Time-of-day-dependent variation of the human liver transcriptome and metabolome is disrupted in MASLD
Manuel Johanns,
Joel T. Haas,
Violetta Raverdy,
Jimmy Vandel,
Julie Chevalier-Dubois,
Loic Guille,
Bruno Derudas,
Benjamin Legendre,
Robert Caiazzo,
Helene Verkindt,
Viviane Gnemmi,
Emmanuelle Leteurtre,
Mehdi Derhourhi,
Amélie Bonnefond,
Philippe Froguel,
Jérôme Eeckhoute,
Guillaume Lassailly,
Philippe Mathurin,
François Pattou,
Bart Staels,
Philippe Lefebvre
Affiliations
Manuel Johanns
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Joel T. Haas
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Violetta Raverdy
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1190-EGID, F-59000 Lille, France
Jimmy Vandel
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Julie Chevalier-Dubois
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Loic Guille
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Bruno Derudas
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Benjamin Legendre
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1190-EGID, F-59000 Lille, France
Robert Caiazzo
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1190-EGID, F-59000 Lille, France
Helene Verkindt
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1190-EGID, F-59000 Lille, France
Viviane Gnemmi
Univ. Lille, Inserm, CHU Lille, UMR 1172, Lille, France
Emmanuelle Leteurtre
Univ. Lille, Inserm, CHU Lille, UMR 1172, Lille, France
Mehdi Derhourhi
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR 1283/8199-EGID, F-59000 Lille, France
Amélie Bonnefond
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR 1283/8199-EGID, F-59000 Lille, France; Department of Metabolism, Imperial College London; London, United Kingdom
Philippe Froguel
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR 1283/8199-EGID, F-59000 Lille, France; Department of Metabolism, Imperial College London; London, United Kingdom
Jérôme Eeckhoute
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Guillaume Lassailly
Univ. Lille, Inserm, CHU Lille, UMR 995-LIRIC, Lille, France
Philippe Mathurin
Univ. Lille, Inserm, CHU Lille, UMR 995-LIRIC, Lille, France
François Pattou
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1190-EGID, F-59000 Lille, France
Bart Staels
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France
Philippe Lefebvre
Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, UMR1011-EGID, F-59000 Lille, France; Corresponding author. Address: Inserm UMR1011, Bldg J&K, Faculté de Médecine Henri Warembourg, Pôle Recherche, Blvd du Prof Leclerc, 59000, Lille, France; Tel.: +33.3.20974220.
Background & Aims: Liver homeostasis is ensured in part by time-of-day-dependent processes, many of them being paced by the molecular circadian clock. Liver functions are compromised in metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction-associated steatohepatitis (MASH), and clock disruption increases susceptibility to MASLD progression in rodent models. We therefore investigated whether the time-of-day-dependent transcriptome and metabolome are significantly altered in human steatotic and MASH livers. Methods: Liver biopsies, collected within an 8 h-window from a carefully phenotyped cohort of 290 patients and histologically diagnosed to be either normal, steatotic or MASH hepatic tissues, were analyzed by RNA sequencing and unbiased metabolomic approaches. Time-of-day-dependent gene expression patterns and metabolomes were identified and compared between histologically normal, steatotic and MASH livers. Results: Herein, we provide a first-of-its-kind report of a daytime-resolved human liver transcriptome-metabolome and associated alterations in MASLD. Transcriptomic analysis showed a robustness of core molecular clock components in steatotic and MASH livers. It also revealed stage-specific, time-of-day-dependent alterations of hundreds of transcripts involved in cell-to-cell communication, intracellular signaling and metabolism. Similarly, rhythmic amino acid and lipid metabolomes were affected in pathological livers. Both TNFα and PPARγ signaling were predicted as important contributors to altered rhythmicity. Conclusion: MASLD progression to MASH perturbs time-of-day-dependent processes in human livers, while the differential expression of core molecular clock components is maintained. Impact and implications: This work characterizes the rhythmic patterns of the transcriptome and metabolome in the human liver. Using a cohort of well-phenotyped patients (n = 290) for whom the time-of-day at biopsy collection was known, we show that time-of-day variations observed in histologically normal livers are gradually perturbed in liver steatosis and metabolic dysfunction-associated steatohepatitis. Importantly, these observations, albeit obtained across a restricted time window, provide further support for preclinical studies demonstrating alterations of rhythmic patterns in diseased livers. On a practical note, this study indicates the importance of considering time-of-day as a critical biological variable which may significantly affect data interpretation in animal and human studies of liver diseases.