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Updated: May 3, 2026

Measuring Carbon Content in Airway Macrophages Exposed to Carbon-Containing Particulate Matters
Published on: July 12, 2024
Microvesicle-associated microRNA expression is altered upon particulate matter exposure in healthy workers and in
Valentina Bollati1, Laura Angelici, Giovanna Rizzo
1Center of Molecular and Genetic Epidemiology, Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy; Epidemiology Unit, Fondazione Cà Granda IRCCS Ospedale Maggiore Policlinico, Milan, Italy.
Abstract:
Cardiovascular disease risk has been consistently linked with particulate matter (PM) exposure. Cell-derived microvesicles (MVs) are released into plasma and transfer microRNAs (miRNAs) between tissues. MVs can be produced by the respiratory system in response to proinflammatory triggers, enter the circulatory system and remotely modify gene expression in cardiovascular tissues. However, whether PM affects MV signaling has never been investigated. In this study, we evaluated expression of microRNAs contained within plasma MVs upon PM exposure both in vivo and in vitro. In the in vivo study, we isolated plasma MVs from healthy steel plant workers before and after workplace PM exposure. We measured the expression of 88 MV-associated miRNAs by real-time polymerase chain reaction. To assess a possible source of the MV miRNAs identified in vivo, we measured their miRNA expression in PM-treated A549 pulmonary cell lines in vitro. MiRNA profiling of plasma MVs showed 5.62- and 13.95-fold increased expression of miR-128 and miR-302c, respectively, after 3 days of workplace PM exposure (P < 0.001). According to Ingenuity Pathway Analysis, miR-128 is part of coronary artery disease pathways, and miR-302c is part of coronary artery disease, cardiac hypertrophy and heart failure pathways. In vitro experiments confirmed a dose-dependent expression of miR-128 in MVs released from A549 cells after 6 h of PM treatment (P = 0.030). MiR-302c was expressed neither from A549 cells nor in reference lung RNA. These results suggest novel PM-activated molecular mechanisms that may mediate the effects of air pollution and could lead to the identification of new diagnostic and therapeutic interventions.
Insights
Particulate matter (PM) exposure increases specific microRNAs (miRNAs) in plasma microvesicles (MVs), potentially linking air pollution to cardiovascular disease. This study identifies novel PM-activated molecular pathways for diagnostics and therapeutics.
Area of Science:
- Environmental Health
- Molecular Biology
- Cardiovascular Research
Background:
- Cardiovascular disease (CVD) risk is linked to particulate matter (PM) exposure.
- Cell-derived microvesicles (MVs) transfer microRNAs (miRNAs) and can be influenced by respiratory inflammation.
- The impact of PM on MV signaling in CVD remains unexplored.
Purpose of the Study:
- To investigate if PM exposure alters miRNA content within plasma MVs.
- To explore potential mechanisms linking PM, MVs, and cardiovascular health.
- To identify novel biomarkers and therapeutic targets for PM-induced cardiovascular effects.
Main Methods:
- In vivo study: Plasma MVs isolated from steel plant workers before and after PM exposure.
- In vitro study: A549 pulmonary cells treated with PM to assess MV miRNA release.
- miRNA profiling using real-time polymerase chain reaction and Ingenuity Pathway Analysis.
Main Results:
- Workplace PM exposure significantly increased plasma MV expression of miR-128 (5.62-fold) and miR-302c (13.95-fold).
- miR-128 and miR-302c are implicated in coronary artery disease, cardiac hypertrophy, and heart failure pathways.
- In vitro, PM treatment induced dose-dependent miR-128 release from A549 cells.
Conclusions:
- PM exposure alters plasma MV miRNA profiles, suggesting a novel mechanism for air pollution's cardiovascular effects.
- Upregulated miR-128 in MVs may contribute to PM-induced cardiovascular pathology.
- These findings offer potential for new diagnostic markers and therapeutic strategies for air pollution-related CVD.
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