The biomarker candidates of latent tuberculosis in exosomes from human serum
Project/Area Number |
15K15132
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Bacteriology (including mycology)
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Research Institution | Kyoto Prefectural University |
Principal Investigator |
Osada-Oka Mayuko 京都府立大学, 生命環境科学研究科, 准教授 (40347498)
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Project Period (FY) |
2015-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥3,770,000 (Direct Cost: ¥2,900,000、Indirect Cost: ¥870,000)
Fiscal Year 2016: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2015: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
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Keywords | 結核 / マクロファージ / エキソソーム / バイオマーカー / 潜在性結核 / exosome |
Outline of Final Research Achievements |
The asymptomatic group, which is called latent infection of Mycobacterium tuberculosis (LITB), is recognized as vitally important in controlling TB, because a majority of cases develop from latent infections. Thus, it has been required new diagnostic method to exactly establish LTBI. In this study, we examined the biomarker-targeted protein into macrophage-derived exosomes. After infection with active or latent Mycobacterium bovis Bacillus Calmette-Guerin, the expressions of both inflammatory and uninflammatory factor were up-regulated in RAW264.7 macrophages. Therefore, the protein were increased in exosomes from BCG-infected macrophages (BCG-exo) compared with exosomes from uninfected macrophages (none-exo). Moreover, it was identified 9 proteins, which is in BCG-exo derived from BCG-infected macrophages.
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Report
(3 results)
Research Products
(16 results)
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[Journal Article] A New Screen for Tuberculosis Drug Candidates Utilizing a Luciferase-Expressing Recombinant Mycobacterium bovis Bacillus Calmette-Guéren.2015
Author(s)
2)Ozeki Y, Igarashi M, Doe M, Tamaru A, Kinoshita N, Ogura Y, Iwamoto T, Sawa R, Umekita M, Enany S, Nishiuchi Y, Osada-Oka M, Hayashi T, Niki M, Tateishi Y, Hatano M, Matsumoto S.
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Journal Title
PLoS One
Volume: 10
Pages: 214-221
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Myeloid HIF-1 attenuates the progression of renal fibrosis in murine obstructive nephropathy.2015
Author(s)
Tateishi,Y, Osada-Oka M, Tanaka M, Shiota M, Izumi Y, Ishimura E, Motoyama K, Inaba M, Miura, K.
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Journal Title
J Pharmacol Sci
Volume: 127
Issue: 2
Pages: 181-189
DOI
Related Report
Peer Reviewed / Open Access
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