RSC96 Schwann Cell Proliferation and Survival Induced by Dilong through PI3K/Akt Signaling Mediated by IGF-I
Author(s) -
YungMing Chang,
WuHsien Kuo,
TungYuan Lai,
Ying-Ting Shih,
FuuJen Tsai,
ChangHai Tsai,
Wen-Tong Shu,
Yingyu Chen,
Yueh-Sheng Chen,
WeiWen Kuo,
ChihYang Huang
Publication year - 2009
Publication title -
evidence-based complementary and alternative medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.552
H-Index - 90
eISSN - 1741-4288
pISSN - 1741-427X
DOI - 10.1093/ecam/nep216
Subject(s) - pi3k/akt/mtor pathway , protein kinase b , microbiology and biotechnology , small interfering rna , biology , cell growth , cell cycle , cyclin d1 , gene knockdown , kinase , phosphorylation , cancer research , signal transduction , cell , biochemistry , rna , apoptosis , gene
Schwann cell proliferation is critical for the regeneration of injured nerves. Dilongs are widely used in Chinese herbal medicine to remove stasis and stimulate wound-healing functions. Exactly how this Chinese herbal medicine promotes tissue survival remains unclear. The aim of the present study was to investigate the molecular mechanisms by which Dilong promote neuron regeneration. Our results show that treatment with extract of Dilong induces the phosphorylation of the insulin-like growth factor-I (IGF-I)-mediated phosphatidylinositol 3-kinase/serine-threonine kinase (PI3K/Akt) pathway, and activates protein expression of cell nuclear antigen (PCNA) in a time-dependent manner. Cell cycle analysis showed that G 1 transits into the S phase in 12–16 h, and S transits into the G 2 phase 20 h after exposure to earthworm extract. Strong expression of cyclin D1, cyclin E and cyclin A occurs in a time-dependent manner. Small interfering RNA (siRNA)-mediated knockdown of PI3K significantly reduced PI3K protein expression levels, resulting in Bcl 2 survival factor reduction and a marked blockage of G 1 to S transition in proliferating cells. These results demonstrate that Dilong promotes the proliferation and survival of RSC96 cells via IGF-I signaling. The mechanism is mainly dependent on the PI3K protein.
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