Investigation of trans-interaction between claudins, tight junction constitutive transmembrane proteins, and paracellular permeability.
| Project/Area Number |
23590249
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Multi-year Fund |
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| Section | 一般 |
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| Research Field |
General anatomy (including Histology/Embryology)
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| Research Institution | Fukuoka Dental College |
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Principal Investigator |
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| Co-Investigator(Kenkyū-buntansha) |
廣瀬 英司 明治国際医療大学, 公私立大学の部局等, 准教授 (40380620)
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| Project Period (FY) |
2011 – 2013
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2012: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2011: ¥2,470,000 (Direct Cost: ¥1,900,000、Indirect Cost: ¥570,000)
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| Keywords | tight junction / claudin / trans-interaction / permeability / タイト結合 / クローディン / 細胞間透過性 |
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| Research Abstract |
We established HEK293 cells, which does not form tight junctions (TJs), expressing RFP-cldn-1, RFP-cldn-10b, EGFP-cldn-10a or EGFP-cldn-10b. EGFP-cldn-10a- and RFP-cldn-1-expressing cells, EGFP-cldn-10b- and RFP-cldn-1-expressing cells, or EGFP-cldn-10a- and RFP-cldn-10b-expressing cells were co-cultured and examined by confocal laser scanning microscopy. Both EGFP-cldn-10a and EGFP-cldn-10b were not co-localized with RFP-cldn-1 in cell-cell contacts between heterotypic cells. In contrast, EGFP-cldn-10a was co-localized with RFP-cldn-10b. Using freeze-fracture electron microscopy, P-face-associated or E- face-associated TJ particles were observed in EGFP-cldn-10a- or EGFP-cldn-10b-expressing cells, respectively. When cldn-10a or cldn-10b was expressed in TJ-bearing MDCK I cells, cldn-10a did not alter trans-epithelial electrical resistance (TER), but cldn-10b markedly reduced TER.
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Report
(4 results)
Research Products
(13 results)
