Method Article

Using Nicotine in a Silica-Exposed Mouse Model to Promote Lung Epithelial-Mesenchymal Transition

DOI:

10.3791/65127

March 3rd, 2023

In This Article

Summary

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This study describes a mouse model to study the synergistic effect of nicotine on the progression of pulmonary fibrosis in experimental silicosis mice. The dual-exposure mouse model simulates the pathological progression in the lung after simultaneous exposure to nicotine and silica. The methods described are simple and highly reproducible.

Abstract

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Smoking and exposure to silica are common among occupational workers, and silica is more likely to injure the lungs of smokers than non-smokers. The role of nicotine, the primary addictive ingredient in cigarettes, in silicosis development is unclear. The mouse model employed in this study was simple and easily controlled, and it effectively simulated the effects of chronic nicotine ingestion and repeated exposure to silica on lung fibrosis through epithelial-mesenchymal transition in human beings. In addition, this model can help in the direct study of the effects of nicotine on silicosis while avoiding the effects of other components in cigarette smoke.

After environmental adaptation, mice were injected subcutaneously with 0.25 mg/kg nicotine solution into the loose skin over the neck every morning and evening at 12 h intervals over 40 days. Additionally, crystalline silica powder (1-5 µm) was suspended in normal saline, diluted to a suspension of 20 mg/mL, and dispersed evenly using an ultrasonic water bath. The isoflurane-anesthetized mice inhaled 50 µL of this silica dust suspension through the nose and were awoken via chest massage. Silica exposure was administrated daily on days 5-19.

The double-exposed mouse model was exposed to nicotine and then silica, which matches the exposure history of workers who are exposed to both harmful factors. In addition, nicotine promoted pulmonary fibrosis through epithelial-mesenchymal transformation (EMT) in mice. This animal model can be used to study the effects of multiple factors on the development of silicosis.

Introduction

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Silica exposure in workers is inevitable in some occupational settings, and once exposed to silica, the deterioration progresses even after removal from the environment. In addition, most of these workers smoke, and traditional cigarettes contain thousands of chemicals, with the key addictive component being nicotine1. E-cigarettes are becoming increasingly popular in younger age groups2; these e-cigarettes act as a nicotine delivery system and increase nicotine access, thus increasing lung susceptibility and pneumonia3. Cigarette smoke also accelerates pulmonary fibrosis in bleomycin-exposed mice....

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Protocol

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All procedures were conducted according to the guidelines issued by the National Institutes of Health's Guide for the Care and Use of Laboratory Animals (the 8th edition of the NRC) and were approved by Anhui University of Science and Technology Animal Ethics Committee.

1. Animal preparation

  1. House 32 male C57/BL6 mice aged 8 weeks in a laboratory with a 12 h light/dark cycle. Ensure that the mice have free access to food and water.
  2. After 2 weeks of acclimation to the environment, when the 10 week old mice weigh 23-26 g, use random numbers generated by a computer to randomly group the animals withou....

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Results

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A mouse model to study nicotine combined with silica exposure was established to investigate the potential role of nicotine in the progression of silicosis in mice. Figure 1 depicts the experimental procedure for using a dual-exposure mouse model, which paired a nicotine injection with the nasal instillation of a silica suspension. The pathological changes of the mice in each group were observed using HE staining. The mice exposed to nicotine combined with silica had significantly more sever.......

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Discussion

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A dual-exposure animal model is necessary to investigate the role and the potential mechanisms of concurrent exposure to nicotine and crystalline silicon dioxide. This model was achieved in this work through the subcutaneous injection of nicotine and the nasal drip of silica. To ensure a successful nicotine injection, the operator has to become familiar with grasping the mice, as grasping the skin at the back of the neck could be painful for them. Therefore, allowing the mice to adapt gradually to the grasping is importa.......

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Disclosures

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All authors declare they have no conflicts of interest.

Acknowledgements

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This study was supported by the University Synergy Innovation Program of Anhui Province (GXXT-2021-077) and the Anhui University of Science and Technology Graduate Innovation Fund (2021CX2120).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
10% formalin neutral fixativeNanchang Yulu Experimental Equipment Co.
alcohol disinfectantXintai Kanyuan Disinfection Products Co.
BSA, Fraction VBeyotime BiotechnologyST023-200g
CD206 Monoclonal antibodyProteintech60143-1-IG
Citrate Antigen Retrieval Solutionbiosharp life scienceBL619A
dimethyl benzeneWest Asia Chemical Technology (Shandong) Co
Enhanced BCA Protein Assay KitBeyotime BiotechnologyP0009
GAPDH Polyclonal antibodyProteintech10494-1-AP
Hematoxylin and Eosin (H&E)Beyotime BiotechnologyC0105S
HRP substrateMillipore CorporationP90720
HRP-conjugated Affinipure Goat Anti-Mouse IgG(H+L)ProteintechSA00001-1
HRP-conjugated Affinipure Goat Anti-Rabbit IgG(H+L)ProteintechSA00001-2
ImmPACT[R] DAB EqV Peroxidase (HRP) SubstrateVector LaboratoriesSK-4103-100
Masson's Trichrome Stain KitSolarbioG1340
MethanolMacklin
NicotineSigmaN-3876
phosphate buffered saline (PBS) BiosharpBL601A
Physiological saline The First People's Hospital of Huainan City
PMSFBeyotime BiotechnologicalST505
Positive fluorescence microscopeOlympusCorporationBX53+DP74
Prestained Color Protein Molecular Weight Marker, or Prestained Color Protein LadderBeyotime BiotechnologyP0071
PVDF membranesMillipore3010040001
RIPA Lysis BufferBeyotime BiotechnologyP0013B
SDS-PAGE gel preparation kitBeyotime BiotechnologyP0012A
Silicon dioxideSigma#BCBV6865
TGF-βBiossbs-0086R
Vimentin Polyclonal antibodyProteintech10366-1-AP
Name of Material/ EquipmentCompanyCatalog Number
0.5 mL TubeBiosharpBS-05-M
Oscillatory thermostatic metal bathAbson
Paraffin Embedding MachinePrecision (Changzhou) Medical Equipment Co.PBM-A
Paraffin SlicerJinhua Kratai Instruments Co.
PipettesEppendorf
Polarized light microscopeOlympusBX51
Precision BalanceAcculabALC-110.4
RODI IOT intelligent multifunctional water purification systemRSJRODI-220BN
Scilogex SK-D1807-E 3D ShakerScilogex
Small animal anesthesia machineAnhui Yaokun Biotech Co., Ltd.ZL-04A
Universal Pipette TipsKIRGENKG1011
Universal Pipette TipsKIRGENKG1212
Universal Pipette TipsKIRGENKG1313
Vortex Mixers VWR
Name of Material/ Equipment
Adobe Illustrator
ImageJ
Photoshop
Prism7.0

References

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  1. Wonnacott, S. Presynaptic nicotinic ACh receptors. Trends in Neurosciences. 20 (2), 92-98 (1997).
  2. Berry, K., et al. Association of electronic cigarette use with subsequent initiation of tobacco cigarettes in US youths. JAMA Network Open.

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Tags

Nicotine ExposureSilica Mouse ModelLung FibrosisEpithelial Mesenchymal TransitionPulmonary FibrosisSubcutaneous InjectionNasal Silica ExposureImmunohistochemical StainingCollagen DepositionTGF Beta One

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