Project/Area Number |
10671341
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Orthopaedic surgery
|
Research Institution | Gunma University |
Principal Investigator |
SHINOZAKI Tetsuya Gunma University, Faculty of Medicine, Assistant Professor, 医学部, 講師 (90251115)
|
Co-Investigator(Kenkyū-buntansha) |
WATANABE Hideomi Gunma University, Faculty of Medicine, Assistant Professor, 医学部, 講師 (40231724)
TAKAGISHI Kenji Gunma University, Faculty of Medicine, Professor, 医学部, 教授 (70154763)
|
Project Period (FY) |
1998 – 2001
|
Project Status |
Completed (Fiscal Year 2001)
|
Budget Amount *help |
¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 2001: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 2000: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1999: ¥500,000 (Direct Cost: ¥500,000)
|
Keywords | Alkaline Phosphatase / serum / function / sugar chain / アルカリフォスファターゼ |
Research Abstract |
Alkaline phosphatase (ALP) is a glycoprotein enzyme which exists in most tissues and cells of the body. The biological functions of ALP and the significance of its sugar chains still remain unclear. At least four types of ALP have been identified, i.e. liver/bone/ kidney-type, intestinal-type, placental-type, and placental-like-type ALP. Each of type ALP has tissue specific functions. We postulated that their different functions are based on its different types of their sugar chains. Further, elevated serum ALP from the patients with osteosarcoma, which is the representative malignant bone tumor in the orthopedic area, would have some specific type of the sugar chain. The identification of its specific sugar chain might leads to the discovery of the specific marker to the osteosarocoma. We performed the isolation of serum ALP from the patients with various types of bone diseases with affinity chromatography using Blue Sepharose and Protein A. Isolated ALP was applied to SDS-PAGE followed by the Western Blotting with-a specific antibody to ALP. However, we couldn't identify the disease specific band. Further, we applied the HPLC with various types of lectins to discriminate the disease specific ALP based on its different sugar chain. However, little differentiation could not be obtained. Further experiments with different types of antibody, lectins, and elution conditions are necessary.
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