENDS, including nicotine and a carrier (commonly composed of propylene glycol and vegetable glycerin, or PG/VG). In the present study, we report on experiments interrogating the effects of major identified components in e-cigarettes. Specifically, the potential concomitant effects of nicotine and common carrier ingredients in commercial "vape" products are explored in vitro to inform the potential health effects on the craniofacial skeleton through novel vectors as compared to traditional tobacco products. MC3T3-E1 murine pre-osteoblast cells were cultured in vitro with clinically relevant liquid concentrations of nicotine, propylene glycol (PG), vegetable glycerin (VG), Nicotine+PG/VG, and the vape liquid of a commercial product (Juul). Cells were treated acutely for 24 h and RNA-Seq was utilized to determine segregating alteration in mRNA signaling. Influential gene targets identified with sparse partial least squares discriminant analysis (sPLS-DA) implemented in mixOmics were assessed using the PANTHER Classification system for molecular functions, biological processes, cellular components, and pathways of effect. Additional endpoint functional analyses were used to confirm cell cycle changes. The initial excitatory concentration (EC50) studied defined a target concentration of carrier PG/VG liquid that altered the cell cycle of the calvarial cells. Initial sPLS-DA analysis demonstrated the segregation of nicotine and non-nicotine exposures utilized in our in vitro modeling. Pathway analysis suggests a strong influence of nicotine exposures on cellular processes including metabolic processes and response to stimuli including autophagic flux. Further interrogation of the individual treatment conditions demonstrated segregation by treatment modality (Control, Nicotine, Carrier (PG+VG), Nicotine+PG/VG) along three dimensions best characterized by: latent variable 1 (PLSDA-1) showing strong segregation based on nicotine influence on cellular processes associated with cellular adhesion to collagen, osteoblast differentiation, and calcium binding and metabolism; latent variable 2 (PLSDA-2) showing strong segregation of influence based on PG+VG and Control influence on cell migration, survival, and cycle regulation; and latent variable 3 (PLSDA-3) showing strong segregation based on Nicotine and Control exposure influence on cell activity and growth and developmental processes. Further, gene co-expression network analysis implicates targets of the major pathway genes associated with bone growth and development, particularly craniofacial (FGF, Notch, TGFβ, WNT) and analysis of active subnetwork pathways found these additionally overrepresented in the Juul exposure relative to Nicotine+PG/VG. Finally, experimentation confirmed alterations in cell count, and increased evidence of cell stress (markers of autophagy), but no alteration in apoptosis. These data suggest concomitant treatment with Nicotine+PG/VG drives alterations in pre-osteoblast cell cycle signaling, specifically transcriptomic targets related to cell cycle and potentially cell stress. Although we suspected cell stress and well as cytotoxic effects of Nicotine+PG/VG, no great influence on apoptotic factors was observed. Further RNA-Seq analysis allowed for the direct interrogation of molecular targets of major pathways involved in bone and craniofacial development, each demonstrating segregation (altered signaling) due to e-cigarette-type exposure. These data have implications directed toward ENDS formulation as synergistic effects of Nicotine+PG/VG are evidenced here. Thus, future research will continue to interrogate how varied formulation of Nicotine+PG/VG affects overall cell functions in multiple vital systems.

Identifiants

pubmed: 39213037
doi: 10.1096/fj.202302014RRR
doi:

Substances chimiques

Nicotine 6M3C89ZY6R
RNA, Messenger 0
Propylene Glycol 6DC9Q167V3

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e70017

Subventions

Organisme : NIDCR NIH HHS
ID : R03 DE026192
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002733
Pays : United States
Organisme : HHS | NIH | National Institute of General Medical Sciences (NIGMS)
ID : UL1TR002733
Organisme : HHS | NIH | National Institute of Dental and Craniofacial Research (NIDCR)
ID : R03DE026192

Informations de copyright

© 2024 The Author(s). The FASEB Journal published by Wiley Periodicals LLC on behalf of Federation of American Societies for Experimental Biology.

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Auteurs

Shareef M Dabdoub (SM)

Division of Biostatistics and Computational Biology, College of Dentistry, University of Iowa, Iowa City, Iowa, USA.
Department of Periodontics, College of Dentistry, University of Iowa, Iowa City, Iowa, USA.

Ashley Greenlee (A)

Biomedical Sciences Graduate Program, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

George Abboud (G)

Undergraduate Biomedical Sciences Major, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

Lexie Brengartner (L)

Undergraduate Biomedical Sciences Major, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

Eryn Zuiker (E)

Biomedical Sciences Graduate Program, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

Matthew W Gorr (MW)

Division of Cardiac Surgery, Department of Surgery, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

Loren E Wold (LE)

Division of Cardiac Surgery, Department of Surgery, College of Medicine, The Ohio State University, Columbus, Ohio, USA.

Purnima S Kumar (PS)

Department of Periodontics and Oral Medicine, School of Dentistry, University of Michigan, Ann Arbor, Michigan, USA.

James Cray (J)

Department of Biomedical Education and Anatomy, College of Medicine, The Ohio State University, Columbus, Ohio, USA.
Division of Biosciences, College of Dentistry, The Ohio State University, Columbus, Ohio, USA.
Division of Orthodontics, College of Dentistry, The Ohio State University, Columbus, Ohio, USA.

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