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PSD3 downregulation confers protection against fatty liver disease.


ABSTRACT: Fatty liver disease (FLD) is a growing health issue with burdening unmet clinical needs. FLD has a genetic component but, despite the common variants already identified, there is still a missing heritability component. Using a candidate gene approach, we identify a locus (rs71519934) at the Pleckstrin and Sec7 domain-containing 3 (PSD3) gene resulting in a leucine to threonine substitution at position 186 of the protein (L186T) that reduces susceptibility to the entire spectrum of FLD in individuals at risk. PSD3 downregulation by short interfering RNA reduces intracellular lipid content in primary human hepatocytes cultured in two and three dimensions, and in human and rodent hepatoma cells. Consistent with this, Psd3 downregulation by antisense oligonucleotides in vivo protects against FLD in mice fed a non-alcoholic steatohepatitis-inducing diet. Thus, translating these results to humans, PSD3 downregulation might be a future therapeutic option for treating FLD.

SUBMITTER: Mancina RM 

PROVIDER: S-EPMC8803605 | biostudies-literature | 2022 Jan

REPOSITORIES: biostudies-literature

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PSD3 downregulation confers protection against fatty liver disease.

Mancina Rosellina M RM   Sasidharan Kavitha K   Lindblom Anna A   Wei Ying Y   Ciociola Ester E   Jamialahmadi Oveis O   Pingitore Piero P   Andréasson Anne-Christine AC   Pellegrini Giovanni G   Baselli Guido G   Männistö Ville V   Pihlajamäki Jussi J   Kärjä Vesa V   Grimaudo Stefania S   Marini Ilaria I   Maggioni Marco M   Becattini Barbara B   Tavaglione Federica F   Dix Carly C   Castaldo Marie M   Klein Stephanie S   Perelis Mark M   Pattou Francois F   Thuillier Dorothée D   Raverdy Violeta V   Dongiovanni Paola P   Fracanzani Anna Ludovica AL   Stickel Felix F   Hampe Jochen J   Buch Stephan S   Luukkonen Panu K PK   Prati Daniele D   Yki-Järvinen Hannele H   Petta Salvatore S   Xing Chao C   Schafmayer Clemens C   Aigner Elmar E   Datz Christian C   Lee Richard G RG   Valenti Luca L   Lindén Daniel D   Romeo Stefano S  

Nature metabolism 20220131 1


Fatty liver disease (FLD) is a growing health issue with burdening unmet clinical needs. FLD has a genetic component but, despite the common variants already identified, there is still a missing heritability component. Using a candidate gene approach, we identify a locus (rs71519934) at the Pleckstrin and Sec7 domain-containing 3 (PSD3) gene resulting in a leucine to threonine substitution at position 186 of the protein (L186T) that reduces susceptibility to the entire spectrum of FLD in individ  ...[more]

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