Summary: A new study reports human fat cells have their own internal clocks and circadian rhythms which affect metabolic functions.
Source: University of Surrey.
Fat cells in the human body have their own internal clocks and exhibit circadian rhythms affecting critical metabolic functions, new research in the journal Scientific Reports, finds.
Researchers led by Dr Jonathan Johnston from the University of Surrey conducted the first ever analysis of circadian rhythms in human fat taken from people isolated from daily environmental changes. Circadian rhythms are approximately 24-hour changes governed by the body’s internal clocks. Misalignment of ‘human clocks’ with each other and the environment is believed to be a major contributor to obesity and poor health.
During this unique study seven participants underwent regulated sleep-wake cycles and meal times before entering the laboratory, where they maintained this routine for a further three days.
Participants then experienced a 37- hour ‘constant routine’ during which time they did not experience daily changes in light-dark, feed-fast and sleep-wake cycles. Biopsies of fat tissue were taken at six hourly intervals and then followed by an analysis of gene expression.
Researchers identified 727 genes in the fat tissue that express their own circadian rhythm, many carrying out key metabolic functions. A clear separation in gene rhythms was identified with approximately a third peaking in the morning and two thirds in the evening.
Morning-peaking transcripts were associated with regulation of gene expression and nucleic acid biology (vital for cell functioning), while evening-peaking transcripts associated with redox activity and organic acid metabolism.
These rhythms, which are independent of external factors such as light and feeding, demonstrate that genes within fat cells naturally complete their functions at different times during the day which could impact on metabolic processes.
Fat cells play an important role in our body, acting as energy stores and controlling metabolism and appetite via hormone secretion.
Lead author Dr Jonathan Johnston, Reader in Chronobiology and Integrative Physiology, at the University of Surrey, said: “Tissues made up of fat cells don’t just store excess energy, they are active metabolic tissues, full of their own rhythms.
“This is the first time that we have been able to identify such rhythms in human fat. This provides us with more information about how human metabolism changes across the day and possibly why the body processes foods differently during day and night.”
About this neuroscience research article
Source: Natasha Meredith – University of Surrey Publisher: Organized by NeuroscienceNews.com. Image Source: NeuroscienceNews.com image is adapted from the University of Surrey news release. Original Research: Open access research for “Circadian regulation in human white adipose tissue revealed by transcriptome and metabolic network analysis” by Skevoulla Christou, Sophie M. T. Wehrens, Cheryl Isherwood, Carla S. Möller-Levet, Huihai Wu, Victoria L. Revell, Giselda Bucca, Debra J. Skene, Emma E. Laing, Simon N. Archer & Jonathan D. Johnston in Scientific Reports. Published February 6 2019. doi:10.1038/s41598-019-39668-3
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[cbtabs][cbtab title=”MLA”]University of Surrey “Fat Cells Work Different ‘Shifts’ Throughout the Day.” NeuroscienceNews. NeuroscienceNews, 25 February 2019. <https://neurosciencenews.com/fat-cell-shifts-10813/>.[/cbtab][cbtab title=”APA”]University of Surrey (2019, February 25). Fat Cells Work Different ‘Shifts’ Throughout the Day. NeuroscienceNews. Retrieved February 25, 2019 from https://neurosciencenews.com/fat-cell-shifts-10813/[/cbtab][cbtab title=”Chicago”]University of Surrey “Fat Cells Work Different ‘Shifts’ Throughout the Day.” https://neurosciencenews.com/fat-cell-shifts-10813/ (accessed February 25, 2019).[/cbtab][/cbtabs]
Circadian regulation in human white adipose tissue revealed by transcriptome and metabolic network analysis
Studying circadian rhythms in most human tissues is hampered by difficulty in collecting serial samples. Here we reveal circadian rhythms in the transcriptome and metabolic pathways of human white adipose tissue. Subcutaneous adipose tissue was taken from seven healthy males under highly controlled ‘constant routine’ conditions. Five biopsies per participant were taken at six-hourly intervals for microarray analysis and in silico integrative metabolic modelling. We identified 837 transcripts exhibiting circadian expression profiles (2% of 41619 transcript targeting probes on the array), with clear separation of transcripts peaking in the morning (258 probes) and evening (579 probes). There was only partial overlap of our rhythmic transcripts with published animal adipose and human blood transcriptome data. Morning-peaking transcripts associated with regulation of gene expression, nitrogen compound metabolism, and nucleic acid biology; evening-peaking transcripts associated with organic acid metabolism, cofactor metabolism and redox activity. In silico pathway analysis further indicated circadian regulation of lipid and nucleic acid metabolism; it also predicted circadian variation in key metabolic pathways such as the citric acid cycle and branched chain amino acid degradation. In summary, in vivo circadian rhythms exist in multiple adipose metabolic pathways, including those involved in lipid metabolism, and core aspects of cellular biochemistry.