Kidney angiopoietin-like protein 4 regulates fibrotic responses in diabetic kidney disease

The angiopoietin-like (ANGPTL) proteins are now recognized as critical regulators of the harmful changes seen in diabetic kidney disease. Notably, a hyposialylated pro-proteinuric form of ANGPTL4 has been identified as a crucial contributor to fibrosis within diabetic kidneys. Under diabetic conditions, glomerular podocytes secrete this hyposialylated ANGPTL4, which plays a significant role in disrupting lipid metabolism, promoting inflammation, and driving fibrosis in both podocytes and adjacent tubules. This secreted ANGPTL4 interacts with tubular cells via Integrin-1 and DPP-4, causing mitochondrial damage that activates the c-GAS-STING pathway and exacerbates inflammation. Importantly, targeting renal ANGPTL4 with antisense oligonucleotides (ASOs) has shown promising protective effects against fibrosis in diabetic kidneys, paving the way for innovative therapeutic strategies to combat diabetic kidney disease and other fibrotic disorders.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2026-04-15
DOI
https://doi.org/10.3389/fphar.2026.1803412
Primary Topic
Lipid metabolism and disorders
Type
article
Field-Weighted Citation Impact
0.00
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Kidney angiopoietin-like protein 4 regulates fibrotic responses in diabetic kidney disease

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Kidney angiopoietin-like protein 4 regulates fibrotic responses in diabetic kidney disease

Ken Inoki, Swayam Prakash Srivastava, Shangyang Xia, Mariam Hamed, Shota Yoshida, Adesh Urval, Aashika Dupati, Ajan Vishnu Arora
article en

Abstract

The angiopoietin-like (ANGPTL) proteins are now recognized as critical regulators of the harmful changes seen in diabetic kidney disease. Notably, a hyposialylated pro-proteinuric form of ANGPTL4 has been identified as a crucial contributor to fibrosis within diabetic kidneys. Under diabetic conditions, glomerular podocytes secrete this hyposialylated ANGPTL4, which plays a significant role in disrupting lipid metabolism, promoting inflammation, and driving fibrosis in both podocytes and adjacent tubules. This secreted ANGPTL4 interacts with tubular cells via Integrin-1 and DPP-4, causing mitochondrial damage that activates the c-GAS-STING pathway and exacerbates inflammation. Importantly, targeting renal ANGPTL4 with antisense oligonucleotides (ASOs) has shown promising protective effects against fibrosis in diabetic kidneys, paving the way for innovative therapeutic strategies to combat diabetic kidney disease and other fibrotic disorders.

Frontiers in PharmacologyVol. 17
University of Michigan (US)
Good health and well-being
Openalex Percentile: Top 24%
Lipid metabolism and disorders
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