4.5 Article

Klotho overexpression protects against renal aging along with suppression of transforming growth factor-β1 signaling pathways

Journal

AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
Volume 321, Issue 6, Pages F799-F811

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajprenal.00609.2020

Keywords

aging; cell cycle arrest; interstitial fibrosis; klotho; oxidative stress

Funding

  1. Tsuchiya Memorial Medical Foundation

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The study showed that klotho overexpression can improve certain aging features in the kidneys of aging mice, such as reducing kidney damage, lowering blood pressure, and decreasing oxidative stress levels. These findings suggest that klotho overexpression is beneficial for protecting the kidneys from age-related damage.
Klotho is an antiaging protein reported to suppress transforming growth factor-I31 (TGF-I31) signaling. Aging kidneys are characterized by interstitial fibrosis, accumulation of cell cycle-arrested cells, and increased levels of oxidative stress. TGF-I31 signaling is involved in these processes. In this study, we investigated whether klotho overexpression improves these features in the kidneys of aging mice and examined the inhibitory effect of klotho on signaling molecules related to transforming growth of TGF-I31. Klotho transgenic (KLTG) and wild-type (WT) mice were used, and 8-wk-old and 24-mo-old mice were defined as young and aging, respectively. We found that klotho expression was decreased in aging WT mice, but it was maintained in aging KLTG mice. Klotho overexpression improved the survival of 24-mo-old mice. Although the serum Ca2 thorn level was significantly lower in aging KLTG mice than in aging WT mice, the serum phosphate level did not differ between these mice. Klotho overexpression attenuated the increases in blood pressure, serum blood urea nitrogen level, and serum creatinine level in aging mice. Interstitial fibrosis, accumulation of cell cycle-arrested cells, and oxidative stress did not differ between young KLTG and WT mice, but they were significantly suppressed in aging KLTG mice compared with aging WT mice. Furthermore, the expression of TGF-I31-related signaling molecules was increased in aging WT mice, whereas it was inhibited in aging KLTG mice. These data suggest that klotho overexpression protects against kidney aging along with suppression of TGF-I31 signaling pathways. NEW & NOTEWORTHY Klotho is considered as an antiaging protein, and its overexpression may be a candidate therapy for protection against kidney damage with advanced aging. Although multiple factors are involved in the aging process, we showed that klotho overexpression inhibited interstitial fibrosis, accumulation of cell cycle-arrested cells, and increased levels of oxidative stress in the kidneys of aging mice, suppressing transforming growth factor-I31-related signaling pathways. The present data showed that klotho overexpression protects against age-associated kidney damage.

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