Increased hyaluronan by naked mole-rat Has2 improves healthspan in mice

Abundant high-molecular-mass hyaluronic acid (HMM-HA) contributes to cancer resistance and possibly to the longevity of the longest-lived rodent-the naked mole-rat1,2. To study whether the benefits of HMM-HA could be transferred to other animal species, we generated a transgenic mouse overexpressing naked mole-rat hyaluronic acid synthase 2 gene (nmrHas2). nmrHas2 mice showed an increase in hyaluronan levels in several tissues, and a lower incidence of spontaneous and induced cancer, extended lifespan and improved healthspan. The transcriptome signature of nmrHas2 mice shifted towards that of longer-lived species. The most notable change observed in nmrHas2 mice was attenuated inflammation across multiple tissues. HMM-HA reduced inflammation through several pathways, including a direct immunoregulatory effect on immune cells, protection from oxidative stress and improved gut barrier function during ageing. These beneficial effects were conferred by HMM-HA and were not specific to the nmrHas2 gene. These findings demonstrate that the longevity mechanism that evolved in the naked mole-rat can be exported to other species, and open new paths for using HMM-HA to improve lifespan and healthspan.

Automated summary

Abundant high-molecular-mass hyaluronic acid (HMM-HA) contributes to cancer resistance and longevity in naked mole-rats. A study showed that overexpressing the naked mole-rat hyaluronic acid synthase 2 gene (nmrHas2) in mice resulted in increased hyaluronan levels, reduced incidence of cancer, extended lifespan, and improved healthspan. The beneficial effects were mediated by HMM-HA and not specific to the nmrHas2 gene, suggesting that the longevity mechanism observed in naked mole-rats can be transferred to other species.