Establishment of ELISA that detect polymeric OPN and its usefulness
| Project/Area Number |
26670280
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| Research Category |
Grant-in-Aid for Challenging Exploratory Research
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| Allocation Type | Multi-year Fund |
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| Research Field |
Laboratory medicine
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| Research Institution | Hiroshima University |
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Principal Investigator |
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| Co-Investigator(Renkei-kenkyūsha) |
Nishimichi Norihisa 広島大学, 保健管理センター, 研究員 (00583486)
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| Project Period (FY) |
2014-04-01 – 2016-03-31
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| Project Status |
Completed (Fiscal Year 2015)
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| Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2015: ¥1,300,000 (Direct Cost: ¥1,000,000、Indirect Cost: ¥300,000)
Fiscal Year 2014: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
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| Keywords | オステオポンチン / 重合 / ELISA / 好中球 / ポリマー / トランスグルタミナーゼ / 重合体 / 抗体 |
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| Outline of Final Research Achievements |
To establish a new ELISA that detects polymeric osteopontin, which we previously found as a chemoattractant for neutrophils, we attempted to obtain polymeric OPN specific monoclonal antibodies. First we generated mice that express only polymerization-incompetent OPN by introducing some mutations into the OPN gene. The mice produced many antibody clones responding to injected polymeric OPN. However, many of clones recognized wild type OPN, which prevent us from establish the specific clones. Probably, immunological tolerance was not sufficient for the mice not to respond wild type OPN. We restarted to generate the tolerant mice by CRISPR-Cas9 method.
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Report
(3 results)
Research Products
(21 results)
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[Journal Article] Periostin promotes hepatic fibrosis in mice by modulating hepatic stellate cell activation via αv integrin interaction.2016
Author(s)
Soltani AK, McCarthy DA, McKleroy W, Azary S, Sakuma S, Ha A, Tharp K, Yokosaki Y, Hart D, Stahl A, Atabai K.
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Journal Title
DOI
Related Report
Peer Reviewed / Open Access / Int'l Joint Research
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