Murdoch University Research Repository

Welcome to the Murdoch University Research Repository

The Murdoch University Research Repository is an open access digital collection of research
created by Murdoch University staff, researchers and postgraduate students.

Learn more

CD70 exacerbates blood pressure elevation and renal damage in response to repeated hypertensive stimuli

Itani, H.A., Xiao, L., Saleh, M.A., Wu, J., Pilkinton, M.A., Dale, B.L., Barbaro, N.R., Foss, J.D., Kirabo, A., Montaniel, K.R., Norlander, A.E., Chen, W., Sato, R., Navar, L.G., Mallal, S.A., Madhur, M.S., Bernstein, K.E. and Harrison, D.G. (2016) CD70 exacerbates blood pressure elevation and renal damage in response to repeated hypertensive stimuli. Circulation Research, 118 . pp. 1233-1243.

PDF - Authors' Version
Download (1MB) | Preview
Free to read:
*No subscription required


Accumulating evidence supports a role of adaptive immunity and particularly T cells in the pathogenesis of hypertension. Formation of memory T cells, which requires the costimulatory molecule CD70 on antigen-presenting cells, is a cardinal feature of adaptive immunity.

To test the hypothesis that CD70 and immunologic memory contribute to the blood pressure elevation and renal dysfunction mediated by repeated hypertensive challenges.

We imposed repeated hypertensive challenges using either N(ω)-nitro-L-arginine methyl ester hydrochloride (L-NAME)/high salt or repeated angiotensin II stimulation in mice. During these challenges effector memory T cells (T(EM)) accumulated in the kidney and bone marrow. In the L-NAME/high-salt model, memory T cells of the kidney were predominant sources of interferon-γ and interleukin-17A, known to contribute to hypertension. L-NAME/high salt increased macrophage and dendritic cell surface expression of CD70 by 3- to 5-fold. Mice lacking CD70 did not accumulate T(EM) cells and did not develop hypertension to either high salt or the second angiotensin II challenge and were protected against renal damage. Bone marrow-residing T(EM) cells proliferated and redistributed to the kidney in response to repeated salt feeding. Adoptively transferred T(EM) cells from hypertensive mice homed to the bone marrow and spleen and expanded on salt feeding of the recipient mice.

Our findings illustrate a previously undefined role of CD70 and long-lived T(EM) cells in the development of blood pressure elevation and end-organ damage that occur on delayed exposure to mild hypertensive stimuli. Interventions to prevent repeated hypertensive surges could attenuate formation of hypertension-specific T(EM) cells

Item Type: Journal Article
Publisher: American Heart Association
Copyright: © 2016 American Heart Association, Inc.
Item Control Page Item Control Page


Downloads per month over past year