Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Tokyo, Japan.
Division of Pathology, Department of Oral Diagnostic Sciences, School of Dentistry, Showa University, Tokyo, Japan; Department of Oral and Maxillofacial Surgery, School of Dentistry, Showa University, Tokyo, Japan.
Exp Cell Res. 2021 Dec 1;409(1):112889. doi: 10.1016/j.yexcr.2021.112889. Epub 2021 Oct 19.
Although stem cell aging leads to a decline in tissue homeostasis and regenerative capacity, it remains unclear whether salivary gland stem cell function changes during this process. However, the salivary glands are gradually replaced by connective tissue during aging. Here, we show a decline in the stem cell ability of CD133-positive stem/progenitor cells in the salivary glands of aged mice. The CD133-positive cells were isolated from young, adult, and aged mice. The number of CD133-positive cells was significantly decreased in aged mice. They also showed a lower sphere formation capacity compared to young and adult mice. RNA sequencing revealed that CD133-positive cells in aged mice exhibited lower gene expression of several aging-related genes, including FoxO3a, than those in young and adult mice. Salivary gland cells infected with a recombinant lentivirus encoding the FoxO3a gene showed a reduction in oxidative stress induced by hydrogen peroxide compared with those infected with a control virus. Thus, FoxO3a may inhibit stem cell aging via oxidative stress.
虽然干细胞衰老导致组织内稳态和再生能力下降,但尚不清楚唾液腺干细胞功能是否在此过程中发生变化。然而,随着衰老的进行,唾液腺逐渐被结缔组织取代。在这里,我们发现老年小鼠唾液腺中 CD133 阳性干细胞/祖细胞的干细胞能力下降。从年轻、成年和老年小鼠中分离出 CD133 阳性细胞。与年轻和成年小鼠相比,老年小鼠中 CD133 阳性细胞的数量明显减少。它们的球体形成能力也低于年轻和成年小鼠。RNA 测序显示,与年轻和成年小鼠相比,老年小鼠 CD133 阳性细胞中几种与衰老相关的基因(包括 FoxO3a)的表达水平较低。与感染对照病毒的细胞相比,感染携带 FoxO3a 基因的重组慢病毒的唾液腺细胞中由过氧化氢诱导的氧化应激减少。因此,FoxO3a 可能通过氧化应激抑制干细胞衰老。