講演・口頭発表等[R]

基本情報

氏名 懸川 友人
氏名(カナ) カケガワ トモヒト
氏名(英語) Kakegawa Tomohito
所属 薬学部 医療薬学科
職名 教授
researchmap研究者コード
researchmap機関

タイトル

Effects of Clarithromycin on translatome of LPS-treated or untreated B-lymphoblastoid cells 

講演者

 

会議名

第87回日本薬理学会年会(仙台)

発表年月日

2014/03/18

開催年月日(From)

 

開催年月日(To)

 

招待の有無

 

記述言語

 

国名

 

会議区分

 

国際共著

 

会議種別

 

主催者

 

開催地

 

URL

形式

URL

無償ダウンロード

 

概要

Macrolides are known for immunomodulatory and anti-inflammatory actions. To analyze Clarithromycin (CAM) mechanism of action, we examined the effects of CAM on translatome of LPS-treated or untreated B-lymphoblastoid cells (BJAB). Translatome analyses were performed in 4 groups, i.e., LPS-treated or untreated (saline) BJAB, and cells further added with saline or CAM:LPS-saline(S), LPS-CAM, S-CAM, S-S. The cytoplasmic extracts were fractionated by sucrose gradient-centrifugation and divided into ten fractions, for RNA extraction. The RNAs extracted from polysome fractions were subjected to DNA microarray analysis.
GenMAPP Pathway-analysis (Filgen) showed significant gene expression changes in LPS-S, LPS-CAM and S-CAM. Analysis of mRNA-processing pathway showed that many gene expressions were modulated by CAM: 44 kinds of genes (factors associated with transcription factors, mRNA transcription and splicing factors, SR-proteins, and maturation and stability factors). Significant expression changes were seen in inflammation-related genes, such as IL-3, IL-5, EGF-EGFR, and EPO receptor pathway, in LPS-CAM. As mentioned above, it is likely that CAM controls inflammation pathway specifically in LPS-pretreated cells.

(共同研究につき本人担当部分の抽出不可能)

主要業績フラグ