Microplastics detected in cirrhotic liver tissue.


Journal

EBioMedicine
ISSN: 2352-3964
Titre abrégé: EBioMedicine
Pays: Netherlands
ID NLM: 101647039

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 09 04 2022
revised: 22 06 2022
accepted: 22 06 2022
pubmed: 15 7 2022
medline: 17 8 2022
entrez: 14 7 2022
Statut: ppublish

Résumé

The contamination of ecosystem compartments by microplastics (MPs) is an ubiquitous problem. MPs have been observed in mice tissues, and recently in human blood, stool and placenta. However, two aspects remain unclear: whether MPs accumulate in peripheral organs, specifically in the liver, and if liver cirrhosis favours this process. We aimed to examine human liver tissue samples to determine whether MPs accumulate in the liver. This proof-of-concept case series, conducted in Germany, Europe, analyzed tissue samples of 6 patients with liver cirrhosis and 5 individuals without underlying liver disease. A total of 17 samples (11 liver, 3 kidney and 3 spleen samples) were analyzed according to the final protocol. A reliable method for detection of MP particles from 4 to 30 µm in human tissue was developed. Chemical digestion of tissue samples, staining with Nile red, subsequent fluorescent microscopy and Raman spectroscopy were performed. Morphology, size and composition of MP polymers were assessed. Considering the limit of detection, all liver, kidney and spleen samples from patients without underlying liver disease tested negative for MPs. In contrast, MP concentrations in cirrhotic liver tissues tested positive and showed significantly higher concentrations compared to liver samples of individuals without underlying liver disease. Six different microplastic polymers ranging from 4 to 30 µm in size were detected. This proof-of-concept case series assessed the presence of MPs in human liver tissue and found six different MP polymers in the liver of individuals with liver cirrhosis, but not in those without underlying liver disease. Future studies are needed to evaluate whether hepatic MP accumulation represents a potential cause in the pathogenesis of fibrosis, or a consequence of cirrhosis and portal hypertension. No funding was received for conducting this investigator driven study.

Sections du résumé

BACKGROUND BACKGROUND
The contamination of ecosystem compartments by microplastics (MPs) is an ubiquitous problem. MPs have been observed in mice tissues, and recently in human blood, stool and placenta. However, two aspects remain unclear: whether MPs accumulate in peripheral organs, specifically in the liver, and if liver cirrhosis favours this process. We aimed to examine human liver tissue samples to determine whether MPs accumulate in the liver.
METHODS METHODS
This proof-of-concept case series, conducted in Germany, Europe, analyzed tissue samples of 6 patients with liver cirrhosis and 5 individuals without underlying liver disease. A total of 17 samples (11 liver, 3 kidney and 3 spleen samples) were analyzed according to the final protocol. A reliable method for detection of MP particles from 4 to 30 µm in human tissue was developed. Chemical digestion of tissue samples, staining with Nile red, subsequent fluorescent microscopy and Raman spectroscopy were performed. Morphology, size and composition of MP polymers were assessed.
FINDINGS RESULTS
Considering the limit of detection, all liver, kidney and spleen samples from patients without underlying liver disease tested negative for MPs. In contrast, MP concentrations in cirrhotic liver tissues tested positive and showed significantly higher concentrations compared to liver samples of individuals without underlying liver disease. Six different microplastic polymers ranging from 4 to 30 µm in size were detected.
INTERPRETATION CONCLUSIONS
This proof-of-concept case series assessed the presence of MPs in human liver tissue and found six different MP polymers in the liver of individuals with liver cirrhosis, but not in those without underlying liver disease. Future studies are needed to evaluate whether hepatic MP accumulation represents a potential cause in the pathogenesis of fibrosis, or a consequence of cirrhosis and portal hypertension.
FUNDING BACKGROUND
No funding was received for conducting this investigator driven study.

Identifiants

pubmed: 35835713
pii: S2352-3964(22)00328-0
doi: 10.1016/j.ebiom.2022.104147
pmc: PMC9386716
pii:
doi:

Substances chimiques

Microplastics 0
Plastics 0
Polymers 0
Water Pollutants, Chemical 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104147

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests All authors declare that they have no conflict of interests regarding this manuscript.

