# Micro- and Nanoplastics Exposure Across the Lifespan: One Health Implications for Aging and Longevity

**Authors:** Chantalle Moulton, Anna Baroni, Ennio Tasciotti

PMC · DOI: 10.3390/jox16020052 · 2026-03-19

## TL;DR

This paper reviews how micro- and nanoplastics may affect aging and health, suggesting they could worsen age-related diseases through biological mechanisms like inflammation and cellular damage.

## Contribution

The paper introduces a One Health perspective to explore how micro- and nanoplastics impact aging, linking environmental exposure to biological mechanisms and health outcomes in older adults.

## Key findings

- Micro- and nanoplastics trigger oxidative stress, inflammation, and cellular senescence, which are key drivers of aging.
- MNPs may contribute to age-related diseases by affecting cardiovascular, nervous, and immune systems.
- There is a need for more epidemiological studies to confirm the health risks of MNPs in aging populations.

## Abstract

Micro- and nanoplastics (MNPs) are pervasive environmental contaminants with growing relevance for human health across the lifespan. Older adults may be especially vulnerable to their effects due to cumulative lifetime exposure, age-related physiological changes, and a higher burden of chronic disease. Adopting a One Health perspective, this review synthesizes current evidence on the sources, exposure pathways, and biological effects of MNPs, integrating findings from environmental, animal, and human studies with a specific focus on aging populations. Experimental studies consistently show that MNP exposure triggers oxidative stress, inflammation, mitochondrial dysfunction, and cellular senescence, mechanisms central to biological aging. These processes are linked to dysfunction of the cardiovascular, nervous, gastrointestinal, and immune systems, suggesting that MNPs may contribute to the development or progression of age-related diseases. Within the One Health framework, MNPs also act as carriers of chemical additives and environmental pollutants, potentially amplifying health risks through combined and cumulative exposures along food chains and ecosystems. Despite increasing mechanistic evidence, direct epidemiological data in older adults remain limited. This review highlights key knowledge gaps and emphasizes the need for integrative, longitudinal research to clarify the role of MNPs in aging and to inform public health and environmental policy.

## Full-text entities

- **Genes:** IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Tlr4 (toll-like receptor 4) [NCBI Gene 21898] {aka Lps, Ly87, Ran/M1, Rasl2-8}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CAT (catalase) [NCBI Gene 847], SCARB1 (scavenger receptor class B member 1) [NCBI Gene 949] {aka CD36L1, CLA-1, CLA1, HDLCQ6, HDLQTL6, SR-BI}, GPX4 (glutathione peroxidase 4) [NCBI Gene 2879] {aka GPx-4, GSHPx-4, MCSP, PHGPx, SMDS, snGPx}, Yap1 (yes-associated protein 1) [NCBI Gene 22601] {aka Yap, Yap65, Yki, Yorkie}, PRKAB1 (protein kinase AMP-activated non-catalytic subunit beta 1) [NCBI Gene 5564] {aka AMPK, HAMPKb}, SLC7A11 (solute carrier family 7 member 11) [NCBI Gene 23657] {aka CCBR1, xCT}, DNM1L (dynamin 1 like) [NCBI Gene 10059] {aka DLP1, DRP1, DVLP, DYMPLE, EMPF, EMPF1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, Snca (synuclein, alpha) [NCBI Gene 20617] {aka NACP, alpha-Syn, alphaSYN}, FOSL1 (FOS like 1, AP-1 transcription factor subunit) [NCBI Gene 8061] {aka FRA, FRA1, fra-1}, OPA1 (OPA1 mitochondrial dynamin like GTPase) [NCBI Gene 4976] {aka BERHS, MGM1, MTDPS14, MTDPS14A, MTDPS14B, NPG}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, NLRP3 (NLR family pyrin domain containing 3) [NCBI Gene 114548] {aka AGTAVPRL, AII, AVP, C1orf7, CIAS1, CLR1.1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, ULK1 (unc-51 like autophagy activating kinase 1) [NCBI Gene 8408] {aka ATG1, ATG1A, UNC51, Unc51.1, hATG1}, MLKL (mixed lineage kinase domain like pseudokinase) [NCBI Gene 197259] {aka hMLKL}
- **Diseases:** cytotoxicity (MESH:D064420), immune dysfunction (MESH:D007154), infectious disease (MESH:D003141), immune dysregulation (OMIM:614878), cognitive decline (MESH:D003072), PD (MESH:D010300), frailty (MESH:D000073496), Mitochondrial Dysfunction (MESH:D028361), gastrointestinal, metabolic, and immune disturbances (MESH:D005767), immune and endocrine disruption (MESH:D004700), endothelial dysfunction (MESH:D014652), neurodegeneration (MESH:D019636), Inflammation (MESH:D007249), impaired reproduction (MESH:D060737), injury to (MESH:D014947), Metabolic Impairment (MESH:D008659), dementia (MESH:D003704), insulin resistance (MESH:D007333), chronic (MESH:D002908), zoonotic diseases (MESH:D015047), disease (MESH:D004194), MNP (MESH:C536681), age (MESH:D019588), DNA injury (MESH:D004266)
- **Chemicals:** polypropylene (MESH:D011126), MDA (MESH:D015104), ATP (MESH:D000255), PBS (MESH:C089797), PS (MESH:D010758), lipid (MESH:D008055), nitrogen (MESH:D009584), tryptophan (MESH:D014364), benzoic acid (MESH:D019817), calcium (MESH:D002118), polyethylene terephthalate (MESH:D011093), thymine (MESH:D013941), Micro (-), ROS (MESH:D017382), nitrate (MESH:D009566), Polymer (MESH:D011108), plastic (MESH:D010969), cordycepin (MESH:C058120), polystyrene (MESH:D011137), PCL (MESH:C016240), carbon (MESH:D002244), methionine (MESH:D008715), salt (MESH:D012492), TN (MESH:C009497), polyethylene (MESH:D020959), oxygen (MESH:D010100), malondialdehyde (MESH:D008315), PVC (MESH:D011143), heavy metals (MESH:D019216), GSH (MESH:D005978), PLA (MESH:C033616)
- **Species:** Homo sapiens (human, species) [taxon 9606], C. elegans [taxon 328850], Ostreidae (oysters, family) [taxon 6563], Mus musculus (house mouse, species) [taxon 10090], Myurella sp. NP (species) [taxon 1167538], Danio rerio (leopard danio, species) [taxon 7955]
- **Mutations:** A53T
- **Cell lines:** RPE — Homo sapiens (Human), Telomerase immortalized cell line (CVCL_4388)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13010698/full.md

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Source: https://tomesphere.com/paper/PMC13010698