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Tcf20 deficiency is associated with increased liver fibrogenesis and alterations in mitochondrial metabolism in mice and humans.

Authors :
Córdoba‐Jover, Bernat
Ribera, Jordi
Portolés, Irene
Lecue, Elena
Rodriguez‐Vita, Juan
Pérez‐Sisqués, Leticia
Mannara, Francesco
Solsona‐Vilarrasa, Estel
García‐Ruiz, Carmen
Fernández‐Checa, José C.
Casals, Gregori
Rodríguez‐Revenga, Laia
Álvarez‐Mora, María Isabel
Arteche‐López, Ana
Díaz de Bustamante, Aranzazu
Calvo, Rosa
Pujol, Anna
Azkargorta, Mikel
Elortza, Felix
Malagelada, Cristina
Source :
Liver International; Aug2023, Vol. 43 Issue 8, p1822-1836, 15p, 2 Color Photographs, 2 Black and White Photographs, 2 Charts, 2 Graphs
Publication Year :
2023

Abstract

Background & Aims: Transcription co‐activator factor 20 (TCF20) is a regulator of transcription factors involved in extracellular matrix remodelling. In addition, TCF20 genomic variants in humans have been associated with impaired intellectual disability. Therefore, we hypothesized that TCF20 has several functions beyond those described in neurogenesis, including the regulation of fibrogenesis. Methods: Tcf20 knock‐out (Tcf20−/−) and Tcf20 heterozygous mice were generated by homologous recombination. TCF20 gene genotyping and expression was assessed in patients with pathogenic variants in the TCF20 gene. Neural development was investigated by immufluorescense. Mitochondrial metabolic activity was evaluated with the Seahorse analyser. The proteome analysis was carried out by gas chromatography mass‐spectrometry. Results: Characterization of Tcf20−/− newborn mice showed impaired neural development and death after birth. In contrast, heterozygous mice were viable but showed higher CCl4‐induced liver fibrosis and a differential expression of genes involved in extracellular matrix homeostasis compared to wild‐type mice, along with abnormal behavioural patterns compatible with autism‐like phenotypes. Tcf20−/− embryonic livers and mouse embryonic fibroblast (MEF) cells revealed differential expression of structural proteins involved in the mitochondrial oxidative phosphorylation chain, increased rates of mitochondrial metabolic activity and alterations in metabolites of the citric acid cycle. These results parallel to those found in patients with TCF20 pathogenic variants, including alterations of the fibrosis scores (ELF and APRI) and the elevation of succinate concentration in plasma. Conclusions: We demonstrated a new role of Tcf20 in fibrogenesis and mitochondria metabolism in mice and showed the association of TCF20 deficiency with fibrosis and metabolic biomarkers in humans. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14783223
Volume :
43
Issue :
8
Database :
Complementary Index
Journal :
Liver International
Publication Type :
Academic Journal
Accession number :
164936612
Full Text :
https://doi.org/10.1111/liv.15640