Project/Area Number |
11670583
|
Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Respiratory organ internal medicine
|
Research Institution | Nagasaki University |
Principal Investigator |
OISHI Kazunori Nagasaki University, Insitute of Tropical Medicine, Associate Professor, 熱帯医学研究所, 助教授 (80160414)
|
Co-Investigator(Kenkyū-buntansha) |
YOSHIMINE Hiroyuki Nagasaki University, School of Medicine, University Hospital, Assistant Professor, 医学部・附属病院, 助手 (30304950)
AMANO Hideaki Nagasaki University, Insitute of Tropical Medicine, Assistant Professor, 熱帯医学研究所, 助手 (00304949)
|
Project Period (FY) |
1999 – 2000
|
Project Status |
Completed (Fiscal Year 2000)
|
Budget Amount *help |
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 2000: ¥1,300,000 (Direct Cost: ¥1,300,000)
Fiscal Year 1999: ¥2,100,000 (Direct Cost: ¥2,100,000)
|
Keywords | Pseudomonas aeruginosa / IL-8 inducing proteins / Pulmonary epithelial cells / Chronic lower respiratory tract infections / 転写調節因子 |
Research Abstract |
In this study, we evaluated the IL-8 inducing capacity of the culture supernatants of a mucoid P.aeruginosa strain (CSPA), and purified the IL-8 inducing factors from CSPA in pulmonary epithelial cell-like cell line (A549 cells) which did not induce IL-8 production in response to stimualtion with LPS.We found a majority of IL-8 inducing capacity in the 10 th fraction ( MW ; 32〜56 kDa) of gel-filtration chromatography of the condensed CSPA with molecular mass (>30 kDa) after ammonium sulfate sedimentation (SAS). The biochemical analysis of this fraction revealed a slightly thermolabile protein. A similar biochemical character was found in a single IL-8 inducing fraction of serial ion-exchange chromoatography of SAS-CSPA.The silver stained SDS-PAGE gel revealed a single band with estimated molecular mass of 42 kDa. These data support that the major IL-8 inducing factor in the CSPA by A549 cell is a slightly thermolabile protein with estimated molecular mass of 42 kDa. Further studies require for the identification of this secretory protein and it's role in the pathogenesis of chronic lower respiratiry tract infections.
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