| Project/Area Number |
25893155
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| Research Category |
Grant-in-Aid for Research Activity Start-up
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| Allocation Type | Single-year Grants |
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| Research Field |
Laboratory medicine
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| Research Institution | The University of Tokushima |
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Principal Investigator |
SAKURAI Akiko 徳島大学, ヘルスバイオサイエンス研究部, 助教 (70707900)
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| Project Period (FY) |
2013-08-30 – 2015-03-31
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| Project Status |
Completed (Fiscal Year 2014)
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| Budget Amount *help |
¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Fiscal Year 2014: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
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| Keywords | 糖尿病性腎症 / ポドサイト / バイオマーカー / CXCR4 / BMP4 |
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| Outline of Final Research Achievements |
Chronic kidney disease (CKD) is an important condition in the whole world not only in our country. It is very urgent to develop effective therapies based on the molecular mechanisms undeylying the onset and progression of CKD, especially regarding diabetic nephropathy (DMN). For this purpose, it is essential to identify the target molecule which plays central role for the pathophisiology. Focusing on the podocytes which induce direct causes of the significant renal function decline and proteinuria, we investigated the molecular basis of the novel target molecules (CXCR4 and CXCR7) in diabetic nephropathy.CXCR7 was expressed in podocytes of kidney glomeruli and was excreted in the urine in diabetic nephropathy. Moreover, the expression levels of CXCR7 was decreased in glomeruli during the course of the progression of nephropathy.
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