This application is submitted in response to RFA-HL-10-027. As indicated in the RFA announcement, """"""""The goals of this RFA are to elucidate, in animal models, the cellular and molecular mechanisms that underlie large artery stiffening and determine the role of arterial stiffening in the etiology of hypertension"""""""". Klotho is a recently-discovered anti-aging gene. Genetic mutation of klotho results in multiple premature aging phenotypes while overexpression of klotho extends lifespan. Cardiovascular disease is associated with aging. In humans, the prevalence of arterial stiffening and hypertension increases with age while the level of circulating klotho decreases with age. It is not known, however, if klotho is involved in the maintenance of normal arterial compliance. Whether klotho gene deficiency causes arterial stiffening has never been determined. Chronic kidney disorders are associated with arterial stiffening. Our new preliminary studies showed that conditional kidney- specific knockout of klotho gene (KL-KO) caused arterial stiffening and systolic hypertension. The objective of the proposed research is to determine the role of kidney-derived klotho in the maintenance of arterial compliance and the molecular mechanisms that mediate klotho deficiency-induced arterial stiffening and its relationship to the development of hypertension. This objective will be achieved by pursuing three coherent specific aims using a combination of experimental approaches including conditional kidney-specific gene knockout, in vivo gene delivery, and real-time monitoring of blood pressure (telemetry). (1) Determine the contribution of impaired endothelial function (down-regulation of eNOS) and oxidative stress (up-regulation of NADPH oxidase p47phox) to the KL-KO-induced arterial stiffening and systolic hypertension. (2) Determine the role of the up-regulation of MMP-9, TGF-21, and runt-related transcription factor-2 (RUNX-2) in SMCs and their relationship in KL-KO- induced elastin degradation, osteoblastic transition, calcification (elastocalcinosis), and arterial stiffening and systolic hypertension. (3) Determine the effects of therapeutic prevention of a decline in the circulating klotho on the development of arterial stiffening and systolic hypertension in senescence-accelerated mice P1 (SAMP1). The proposed studies are significant as they will reveal, for the first time, an important role of klotho deficiency in the pathogenesis of arterial stiffening. These studies will also demonstrate that arterial stiffening could be an important etiological factor in the development of systolic hypertension. Completion of the project may provide new insights into the therapeutic strategies for the control of arterial stiffening and related cardiovascular complications.

Public Health Relevance

Arterial stiffening and related cardiovascular disease is associated with aging and diabetes and is the major cause of death in the US. Indeed, the prevalence of arterial stiffening and hypertension increases with age. The purpose of the proposed research is to determine the role of klotho, a recently-discovered anti-aging gene, in the pathogenesis of large, conduit artery stiffening and its relationship to development of systolic hypertension. The results will provide novel information regarding the molecular mechanism of large artery stiffening in klotho-deficient animals. Completion of the project may offer a new therapeutic approach for large artery stiffening and related cardiovascular disorders. The finding will benefit the US population which has a high prevalence of cardiovascular disease.

National Institute of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)
Research Project (R01)
Project #
Application #
Study Section
Special Emphasis Panel (ZHL1-CSR-W (S1))
Program Officer
OH, Youngsuk
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
University of Oklahoma Health Sciences Center
Schools of Medicine
Oklahoma City
United States
Zip Code
Chen, Jianglei; Fan, Jun; Wang, Shirley et al. (2018) Secreted Klotho Attenuates Inflammation-Associated Aortic Valve Fibrosis in Senescence-Accelerated Mice P1. Hypertension 71:877-885
Jung, Dongju; Xu, Yuechi; Sun, Zhongjie (2017) Induction of anti-aging gene klotho with a small chemical compound that demethylates CpG islands. Oncotarget 8:46745-46755
Oh, Young S; Berkowitz, Dan E; Cohen, Richard A et al. (2017) A Special Report on the NHLBI Initiative to Study Cellular and Molecular Mechanisms of Arterial Stiffness and Its Association With Hypertension. Circ Res 121:1216-1218
Lin, Yi; Chen, Jianglei; Sun, Zhongjie (2016) Antiaging Gene Klotho Deficiency Promoted High-Fat Diet-Induced Arterial Stiffening via Inactivation of AMP-Activated Protein Kinase. Hypertension 67:564-73
Varshney, Rohan; Ali, Quaisar; Wu, Chengxiang et al. (2016) Monocrotaline-Induced Pulmonary Hypertension Involves Downregulation of Antiaging Protein Klotho and eNOS Activity. Hypertension 68:1255-1263
Chen, Jianglei; Lin, Yi; Sun, Zhongjie (2016) Deficiency in the anti-aging gene Klotho promotes aortic valve fibrosis through AMPK?-mediated activation of RUNX2. Aging Cell 15:853-60
Gao, Diansa; Zuo, Zhong; Tian, Jing et al. (2016) Activation of SIRT1 Attenuates Klotho Deficiency-Induced Arterial Stiffness and Hypertension by Enhancing AMP-Activated Protein Kinase Activity. Hypertension 68:1191-1199
Zhou, Xiaoli; Chen, Kai; Wang, Yongjun et al. (2016) Antiaging Gene Klotho Regulates Adrenal CYP11B2 Expression and Aldosterone Synthesis. J Am Soc Nephrol 27:1765-76
Fan, Jun; Sun, Zhongjie (2016) The Antiaging Gene Klotho Regulates Proliferation and Differentiation of Adipose-Derived Stem Cells. Stem Cells 34:1615-25
Lin, Yi; Sun, Zhongjie (2015) Antiaging Gene Klotho Attenuates Pancreatic ?-Cell Apoptosis in Type 1 Diabetes. Diabetes 64:4298-311

Showing the most recent 10 out of 28 publications