Transcriptional profiling of gene expression patterns during sphingosine 1-phosphate-induced mesangial cell proliferation

被引:21
|
作者
Katsuma, S
Hada, Y
Shiojima, S
Hirasawa, A
Tanoue, A
Takagaki, K
Ohgi, T
Yano, J
Tsujimoto, G
机构
[1] Natl Ctr Child Hlth, Dept Mol Cell Pharmacol, Setagaya Ku, Tokyo 1548567, Japan
[2] Nippon Shinyaku Co Ltd, Res Labs, Tsukuba, Ibaraki 3050003, Japan
关键词
sphingosine; 1-phosphate; mesangial cells; cDNA microarray; gene expression; calcium mobilization;
D O I
10.1016/S0006-291X(02)02850-4
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
Sphingosine 1-phosphate (S1P) is known to regulate cell proliferation, apoptosis, and motility. Recently, we have reported that SIP and its analogue dihydro-SIP (DHS1P) promote proliferation of rat cultured mesangial cells. To investigate the signaling mechanisms underlying S1P- and DHS1P-induced mesangial cell proliferation, we performed cDNA microarray analysis of gene expression during mesangial cell proliferation. In terms of the overall pattern, gene expression waves induced by SIP and DHS1P were similar to those induced by a potent mesangial mitogen platelet-derived growth factor (PDGF), whereas we found several genes, such as two growth factors, connective tissue growth factor (CTGF) and heparin-binding EGF-like growth factor (HB-EGF), which were induced by the sphingolipids, but not by PDGF. Cluster analysis also identified calcium-dependent molecules highly expressed in DHS1P-stimulated cells compared to SIP-stimulated cells. Calcium mobilization analysis showed that DHS1P had higher magnitudes of intracellular calcium mobilization than S1P, suggesting that S1P and DHS1P differentially regulate intracellular calcium mobilization, possibly leading to different gene expression in mesangial cells. The large-scale monitoring of gene expression performed here allows us to identify SIP-induced transcriptional properties during mesangial cell proliferation. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:577 / 584
页数:8
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