Protective Role of Endogenous Kallistatin in Vascular Injury and Senescence by Inhibiting Oxidative Stress and Inflammation

Kallistatin was identified in human plasma as a tissue kallikrein‐binding protein and a serine proteinase inhibitor. Kallistatin exerts pleiotropic effects on angiogenesis, oxidative stress, inflammation, apoptosis, fibrosis, and tumor growth. Kallistatin levels are markedly reduced in patients with coronary artery disease, sepsis, diabetic retinopathy, inflammatory bowel disease, pneumonia, and cancer. Moreover, plasma kallistatin levels are positively associated with leukocyte telomere length in young African Americans, indicating the involvement of kallistatin in aging. In addition, kallistatin treatment promotes vascular repair by increasing the migration and function of endothelial progenitor cells (EPCs). Kallistatin via its heparin‐binding site antagonizes TNF‐α‐induced senescence and superoxide formation, while kallistatin’s active site is essential for inhibiting miR‐34a synthesis, thus elevating sirtuin 1 (SIRT1)/eNOS synthesis in EPCs. Kallistatin inhibits oxidative stress‐induced cellular senescence by upregulating Let‐7g synthesis, leading to modulate Let‐7g‐mediated miR‐34a‐SIRT1‐eNOS signaling pathway in human endothelial cells. Exogenous kallistatin administration attenuates vascular injury and senescence in association with increased SIRT1 and eNOS levels and reduced miR‐34a synthesis and NADPH oxidase activity, as well as TNF‐α and ICAM‐1 expression in the aortas of streptozotocin‐ (STZ‐) induced diabetic mice. Conversely, endothelial‐specific depletion of kallistatin aggravates vascular senescence, oxidative stress, and inflammation, with further reduction of Let‐7g, SIRT1, and eNOS and elevation of miR‐34a in mouse lung endothelial cells. Furthermore, systemic depletion of kallistatin exacerbates aortic injury, senescence, NADPH oxidase activity, and inflammatory gene expression in STZ‐induced diabetic mice. These findings indicate that endogenous kallistatin displays a novel role in protection against vascular injury and senescence by inhibiting oxidative stress and inflammation.