Immunosenescence is an age-dependent decline in immune functions and hallmark of aging in diverse species, ranging from invertebrates to mammals. However, identifying the factors responsible for immunosenescence is challenging because of the complexity of immune systems and aging in mammals. The roundworm Caenorhabditis elegans is suitable for understanding immunosenescence because of its simple immune system and rapid aging process. In this review, we discuss the advances in our understanding of immunosenescence in C. elegans. PMK-1/p38 mitogen-activated protein kinase (MAPK), SKN-1/NRF, and ZIP-10/bZIP transcription factor regulate immunosenescence through p38 MAPK and insulin/IGF-1 signaling pathways. Because these factors and pathways are evolutionarily conserved, the findings discussed in this review may help understand the mechanisms underlying immunosenescence and develop new treatment therapy for immunosenescence in humans.
机构:
Univ Massachusetts, Sch Med, Div Infect Dis & Immunol, Program Innate Immun, Worcester, MA 01605 USAUniv Massachusetts, Sch Med, Div Infect Dis & Immunol, Program Innate Immun, Worcester, MA 01605 USA
机构:
NYU, Ctr Genom & Syst Biol, New York, NY 10012 USA
NYU, Dept Biol, New York, NY 10012 USA
NYU, Abu Dhabi, U Arab EmiratesNYU, Ctr Genom & Syst Biol, New York, NY 10012 USA
Gunsalus, Kristin C.
Rhrissorrakrai, Kahn
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机构:
NYU, Ctr Genom & Syst Biol, New York, NY 10012 USA
NYU, Dept Biol, New York, NY 10012 USANYU, Ctr Genom & Syst Biol, New York, NY 10012 USA