Tricyclic antidepressants target FKBP51 SUMOylation to restore glucocorticoid receptor activity

• Published in: Molecular psychiatry Vol. 27; no. 5; pp. 2533 - 2545
• Main Authors: Budziñski, Maia L., Sokn, Clara, Gobbini, Romina, Ugo, Belén, Antunica-Noguerol, María, Senin, Sergio, Bajaj, Thomas, Gassen, Nils C., Rein, Theo, Schmidt, Mathias V., Binder, Elisabeth B., Arzt, Eduardo, Liberman, Ana C.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.05.2022; Nature Publishing Group
• Subjects: 13/109; 13/95; 38/77; 42/89; 631/337; 631/378; 631/45; 631/80; 82/83; 96/106; Animals; Antidepressants; Antidepressive Agents, Tricyclic - pharmacology; Astrocytes; Behavioral Sciences; Biological Psychology; Clomipramine; Gene Expression Regulation; Glucocorticoids; Hsp90 protein; Medicine; Medicine & Public Health; Mice; Neurosciences; Pharmacotherapy; Psychiatry; Rats; Receptors, Glucocorticoid - metabolism; Repressors; SUMO protein; Sumoylation; Tacrolimus Binding Proteins - metabolism; Tricyclic antidepressants
• ISSN: 1359-4184; 1476-5578
• DOI: 10.1038/s41380-022-01491-0

FKBP51 is an important inhibitor of the glucocorticoid receptor (GR) signaling. High FKBP51 levels are associated to stress-related disorders, which are linked to GR resistance. SUMO conjugation to FKBP51 is necessary for FKBP51’s inhibitory action on GR. The GR/FKBP51 pathway is target of antidepressant action. Thus we investigated if these drugs could inhibit FKBP51 SUMOylation and therefore restore GR activity. Screening cells using Ni 2+ affinity and in vitro SUMOylation assays revealed that tricyclic antidepressants- particularly clomipramine- inhibited FKBP51 SUMOylation. Our data show that clomipramine binds to FKBP51 inhibiting its interaction with PIAS4 and therefore hindering its SUMOylation. The inhibition of FKBP51 SUMOylation decreased its binding to Hsp90 and GR facilitating FKBP52 recruitment, and enhancing GR activity. Reduction of PIAS4 expression in rat primary astrocytes impaired FKBP51 interaction with GR, while clomipramine could no longer exert its inhibitory action. This mechanism was verified in vivo in mice treated with clomipramine. These results describe the action of antidepressants as repressors of FKBP51 SUMOylation as a molecular switch for restoring GR sensitivity, thereby providing new potential routes of antidepressant intervention.