4.4 Article

Elevated Endostatin Expression Is Regulated by the pIgA Immune Complex and Associated with Disease Severity of IgA Nephropathy

Journal

KIDNEY & BLOOD PRESSURE RESEARCH
Volume 46, Issue 1, Pages 31-40

Publisher

KARGER
DOI: 10.1159/000508079

Keywords

IgA nephropathy; pIgA immune complex; Endostatin

Funding

  1. National Natural Science Foundation for Youths of China [81600555]
  2. China Postdoctoral Science Foundation [2018M640684]
  3. National Natural Science Foundation of China [81873611]
  4. Science and Technology Innovation Team of Henan [17IRTSTHN020]
  5. Foundation for Leading Personnel of Central Plains of China [194200510006]

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The study found that elevated levels of endostatin in patients with IgA nephropathy (IgAN) are associated with disease severity and poor prognosis. Endostatin may play an important role in the pathogenesis of IgAN.
Background/Aims: Renal vascular injury accounts for the poor outcomes of patients with IgA nephropathy (IgAN). In this study, we investigated whether endostatin, a potent inhibitor of angiogenesis, is associated with IgAN. Methods: Serum endostatin levels were detected in patients with IgAN, disease controls, and healthy controls, and the correlation among endostatin and clinicopathologic manifestations, as well as prognosis in patients with IgAN, was analyzed. In addition, serum endostatin levels were compared in patients before and after treatment. Data on endostatin expression in the renal interstitium of patients with IgAN were downloaded and analyzed from the GSE35489 array in the GEO database. The poly-IgA1 (pIgA) immune complex is widely recognized as the trigger of IgAN initiation. pIgA in the plasma of patients was extracted and used to stimulate human glomerular endothelial cells (GECs). Endostatin, IL-6, and CXCL1 in the cell supernatant were detected by ELISA kits. Results: We found that serum endostatin levels were significantly increased in patients with IgAN, as was endostatin expression in the renal interstitium. Patients with IgAN were divided into 2 groups according to the median value. The high endostatin expression group had significantly higher levels of serum creatinine and BUN and more severe tubular/interstitial damage. Moreover, patients with arteriolar injury and endothelial cell proliferation had higher serum endostatin levels. Patients with high serum endostatin levels had poor prognosis. According to the in vitro experiment, the GEC apoptosis rate and the supernatant levels of endostatin, IL-6, and CXCL1 were significantly increased following pIgA stimulation. Conclusion: Our study found that elevated endostatin expression was associated with disease severity and poor prognosis in patients with IgAN and can be upregulated by pIgA, but how it participates in the pathogenesis of IgAN deserves further exploration.

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