Effect of Tissue-derived Angiotensinogen on Kidney Injury and Fibrosis in Obstructive Nephropathy

• Published in: In vivo (Athens) Vol. 38; no. 5; pp. 2107 - 2114
• Main Authors: Jang, Hee-Seong, Noh, Mi Ra, Ha, Ligyeom, Kim, Jinu, Padanilam, Babu J
• Format: Journal Article
• Language: English
• Published: Greece 01.09.2024
• Subjects: Angiotensinogen - genetics; Angiotensinogen - metabolism; Animals; Disease Models, Animal; Fibrosis; Kidney - metabolism; Kidney - pathology; Kidney Diseases - etiology; Kidney Diseases - genetics; Kidney Diseases - metabolism; Kidney Diseases - pathology; Kidney Tubules, Proximal - metabolism; Kidney Tubules, Proximal - pathology; Liver - metabolism; Liver - pathology; Low Density Lipoprotein Receptor-Related Protein-2 - genetics; Low Density Lipoprotein Receptor-Related Protein-2 - metabolism; Mice; Mice, Knockout; Ureteral Obstruction - complications; Ureteral Obstruction - genetics; Ureteral Obstruction - metabolism; Ureteral Obstruction - pathology; Obstructive nephropathy; ureteral obstruction; kidney injury; angiotensinogen; kidney fibrosis
• ISSN: 0258-851X; 1791-7549; 1791-7549
• DOI: 10.21873/invivo.13672

Angiotensinogen (AGT), a precursor of angiotensin II (AngII), contributes to regulating (patho)physiological conditions, including blood pressure changes, inflammation, and kidney fibrosis. However, the precise role of tissue-specific AGT in kidney fibrosis independent of blood pressure remains to be fully understood. This study investigated the source of intrarenal AGT and its role in kidney injury and fibrosis during obstructive nephropathy. Proximal tubule- (PT, major source secreting AGT in the kidney; PKO) or liver- (major source of circulating AGT; LKO) AGT knockout (KO) mice were subjected to unilateral ureteral obstruction (UUO), a blood pressure-independent fibrosis model. UUO increased AGT mRNA and protein levels in the kidneys. PKO decreased AGT mRNA, but LKO enhanced it in UUO kidneys compared with the control. In contrast, the intrarenal protein levels of AGT increased in PKO, but not in LKO in UUO kidneys, indicating that the liver is a major source of intrarenal AGT protein. Expression of megalin, a PT receptor involved in the uptake of circulating AGT, was down-regulated in UUO kidneys and was independent of PKO or LKO. However, none of these changes prevented UUO-induced tubular injury and kidney fibrosis. Hepatic and proximal tubule AGT play distinct roles in contributing to intrarenal AGT levels during UUO, and their genetic inhibitions fail to prevent kidney injury and fibrosis, suggesting a highly complicated signaling pathway of the renin-angiotensin system and an associated compensatory mechanism in obstructive nephropathy.