Localization of a cyclopentenone prostaglandin to the endoplasmic reticulum and induction of BiP mRNA

被引:29
作者
Takahashi, S
Odani, N
Tomokiyo, K
Furuta, K
Suzuki, M
Ichikawa, A
Negishi, M [1 ]
机构
[1] Kyoto Univ, Fac Pharmaceut Sci, Dept Mol Neurobiol, Sakyo Ku, Kyoto 6068501, Japan
[2] Gifu Univ, Fac Engn, Dept Biomol Sci, Gifu 5011112, Japan
[3] Kyoto Univ, Fac Pharmaceut Sci, Dept Physiol Sci, Sakyo Ku, Kyoto 6068501, Japan
关键词
D O I
10.1042/bj3350035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cyclopentenone prostaglandins (PGs) are transported into cells and stimulate the expression of various stress genes, such as that coding for BiP (an ER luminal protein). To reveal the site of action of the PGs for the induction of stress-gene expression, we introduced a fluorescent probe, pyrene, into two types of PG analogue, GIF0010 (a cyclopentenone type) and GIF0037 (a cyclopentanone type) and examined their intracellular localization in normal rat kidney cells and their ability to induce the BiP gene expression. GIF0010 accumulated around the nuclei and coincided with BiP, a resident protein in the endoplasmic reticulum (ER) and markedly induced BiP gene expression. By contrast, GIF0037 and pyrene neither accumulated in the cell nor induced BiP gene expression. Thus the ER localization of GIF0010 and the induction of gene expression by GIF0010 are ascribed to the cyclopentenone structure. Treatment with cycloheximide inhibited both the accumulation of GIF0010 and the induction of the BiP mRNA, suggesting that the ER localization of the PG and subsequent gene expression require the nascent protein synthesis. These results demonstrate that the cyclopentenone PG is specifically accumulated in the ER, transducing a signal for BiP gene expression in the nuclei.
引用
收藏
页码:35 / 42
页数:8
相关论文
共 39 条
[21]   Signalling from endoplasmic reticulum to nucleus: Transcription factor with a basic-leucine zipper motif is required for the unfolded protein-response pathway [J].
Mori, K ;
Kawahara, T ;
Yoshida, H ;
Yanagi, H ;
Yura, T .
GENES TO CELLS, 1996, 1 (09) :803-817
[22]  
NARUMIYA S, 1987, J PHARMACOL EXP THER, V242, P306
[23]  
NARUMIYA S, 1986, J PHARMACOL EXP THER, V239, P500
[24]  
NARUMIYA S, 1986, J PHARMACOL EXP THER, V239, P506
[25]  
NEEDLEMAN P, 1986, ANNU REV BIOCHEM, V55, P69, DOI 10.1146/annurev.biochem.55.1.69
[26]   MOLECULAR MECHANISMS OF DIVERSE ACTIONS OF PROSTANOID RECEPTORS [J].
NEGISHI, M ;
SUGIMOTO, Y ;
ICHIKAWA, A .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1995, 1259 (01) :109-119
[27]   BIOLOGICAL ACTIONS OF DELTA(12)-PROSTAGLANDIN J(2) [J].
NEGISHI, M ;
KOIZUMI, T ;
ICHIKAWA, A .
JOURNAL OF LIPID MEDIATORS AND CELL SIGNALLING, 1995, 12 (2-3) :443-448
[28]   Induction of protein disulfide isomerase mRNA by Delta(12)-prostaglandin J(2) [J].
Odani, N ;
Negishi, M ;
Takahashi, S ;
Ichikawa, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 220 (02) :264-268
[29]   Regulation of BiP gene expression by cyclopentenone prostaglandins through unfolded protein response element [J].
Odani, N ;
Negishi, M ;
Takahashi, S ;
Kitano, Y ;
Kozutsumi, Y ;
Ichikawa, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (28) :16609-16613
[30]   JIP60, A METHYL JASMONATE-INDUCED RIBOSOME-INACTIVATING PROTEIN INVOLVED IN PLANT STRESS REACTIONS [J].
REINBOTHE, S ;
REINBOTHE, C ;
LEHMANN, J ;
BECKER, W ;
APEL, K ;
PARTHIER, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (15) :7012-7016