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Cigarette smoke and nicotine effect on human mesenchymal stromal cell wound healing and osteogenic differentiation capacity.
Heikkinen, Janne; Tanner, Tarja; Bergmann, Ulrich; Palosaari, Sanna; Lehenkari, Petri.
Afiliação
  • Heikkinen J; Research Unit of Translational Medicine, Faculty of Medicine, University of Oulu, Oulu, Finland.
  • Tanner T; Research Unit of Oral Health Sciences, University of Oulu, Oulu, Finland.
  • Bergmann U; Dental Training Clinic, Oulu, Finland.
  • Palosaari S; Proteomics and Protein Analysis, Biocenter Oulu, University of Oulu, Oulu, Finland.
  • Lehenkari P; Research Unit of Translational Medicine, Faculty of Medicine, University of Oulu, Oulu, Finland.
Tob Induc Dis ; 222024.
Article em En | MEDLINE | ID: mdl-38496254
ABSTRACT

INTRODUCTION:

Mesenchymal stromal cells (MSCs) play a crucial role in promoting tissue regeneration and healing, particularly in bone tissue. Both smoking and nicotine use are known to delay and inhibit the healing process in patients. This study aims at delineating these cellular effects by comparing the impact of nicotine alone to cigarette smoke with equivalent nicotine content, and shedding light on potential differences in the healing process.

METHODS:

We examined how cigarette smoke and nicotine affect the migration, proliferation, and osteogenic differentiation of human patient-derived MSCs in vitro, as well as the secretion of cytokines IL-6 and IL-8. We measured nicotine concentration of the cigarette smoke extract (CSE) to clarify the role of the nicotine in the effect of the cigarette smoke.

RESULTS:

MSCs exposed to nicotine-concentration-standardized CSE exhibited impaired wound healing capability, and at high concentrations, increased cell death. At lower concentrations, CSE dose-dependently impaired migration, proliferation, and osteogenic differentiation, and increased IL-8 secretion. Nicotine impaired proliferation and decreased PINP secretion. While there was a trend for elevated IL-6 levels by nicotine in undifferentiated MSCs, these changes were not statistically significant. Exposure of MSCs to equivalent concentrations of nicotine consistently elicited stronger responses by CSE and had a more pronounced effect on all studied parameters. Our results suggest that the direct effect of cigarette smoke on MSCs contributes to impaired MSC function, that adds to the nicotine effects.

CONCLUSIONS:

Cigarette smoke extract reduced the migration, proliferation, and osteogenic differentiation in MSCs in vitro, while nicotine alone reduced proliferation. Cigarette smoke impairs the osteogenic and regenerative ability of MSCs in a direct cytotoxic manner. Cytotoxic effect of nicotine alone impairs regenerative ability of MSCs, but it only partly explains cytotoxic effects of cigarette smoke. Direct effect of cigarette smoke, and partly nicotine, on MSCs could contribute to the smoking-related negative impact on long-term bone health, especially in bone healing.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Tob Induc Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Finlândia

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Idioma: En Revista: Tob Induc Dis Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Finlândia