Hepatic and proximal tubule angiotensinogen play distinct roles in kidney dysfunction, glomerular and tubular injury, and fibrosis progression

Author:

Jang Hee-Seong123ORCID,Noh Mi Ra12ORCID,Plumb Troy4,Lee Kyung5ORCID,He John Cijiang5,Ferrer Fernando A.6,Padanilam Babu J.12ORCID

Affiliation:

1. Department of Urology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York

2. Department of Cellular and Integrative Physiology, University of Nebraska Medical Center, Omaha, Nebraska

3. Division of Pediatric Surgery, Department of Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland

4. Division of Nephrology, Internal Medicine, University of Nebraska Medical Center, Omaha, Nebraska

5. Division of Nephrology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York

6. Department of Urology, Kravis Children’s Hospital, Icahn School of Medicine at Mount Sinai, New York, New York

Abstract

Chronic kidney disease (CKD) is a major unmet medical need with no effective treatment. Current findings demonstrate that hepatic and proximal tubule angiotensinogen have distinct roles in tubular and glomerular injury, fibrogenesis, and renal dysfunction during CKD development. As renin-angiotensin system components, including angiotensinogen, are important targets for treating CKD in the clinic, the results from our study may be applied to developing better tissue-targeted treatment strategies for CKD and other fibroproliferative diseases.

Funder

American Heart Association

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

American Physiological Society

Subject

Physiology

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