Références

Toxicol Appl Pharmacol. 2001 Sep 15;175(3):191-9
pubmed: 11559017
Environ Int. 2020 Mar;136:105411
pubmed: 31889555
Chemosphere. 2022 Mar;291(Pt 1):132714
pubmed: 34743871
World J Hepatol. 2015 Mar 27;7(3):304-14
pubmed: 25848460
Anal Chem. 2020 Feb 4;92(3):2443-2451
pubmed: 31939281
Gut. 2019 Aug;68(8):1516-1526
pubmed: 31076401
Mar Pollut Bull. 2017 Sep 15;122(1-2):403-408
pubmed: 28689849
Environ Sci Technol. 2017 Jun 20;51(12):6634-6647
pubmed: 28531345
Int J Environ Res Public Health. 2020 Feb 26;17(5):
pubmed: 32111046
Sci Total Environ. 2021 Feb 1;754:141948
pubmed: 32916488
Sci Total Environ. 2019 Oct 1;685:96-103
pubmed: 31174127
Int J Environ Res Public Health. 2020 Feb 13;17(4):
pubmed: 32069998
Clin Biochem Rev. 2008 Aug;29 Suppl 1:S49-52
pubmed: 18852857
Gut. 1970 Jun;11(6):466-70
pubmed: 5430371
Water Res. 2019 May 15;155:410-422
pubmed: 30861380
Environ Int. 2021 Jan;146:106274
pubmed: 33395930
J Autoimmun. 2010 May;34(3):J226-33
pubmed: 20096538
Sci Rep. 2017 Apr 24;7:46687
pubmed: 28436478
Sci Total Environ. 2021 May 1;767:144345
pubmed: 33434834
J Control Release. 2013 Jan 28;165(2):139-45
pubmed: 23127508
Environ Health Perspect. 1997 Sep;105 Suppl 5:1261-3
pubmed: 9400735
Ann N Y Acad Sci. 1975 Jan 31;246:164-71
pubmed: 1054950
Cytokine. 2020 Dec;136:155250
pubmed: 32882667
Mar Pollut Bull. 2015 Aug 15;97(1-2):5-12
pubmed: 26072046
Environ Sci Technol. 2021 Apr 20;55(8):5084-5096
pubmed: 33724830
Sci Total Environ. 2020 Mar 10;707:135578
pubmed: 31784176
Foods. 2020 Jan 09;9(1):
pubmed: 31936455
Sci Total Environ. 2020 Feb 1;702:134455
pubmed: 31733547
Ann Intern Med. 2019 Oct 1;171(7):453-457
pubmed: 31476765
Science. 2021 Feb 12;371(6530):672-674
pubmed: 33574197
Arch Toxicol. 2019 Jul;93(7):1817-1833
pubmed: 31139862
Environ Sci Pollut Res Int. 2018 Dec;25(36):36046-36063
pubmed: 30382517
Sci Total Environ. 2021 Feb 25;757:143872
pubmed: 33310568
Arch Toxicol. 2019 Jan;93(1):217-218
pubmed: 30604141
Front Immunol. 2018 Nov 27;9:2733
pubmed: 30538701
Environ Int. 2022 May;163:107199
pubmed: 35367073
Arch Toxicol. 2019 Jan;93(1):213-215
pubmed: 30604140
JGH Open. 2020 Nov 21;5(1):116-121
pubmed: 33490620
Environ Sci Technol. 2020 Apr 7;54(7):3740-3751
pubmed: 32119774
Environ Anal Health Toxicol. 2021 Mar;36(1):e2021004-0
pubmed: 33730791
Sci Total Environ. 2018 Aug 1;631-632:449-458
pubmed: 29529433
Sci Rep. 2017 Jan 24;7:41323
pubmed: 28117374
Environ Pollut. 2020 Oct;265(Pt A):115025
pubmed: 32806417
Toxicology. 2021 Feb 15;449:152665
pubmed: 33359712
Sci Rep. 2016 Jul 14;6:29516
pubmed: 27412365
Adv Drug Deliv Rev. 2001 Aug 23;50(1-2):107-42
pubmed: 11489336
Clin Liver Dis (Hoboken). 2021 Jun 04;17(5):365-370
pubmed: 34136143
Biochim Biophys Acta. 2015 Oct;1853(10 Pt A):2411-9
pubmed: 26164626
Glob Chang Biol. 2018 Apr;24(4):1405-1416
pubmed: 29245177
Pharmaceutics. 2021 Jun 22;13(7):
pubmed: 34206212
Prog Histochem Cytochem. 2012 Jan;46(4):185-252
pubmed: 22240063

Auteurs

Thomas Horvatits (T)

I. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: t.horvatits@uke.de.

Matthias Tamminga (M)

Center for Earth System Research and Sustainability (CEN), University of Hamburg, Hamburg, Germany.

Beibei Liu (B)

I. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Marcial Sebode (M)

I. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Antonella Carambia (A)

I. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Lutz Fischer (L)

Department of Transplant Surgery, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Klaus Püschel (K)

Institute of Legal Medicine, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Samuel Huber (S)

I. Department of Medicine, Gastroenterology and Hepatology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Elke Kerstin Fischer (EK)

Center for Earth System Research and Sustainability (CEN), University of Hamburg, Hamburg, Germany. Electronic address: elke.fischer@uni-hamburg.de.

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