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. 2020 May 29;432(12):3700–3713. doi: 10.1016/j.jmb.2019.12.044

Table 2.

Clock and circadian phenotypes upon modulation of the immune system.

Immune stimulus Effect Tissue/cells Reference
LPS Delays in circadian activity [77,78]
Disrupted clock gene expression:
  • -

    Reduced Dbp and Per2

SCN [76]
  • -

    Increased Per1

PVN [64]
  • -

    Per2 phase shift, reduced Bmal1

Macrophages [57]
  • -

    Reduced Per1 and Per2

Heart, liver [85]
  • -

    Altered Dbp, Ppara, Fkbp51

Liver [76]
  • -

    Reduced Per2

Ovaries [86]
  • -

    Disrupted rhythms and new rhythms

Lung [87]
  • -

    Reduced Bmal1

Macrophages [44]
TNFα Reduced LMA, prolonged rest phase [75]
Altered spiking activity SCN [80]
Reduced Dbp SCN [75]
Reduced Per1-3, Dbp, Tef, Hlf Fibroblasts [75]
Increased CRY1, reduced Dbp, Per2 Hepatocytes/liver [81]
IFNγ Altered spiking activity SCN [80]
Reduced Per1 SCN [80]
IFNα Reduced BMAL1 and CLOCK Hepatocytes/liver [82]
Salmonella Reduced Per2 Macrophages [56]
[79]
Turpentine oil Reduced Per1 and Per2 peaks Liver [93]
Shifted Per2 oscillation Heart