Hypertensive Nephropathy (HN) is the second leading cause of chronic kidney disease (CKD) resistant to effective intervention to prevent progression. However, recent advances in regenerative medicine with the use of adipose tissue-derived mesenchymal stromal/stem cell (AD-MSC) transplantation offer hope for these patients. The MSCs have anti-fibrotic, anti-inflammatory, and pro-angiogenic paracrine activities that improve regeneration in some kidney injury models. However, exposure to patient-specific factors, such as aging and the uremic milieu of CKD in HN, may exert epigenetic and transcriptional modulation of MSC, potentially modifying their phenotype to one noxious to neighboring cells. Hence, increased cellular damage in HN may substantially compromise MSC function and become a barrier to successful autologous MSC transplantation. Our central hypothesis underlying this proposal is that MSCs obtained from patients with HN show impaired functionality and angiogenesis, which can be modified with hypoxic preconditioning (HPC). This hypothesis will be addressed both in vitro and in vivo in three specific aims: 1) we will compare functionality of MSCs from patients with HN (eGFR 15-60 mL/min/1.73m2) to MSC from age- and sex-matched patients with hypertension and healthy controls; 2) to determine the reversibility of HN-MSC dysfunction, we will subject cells from these cohorts to HPC in vitro and assess MSC function thereafter; and 3) to examine the effect of MSC function in vivo, we will conduct an experimental study in a porcine renovascular hypertension model that recapitulates the pathophysiology of HN, six-weeks after induction of renal artery stenosis. These pigs, as well as normal age-matched pigs, will be treated with HPC-MSC, untreated-MSC, or vehicle. To assess the impact of HPC on MSC potency, renal hemodynamics, function, and oxygenation will be studied after four-weeks, using sophisticated in vivo CT and MR imaging techniques, and renal injury and vascularity studied ex vivo. The significance of the proposed studies is high, since developing a safe and effective therapy to delay HN progression could reduce morbidity associated with dialysis, offer a better treatment option to a population often deferred for kidney transplantation, and produce extensive cost savings. These novel studies will advance the knowledge of the effects of HPC on MSC and their deleterious microenvironment, aid in developing a completely novel therapeutic strategy to delay the progression of HN supporting the NIDDK mission. The proposed project addresses how characterize and improve the functional properties of MSC in HN to allow these patients to benefit from future enrollment in clinical trials using stem cell transplantation. The exceptional resources and institutional support at Mayo Clinic, outstanding multi-disciplinary mentorship team, and proposed career development activities will allow the candidate to achieve her long-term goal of becoming an independent investigator and a nationally recognized leader in regenerative medicine in nephrology.

Public Health Relevance

Developing safe and effective therapies to delay and/or reduce the progression of chronic kidney disease (CKD) has tremendous potential to reduce the morbidity and mortality associated with end-stage renal disease (ESRD). In this application, we will explore the effect of hypertension, a leading risk factor for CKD, accompanied by kidney dysfunction, on human adult stem cells, as well as a novel method aimed towards the improvement of their function. Characterizing and optimizing the functional properties of stem cells in this population will allow for future clinical trials using stem-cell transplantation as a new and effective therapeutic strategy against CKD and ESRD.

National Institute of Health (NIH)
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Clinical Investigator Award (CIA) (K08)
Project #
Application #
Study Section
Special Emphasis Panel (ZDK1)
Program Officer
Rankin, Tracy L
Project Start
Project End
Budget Start
Budget End
Support Year
Fiscal Year
Total Cost
Indirect Cost
Mayo Clinic, Rochester
United States
Zip Code