Accumulation of Advanced Oxidation Protein Products Promotes Age-Related Decline of Type H Vessels in Bone.

Kai Zhao, Guo-Zheng Zhu, Hong-Zhou Li, Jia-Wen Gao, Chen Tu, Di-Zheng Wu, Yu-Sheng Huang, Dong Han, Xing-Yu Chen, Long-Yan Wu, Zhao-Ming Zhong
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Abstract

Type H vessels have been proven to couple angiogenesis and osteogenesis. The decline of type H vessels contributes to bone loss in the aging process. Aging is accompanied by the accumulation of advanced oxidation protein products (AOPPs). However, whether AOPP accumulation is involved in age-related decline of type H vessels is unclear. Here, we show that the increase of AOPP levels in plasma and bone was correlated with the decline of type H vessels and loss of bone mass in old mice. Exposure of microvascular endothelial cells to AOPPs significantly inhibited cell proliferation, migration, and tube formation; increased NADPH oxidase activity and excessive reactive oxygen species generation; upregulated the expression of vascular cell adhesion molecule-1 and intercellular cell adhesion molecule-1; and eventually impaired angiogenesis, which was alleviated by redox modulator N-acetylcysteine and NADPH oxidase inhibitor apocynin. Furthermore, reduced AOPP accumulation by NAC treatment was able to alleviate significantly the decline of type H vessels, bone mass loss, and deterioration of bone microstructure in old mice. Collectively, these findings suggest that AOPPs accumulation contributes to the decline of type H vessels in the aging process, and illuminate a novel potential mechanism underlying age-related bone loss.

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高级氧化蛋白产物的积累会促进骨骼中 H 型血管与年龄相关的衰退。
H 型血管已被证明与血管生成和骨生成密切相关。在衰老过程中,H 型血管的衰退会导致骨质流失。衰老伴随着高级氧化蛋白产物(AOPPs)的积累。然而,AOPP 的积累是否参与了与年龄相关的 H 型血管衰退还不清楚。在这里,我们发现血浆和骨骼中 AOPP 水平的增加与老龄小鼠 H 型血管的衰退和骨量的损失有关。微血管内皮细胞暴露于 AOPPs 会显著抑制细胞增殖、迁移和管形成,增加 NADPH 氧化酶活性和过量活性氧的生成,上调血管细胞粘附分子-1 和细胞间粘附分子-1 的表达,并最终阻碍血管生成,而氧化还原调节剂 N-乙酰半胱氨酸和 NADPH 氧化酶抑制剂阿朴西宁可缓解这种情况。此外,通过 NAC 处理减少 AOPP 的积累能够显著缓解老龄小鼠 H 型血管的衰退、骨量减少和骨微结构的恶化。总之,这些研究结果表明,AOPPs 的积累是导致 H 型血管在衰老过程中衰退的原因之一,并揭示了与年龄相关的骨质流失的一种新的潜在机制。
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