team D. LANGIN / P. GOURDY
AdipoLive
Adipose tissue and liver metabolism in metabolic diseases
Adipose tissue and liver are organs that occupy a central role in lipid and glucose metabolism. Our laboratory investigates the roles of key enzymes such as neutral lipases in adipose tissue and their transcriptional control, notably through estrogen receptor a in the liver. Dysregulation of these metabolic pathways is investigated in metabolic diseases such as obesity, diabetes and metabolic dysfunction-associated steatotic liver disease (MASLD).
TEAM MEMBERS
ERC Synergy program spheres:
Lipid droplet hypertrophy: the link between adipocyte dysfunction and cardiometabolic diseases.
Coordinators : Dominique LANGIN, Mikael RYDEN (Karolinska Institute), Bruno Antonny (IPMC CNRS/UCA).
https://erc-spheres.univ-tlse3.fr/
metabolic roles of adipose lipases
Coordinators : Pierre-Damien DENECHAUD, Etienne MOUISEL, Dominique LANGIN.
Adipocyte lipases (ATGL and HSL) catalyze the hydrolysis of triacylglycerol stores releasing fatty acids into the bloodstream. Adipose tissue lipolysis is a catabolic pathway essential to maintain energy balance in physiological conditions. Its dysregulation is observed in metabolic disorders such as obesity, diabetes and MASLD. We investigate the impact of adipocyte lipase deficiency in white and brown adipose tissue metabolism and remodeling as well as the systemic consequences, notably on the pancreas and liver.
SEX differences in MASLD
Coordinators : Alexandra MONTAGNER, Pierre GOURDY.
Metabolic dysfunction-associated steatotic liver disease (MASLD) is sexually dimorphic, involving the protective actions of estrogens against its occurrence and progression towards the more severe stages in women. Our work aims to better understand the underlying molecular mechanisms, and more specifically the role of the estrogen receptor ERα in modulating the white adipose tissue to liver dialogue in physiological and pathological conditions.
SELECTED publications
ChREBPβ is dispensable for the control of glucose homeostasis and energy balance. Recazens E, Tavernier G, Dufau J, Bergoglio C, Benhamed F, Cassant-Sourdy S, Marques MA, Caspar-Bauguil S, Brion A, Monbrun L, Dentin R, Ferrier C, Leroux M, Denechaud PD, Moro C, Concordet JP, Postic C, Mouisel E, Langin D. JCI Insights. 2022. Pubmed
Metabolic and cardiovascular adaptations to an 8-wk lifestyle weight loss intervention in younger and older obese men. Vion J, Sramkova V, Montastier E, Marquès MA, Caspar-Bauguil S, Duparc T, Martinez LO, Bourlier V, Harant I, Larrouy D, Moussaoui N, Bonnel S, Vindis C, Dray C, Valet P, Saulnier-Blache JS, Schanstra JP, Thalamas C, Viguerie N, Moro C, Langin D. Am J Physiol Endocrinol Metab. 2021. Pubmed
Integrative study of diet-induced mouse models of NAFLD identifies PPARα as a sexually dimorphic drug target. Smati S, Polizzi A, Fougerat A, Ellero-Simatos S, Blum Y, Lippi Y, Régnier M, Laroyenne A, Huillet M, Arif M, Zhang C, Lasserre F, Marrot A, Al Saati T, Wan J, Sommer C, Naylies C, Batut A, Lukowicz C, Fougeray T, Tramunt B, Dubot P, Smith L, Bertrand-Michel J, Hennuyer N, Pradere JP, Staels B, Burcelin R, Lenfant F, Arnal JF, Levade T, Gamet-Payrastre L, Lagarrigue S, Loiseau N, Lotersztajn S, Postic C, Wahli W, Bureau C, Guillaume M, Mardinoglu A, Montagner A, Gourdy P, Guillou H. Gut. 2022. Pubmed
Selective Liver Estrogen Receptor α Modulation Prevents Steatosis, Diabetes, and Obesity Through the Anorectic Growth Differentiation Factor 15 Hepatokine in Mice. Guillaume M, Riant E, Fabre A, Raymond-Letron I, Buscato M, Davezac M, Tramunt B, Montagner A, Smati S, Zahreddine R, Palierne G, Valera MC, Guillou H, Lenfant F, Unsicker K, Metivier R, Fontaine C, Arnal JF, Gourdy P. Hepatol Commun. 2019. Pubmed
Interaction between hormone-sensitive lipase and ChREBP in fat cells controls insulin sensitivity.
FUNDINGS
Equipe Langin
Inserm/UPS UMR 1297 - I2MC Institut des Maladies Métaboliques et Cardiovasculaires
1 avenue Jean Poulhès - BP 84225 - 31432 Toulouse Cedex 4
Tél. : 05 61 32 56 00
Horaires
Du lundi au vendredi
8h30 - 12h30 / 13h45 -16h45