Innate Immunity Receptor TLR9 Drives Erythrocyte Cholesterol and Ferroprotin Accumulation in a Glutaminase-Independent Manner. Implications for Metabolic Associated Fatty Liver Disease

Erythrocyte TLR9 is upregulated in MAFLD patients and drives cholesterol and ferroportin-1 accumulation in a glutaminase-independent manner. Augmented erythrocyte TLR9 could participate in metabolic inflammation during MAFLD.

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Publication Details

Journal
MAEDICA – a Journal of Clinical Medicine
Published
2025-03-15
DOI
https://doi.org/10.26574/maedica.2025.20.2.220
Primary Topic
Liver Disease Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
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article

Innate Immunity Receptor TLR9 Drives Erythrocyte Cholesterol and Ferroprotin Accumulation in a Glutaminase-Independent Manner. Implications for Metabolic Associated Fatty Liver Disease

D. S. Vlachos, Konstantinos Anagnostopoulos, Konstantinos Mimidis, Charalampos Papadopoulos et al.
MAEDICA – a Journal of Clinical Medicine
Liver Disease Diagnosis and Treatment
article

Innate Immunity Receptor TLR9 Drives Erythrocyte Cholesterol and Ferroprotin Accumulation in a Glutaminase-Independent Manner. Implications for Metabolic Associated Fatty Liver Disease

D. S. Vlachos, Konstantinos Anagnostopoulos, Konstantinos Mimidis, Charalampos Papadopoulos, Zoi Kyriakou, Nikolaos Politis, Panagiotis Veniamis, Tentes Ioannis
article en

Abstract

Erythrocyte TLR9 is upregulated in MAFLD patients and drives cholesterol and ferroportin-1 accumulation in a glutaminase-independent manner. Augmented erythrocyte TLR9 could participate in metabolic inflammation during MAFLD.

MAEDICA – a Journal of Clinical MedicineVol. 20(2)
Democritus University of Thrace (GR)
Openalex Percentile: Top 68%
Liver Disease Diagnosis and Treatment
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