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Updated: Apr 17, 2026

In vivo Liver Endocytosis Followed by Purification of Liver Cells by Liver Perfusion
Published on: November 10, 2011
Enolase is regulated by Liver X Receptors
Hugues De Boussac1, Salwan Maqdasy2, Amalia Trousson1
1Université Clermont Auvergne, Université Blaise Pascal, Génétique Reproduction et Développement, BP 10448, F63000 Clermont-Ferrand, France; CNRS, UMR 6293, GReD, F-63177 Aubiere, France; INSERM, UMR 1103, GReD, F-63177 Aubiere, France; Centre de Recherche en Nutrition Humaine d'Auvergne, F-63000 Clermont-Ferrand, France.
Abstract:
Enolase is a glycolytic enzyme known to inhibit cholesteryl ester hydrolases (CEHs). Cholesteryl ester loading of macrophages, as occurs during atherosclerosis, is accompanied by increased Enolase protein and activity. Here, we describe that J774 macrophages treated with LXR agonists exhibit reduced Enolase transcript and protein abundance. Moreover, we show that this reduction is further potentiated by activation of the LXR/RXR heterodimer with the RXR ligand 9-cis retinoic acid. Enolase levels are also reduced in vivo following activation of LXRs in the intestine, but not in the liver. This effect is lost in Lxrαβ-/- mice. In aggregate, our study identified Enolase as a new target of LXRs in vivo, which may promote cholesterol mobilization for subsequent efflux.
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