Klotho Ameliorates Vascular Calcification via Promoting Autophagy.

Oxid Med Cell Longev

Institute of Cardiovascular Research, Xinqiao Hospital, Army Medical University, Chongqing 400037, China.

Published: February 2023

AI Article Synopsis

  • Vascular calcification (VC) is linked to aging and is worsened by a lack of Klotho, a protein that can be restored to alleviate VC symptoms.
  • Research shows that low Klotho levels correlate with increased aortic calcification, and Klotho-deficient mice experience VC that improves with Klotho protein supplementation.
  • Increased autophagy is observed in Klotho-deficient mice, protecting them from VC, and Klotho aids in reducing calcification by enhancing autophagy in both these mice and vascular smooth muscle cells.

Article Abstract

Vascular calcification (VC) is regarded as a common feature of vascular aging. Klotho deficiency reportedly contributes to VC, which can be ameliorated by restoration of Klotho expression. However, the specific mechanisms involved remain unclear. Here, we investigated the role of autophagy in the process of Klotho-inhibiting VC. The clinical study results indicated that, based on Agatston score, serum Klotho level was negatively associated with aortic calcification. Then, Klotho-deficient mice exhibited aortic VC, which could be alleviated with the supplementation of Klotho protein. Moreover, autophagy increased in the aorta of Klotho-deficient mice and protected against VC. Finally, we found that Klotho ameliorated calcification by promoting autophagy both in the aorta of Klotho-deficient mice and in mouse vascular smooth muscle cells (MOVAS) under calcifying conditions. These findings indicate that Klotho deficiency induces increased autophagy to protect against VC and that Klotho expression further enhances autophagy to ameliorate calcification. This study is beneficial to exploring the underlying mechanisms of Klotho regulating VC, which has important guiding significance for future clinical studies in the treatment of VC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9629936PMC
http://dx.doi.org/10.1155/2022/7192507DOI Listing

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