Department of Molecular Microbiology, Research Institute for Microbial Diseases (RIMD), Osaka University, Suita 565-0871, Japan.
Department of Molecular Microbiology, Research Institute for Microbial Diseases (RIMD), Osaka University, Suita 565-0871, Japan; Immunology Frontier Research Center, Osaka University, Suita 565-0871, Japan; Center for Infectious Diseases Education and Research, Osaka University, Suita 565-0871, Japan.
Trends Cell Biol. 2024 Aug;34(8):626-635. doi: 10.1016/j.tcb.2023.12.004. Epub 2024 Jan 13.
Two phenomena, the accumulation of senescent cells and changes in the gut microbiota, are thought to contribute to the decline of biological functions and the development of diseases associated with aging. However, the relationship between these two phenomena and their effects on aging remains to be clarified. Recently, we have reported that gut bacteria induce cellular senescence in ileal germinal center (GC) B cells, resulting in decreased IgA production and diversity. This, in turn, leads to an imbalance in the gut microbiota. Thus, the crosstalk between the gut microbiota and cellular senescence via the host immune system may establish a vicious cycle and contribute to the disruption of gut homeostasis associated with aging.
两种现象,衰老细胞的积累和肠道微生物组的变化,被认为是导致生物功能下降和与衰老相关疾病发展的原因。然而,这两种现象之间的关系及其对衰老的影响仍有待阐明。最近,我们报道了肠道细菌诱导回肠生发中心(GC)B 细胞发生细胞衰老,导致 IgA 产生和多样性减少。这反过来又导致肠道微生物组失衡。因此,肠道微生物组和通过宿主免疫系统的细胞衰老之间的串扰可能建立一个恶性循环,并导致与衰老相关的肠道内稳态的破坏。