Morphostructural Analysis of PAH-Rich Human Adipose Tissue: A Potential Silent Sequestration Site

Read full text
Authors: Elena Stocco, Silvia Barbon, Martina Contran, Valentina Manzo, Daniele Brunelli, Luca Sorarù, Alice Franchin, Elena Gregoris, Marco Roman, Andrea Gambaro, Warren R. L. Cairns, Raffaele De
+3 more Vincenzo Vindigni, Veronica Macchi, Andrea Porzionato
Cited by: 1
References: 59

Abstract

Polycyclic aromatic hydrocarbons (PAHs) are widespread, persistent pollutants that can be sequestered within human adipose tissue due to their lipophilic nature. While this accumulation poses toxicological risks depending on dose and individual susceptibility, the specific morphological impact of chronic PAH storage on tissue architecture remains poorly defined. Here, we performed a histopathological and morphometric analysis on human subcutaneous adipose tissue samples characterized by high pyrene levels. We evaluated tissue organization, collagen distribution, the presence of inflammatory, neural, and vascular alterations and adipocyte morphometry to assess the structural response to PAH sequestration. Despite high pyrene concentrations, PAH-positive tissues maintained preserved overall architecture with normal collagen distribution, absence of lymphocytic infiltration, low macrophages, unaltered nerve fiber patterns, without evidence of vascular remodeling. Morphometry revealed smaller adipocyte area in PAH-positive samples, although not statistically significant. Our experimental data indicate that high PAH accumulation does not necessarily induce subcutaneous adipose tissue remodeling, suggesting that biochemical or metabolic alterations might occur even in the absence of evident histological changes. Further studies, with a broadened cohort, are needed to define the threshold at which PAHs' presence translates into permanent tissue damage.

Fields of Study & Subjects

Toxic Organic Pollutants Impact Adipokines Inflammation and Metabolic Diseases Effects and risks of endocrine disrupting chemicals

Publication details

Journal / source
International Journal of Molecular Sciences
Publisher
MDPI AG
Volume
27
Issue
12
Pages
5607–5607
Publication date
21 June 2026
Language
EN