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Petrus lab

The focus of our lab is to understand how disruptions of the circadian system, such as in shift work, leads to disease. We are particularly interested in metabolic and mental co-morbidity as we believe circadian malfunction is a common denominator linking these health problems.

The group is part of the Endocrinology Unit at the Department of Medicine, Huddinge (MedH).

Circadian rhythms

Like most other living organisms, humans have evolved to function in harmony with the day/night cycles. The biological processes following a  檀24-hour cycle are termed circadian (from the latin words Circa=about and Diem=day). Circadian rhythms are controlled by a genetically encoded 鈥渕olecular clock鈥 that exists in every nucleated cell and thus, in every organ. At its core, the molecular clock consists of a transcriptional-translational feedback loop regulating the rhythmic expression of thousands of genes. The clock in different tissues forms a network that communicates to align bodily functions with the time of day. Circadian disruption is caused by untimely light exposure, food intake and stress. Modern societies exist with artificial light at night, 24-hour access to hypercaloric foods and chronic stress.

Inter-organ communication

Our research focuses on understanding how environmental factors are integrated by the circadian system in specific organs and subsequently influencing rhythms in distant tissues. Circadian inter-organ communication involves several processes including metabolic signaling. The central clock is the main driver of systemic metabolic rhythms by controlling appetite and energy expenditure while the clocks in metabolically active organs, such as the liver and fat tissue, contribute to regulate metabolic rhythms by integrating nutritional cues.

Metabolic-epigenetic crosstalk

The circadian clock is tightly coupled with metabolism, as specific metabolites act as substrates and co-substrates for epigenetic regulators; factors changing the DNA structure without changing the sequence. Hence, circadian metabolic signaling from one organ can control rhythmic gene expression in a distant tissue. Thus, different tissue clocks cooperate to align behavioral and physiological rhythms to the time of day. Our project aims to delineate these mechanisms and how they relate to metabolic and mental health.

An overview of the research program

An illustrated photo of the human body.
An overview of the research program; we are interested in understanding how environmental factors impact on circadian inter-organ communication and the subsequent epigenetic programming. Photo: BioRender

Publications

Selected publications

  • Article: MOLECULAR METABOLISM. 2022;64:101556
    Petrus P; Cervantes M; Samad M; Sato T; Chao A; Sato S; Koronowski KB; Park G; Alam Y; Mejhert N; Seldin MM; Kuhm JMM; Dyar KA; Lutter D; Baldi P; Kaiser P; Jang C; Sassone-Corsi P
  • Article: CELL METABOLISM. 2020;31(2):375-390.e11
    Petrus P; Lecoutre S; Dollet L; Wiel C; Sulen A; Gao H; Tavira B; Laurencikiene J; Rooyackers O; Checa A; Douagi I; Wheelock CE; Arner P; McCarthy M; Bergo MO; Edgar L; Choudhury RP; Aouadi M; Krook A; Ryden M
  • Review: TRENDS IN ENDOCRINOLOGY AND METABOLISM. 2018;29(10):675-685
    Lecoutre S; Petrus P; Ryden M; Breton C
  • Article: JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM (JCEM). 2018;103(2):710-721
    Petrus P; Bialesova L; Checa A; Kerr A; Naz S; Backdahl J; Gracia A; Toft S; Dahlman-Wright K; Heden P; Dahlman I; Wheelock CE; Arner P; Mejhert N; Gao H; Ryden M

Funding

  • Novo Nordisk foundation
  • The Wenner-Gren foundations
  • 脜ke Wiberg foundation