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Home › Dataset Library › Circadian temporal profiling of MMH-D3 hepatocytes › Plugin Library › Tocris Bioscience

Dataset: Circadian temporal profiling of MMH-D3 hepatocytes

The circadian clock generates daily rhythms in mammalian liver processes, such as glucose and lipid homeostasis, xenobiotic metabolism,...

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The circadian clock generates daily rhythms in mammalian liver processes, such as glucose and lipid homeostasis, xenobiotic metabolism, and regeneration. The mechanisms governing these rhythms are not well understood, particularly the distinct contributions of the cell-autonomous clock and central pacemaker to rhythmic liver physiology. Through microarray expression profiling in MMH-D3 hepatocytes, we identified over 1,000 transcripts that exhibit circadian oscillations, demonstrating that many rhythms can be driven by the cell-autonomous clock and that MMH-D3 is a valid circadian model system. The genes represented by these circadian transcripts displayed both co-phasic and anti-phasic organization within a protein-protein interaction network, suggesting the existence of competition for binding sites or partners by genes of disparate transcriptional phases. Multiple pathways displayed enrichment in MMH-D3 circadian transcripts, including the polyamine synthesis module of the glutathione metabolic pathway. The polyamine synthesis module, which is highly associated with cell proliferation and whose products are required for initiation of liver regeneration, includes enzymes whose transcripts exhibit circadian oscillations, such as ornithine decarboxylase (Odc1) and spermidine synthase (Srm). Metabolic profiling revealed that the enzymatic product of SRM, spermidine, cycles as well. Thus, the cell-autonomous hepatocyte clock can drive a significant amount of transcriptional rhythms and orchestrate physiologically relevant modules such as polyamine synthesis. Samples were collected every 2 hours for a duration of 46 hours from differentiated MMH-D3 hepatocytes synchronized via serum shock. Cells were synchronized by serum shock and incubated for 12 hours, and then samples were collected every 2 hours from 12 hours post-serum shock to 58 hours post-serum shock, for a total of 24 samples.

Species:
mouse

Samples:
24

Source:
E-GEOD-31049

PubMed:
22042857

Updated:
Dec.12, 2014

Registered:
Nov.11, 2014


Factors: (via ArrayExpress)
Sample TIME (HOURS) POST-SYNCHRONIZATION
GSM76919 12
GSM769192 14
GSM769193 16
GSM769194 18
GSM769195 20
GSM769196 22
GSM769197 24
GSM769198 26
GSM769199 28
GSM769200 30
GSM76920 32
GSM769202 34
GSM769203 36
GSM769204 38
GSM769205 40
GSM769206 42
GSM769207 44
GSM769208 46
GSM769209 48
GSM769210 50
GSM7692 52
GSM769212 54
GSM769213 56
GSM769214 58

Tags

  • cell
  • central
  • glucose
  • hepatocyte
  • lipid
  • liver
  • protein
  • serum

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