Journal
CELLULAR AND MOLECULAR LIFE SCIENCES
Volume 79, Issue 9, Pages -Publisher
SPRINGER BASEL AG
DOI: 10.1007/s00018-022-04520-x
Keywords
Immunosuppression; Kynurenine; Lifespan; Longevity; RelB; Retrotransposon
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Funding
- University of Eastern Finland (UEF) including Kuopio University Hospital
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The antagonistic pleiotropy hypothesis explains the aging process by proposing that certain genes may have beneficial effects during development but deleterious properties in aging. The aryl hydrocarbon receptor (AhR) is involved in various age-related degenerative processes, as well as stem cell pluripotency, immune system regulation, and differentiation of peripheral tissues. However, AhR signaling can also promote cellular senescence, pathological processes, and disturb energy metabolism. The complex connections with major signaling pathways and epigenetic regulation play a crucial role in the antagonistic pleiotropy of AhR signaling.
The antagonistic pleiotropy hypothesis is a well-known evolutionary theory to explain the aging process. It proposes that while a particular gene may possess beneficial effects during development, it can exert deleterious properties in the aging process. The aryl hydrocarbon receptor (AhR) has a significant role during embryogenesis, but later in life, it promotes several age-related degenerative processes. For instance, AhR factor (i) controls the pluripotency of stem cells and the stemness of cancer stem cells, (ii) it enhances the differentiation of embryonal stem cells, especially AhR signaling modulates the differentiation of hematopoietic stem cells and progenitor cells, (iii) it also stimulates the differentiation of immunosuppressive Tregs, Bregs, and M2 macrophages, and finally, (iv) AhR signaling participates in the differentiation of many peripheral tissues. On the other hand, AhR signaling is involved in many processes promoting cellular senescence and pathological processes, e.g., osteoporosis, vascular dysfunction, and the age-related remodeling of the immune system. Moreover, it inhibits autophagy and aggravates extracellular matrix degeneration. AhR signaling also stimulates oxidative stress, promotes excessive sphingolipid synthesis, and disturbs energy metabolism by catabolizing NAD(+) degradation. The antagonistic pleiotropy of AhR signaling is based on the complex and diverse connections with major signaling pathways in a context-dependent manner. The major regulatory steps include, (i) a specific ligand-dependent activation, (ii) modulation of both genetic and non-genetic responses, (iii) a competition and crosstalk with several transcription factors, such as ARNT, HIF-1 alpha, E2F1, and NF-kappa B, and (iv) the epigenetic regulation of target genes with binding partners. Thus, not only mTOR signaling but also the AhR factor demonstrates antagonistic pleiotropy in the regulation of the aging process.
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