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The interplay between mast cells, pineal gland, and circadian rhythm: Links between histamine, melatonin, and inflammatory mediators

期刊

JOURNAL OF PINEAL RESEARCH
卷 70, 期 2, 页码 -

出版社

WILEY
DOI: 10.1111/jpi.12699

关键词

circadian rhythm; clock genes; histamine; inflammation; mast cells; melatonin

资金

  1. Hickam Endowed Chair, Gastroenterology, Medicine, Indiana University
  2. PSC Partners Seeking a Cure
  3. SRCS Award
  4. RCS from the United States Department of Veterans Affairs, Biomedical Laboratory Research and Development Service [1I01BX003031]
  5. RCS VA Merit Award from the United States Department of Veterans Affairs, Biomedical Laboratory Research and Development Service [1I01BX003031]
  6. NIH [DK108959, DK119421, DK115184, DK076898]
  7. Strategic Research Initiative, Indiana University

向作者/读者索取更多资源

The daily rhythmicity in our body is controlled by a circadian clock in the suprachiasmatic nucleus in the hypothalamus. Mast cells play a protective role against pathogens and inflammation and are associated with the circadian rhythm. Melatonin and histamine modulate circadian rhythms by regulating NF-kappa B, offering a promising therapeutic strategy for MC-mediated inflammatory diseases.
Our daily rhythmicity is controlled by a circadian clock with a specific set of genes located in the suprachiasmatic nucleus in the hypothalamus. Mast cells (MCs) are major effector cells that play a protective role against pathogens and inflammation. MC distribution and activation are associated with the circadian rhythm via two major pathways, IgE/Fc epsilon RI- and IL-33/ST2-mediated signaling. Furthermore, there is a robust oscillation between clock genes and MC-specific genes. Melatonin is a hormone derived from the amino acid tryptophan and is produced primarily in the pineal gland near the center of the brain, and histamine is a biologically active amine synthesized from the decarboxylation of the amino acid histidine by the L-histidine decarboxylase enzyme. Melatonin and histamine are previously reported to modulate circadian rhythms by pathways incorporating various modulators in which the nuclear factor-binding near the kappa light-chain gene in B cells, NF-kappa B, is the common key factor. NF-kappa B interacts with the core clock genes and disrupts the production of pro-inflammatory cytokine mediators such as IL-6, IL-13, and TNF-alpha. Currently, there has been no study evaluating the interdependence between melatonin and histamine with respect to circadian oscillations in MCs. Accumulating evidence suggests that restoring circadian rhythms in MCs by targeting melatonin and histamine via NF-kappa B may be promising therapeutic strategy for MC-mediated inflammatory diseases. This review summarizes recent findings for circadian-mediated MC functional roles and activation paradigms, as well as the therapeutic potentials of targeting circadian-mediated melatonin and histamine signaling in MC-dependent inflammatory diseases.

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