2014 Fiscal Year Final Research Report
Significance of Podocyte Autophagy and Elucidation of Its Mechanism in Human Glomerular Diseases
Project/Area Number |
24591200
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Kidney internal medicine
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Research Institution | Okayama University |
Principal Investigator |
SUGIYAMA Hitoshi 岡山大学, 医歯(薬)学総合研究科, 教授 (60325090)
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Keywords | オートファジー / 糸球体上皮細胞 / ネフローゼ症候群 |
Outline of Final Research Achievements |
Autophagy is a cellular process involved in the bulk degradation of proteins and organelle turnover. This study aimed to elucidate the morphological evidence for autophagy and its association with ultrastructural alterations of podocytes and clinical parameters in patients with minimal change nephrotic syndrome (MCNS). Autophagic vacuoles were particularly detected in podocytes. Overall, the number of autophagic vacuoles in podocytes was significantly correlated with age. In the patients with MCNS, the number of autophagic vacuoles in podocytes was significantly correlated with the podocyte foot process effacement (FPE) score, the amount of proteinuria and the level of serum albumin. The number of autophagic vacuoles in podocytes was significantly increased in the patients with MCNS and MN in comparison to that observed in the patients with IgAN and LN. The data indicate that the autophagy of podocytes is associated with FPE and massive proteinuria in patients with MCNS.
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Free Research Field |
腎臓内科学
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