Abstract | BACKGROUND: METHODS: Glomeruli were microdissected from renal biopsies from 24 patients with DN and 8 donor controls. The expression of ANGPTL2 was assessed by RT-PCR and immunohistochemistry, and then correlated with clinical and pathological indices of glomerular injury. RESULTS: Consistent with the results of the gene chip experiment, abundant expression of ANGPTL2 was found more frequently in diabetic glomeruli as compared to donor controls (95 vs. 38%, chi(2) = 15.9, p < 0.01). ANGPTL2 mRNA upregulation was more prominent in glomeruli with less microaneurysm (22 vs. 66%, p < 0.05), inflammatory influx (6 vs. 50%, p < 0.05) or endothelial foam cell formation (11 vs. 53%, p < 0.05). Immunostaining revealed an upregulation of ANGPTL2 protein in hypertrophied diabetic glomeruli, mainly distributed in podocytes, which were supposed to be the origin of ANGPTL2. CONCLUSION: The upregulation of ANGPTL2 in diabetic glomerulopathy shows a close relationship to abnormal microvasculature and endothelial inflammation. ANGPTL2 may play an important role in the pathogenesis of diabetic glomerulopathy.
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Authors | Hua Sun, Jing-min Zheng, Shan Chen, Cai-hong Zeng, Zhi-hong Liu, Lei-shi Li |
Journal | Nephron. Experimental nephrology
(Nephron Exp Nephrol)
Vol. 105
Issue 4
Pg. e117-23
( 2007)
ISSN: 1660-2129 [Electronic] Switzerland |
PMID | 17347581
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright 2007 S. Karger AG, Basel. |
Chemical References |
- ANGPTL2 protein, human
- Angiopoietin-Like Protein 2
- Angiopoietin-like Proteins
- Angiopoietins
- Intercellular Signaling Peptides and Proteins
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Topics |
- Angiopoietin-Like Protein 2
- Angiopoietin-like Proteins
- Angiopoietins
- Diabetic Nephropathies
(genetics, metabolism)
- Female
- Gene Expression Profiling
- Genetic Predisposition to Disease
(genetics)
- Humans
- In Vitro Techniques
- Intercellular Signaling Peptides and Proteins
(genetics, metabolism)
- Kidney Glomerulus
(blood supply, metabolism)
- Male
- Microcirculation
(metabolism)
- Middle Aged
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