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Zhongguo zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine / Zhongguo Zhong xi yi jie he xue hui, Zhongguo Zhong yi yan jiu yuan zhu ban 2007-Nov

[Experimental study of hematopoietic cell gene expression profile induced by panax notoginosides in vitro].

Vetëm përdoruesit e regjistruar mund të përkthejnë artikuj
Identifikohuni Regjistrohu
Lidhja ruhet në kujtesën e fragmenteve
Rui-lan Gao
Xiao-jie Lin
Xiao-hong Chen

Fjalë kyçe

Abstrakt

OBJECTIVE

To explore the relationship of up-regulated genes with cell proliferation and differentiation by analyzing the hematopoietic cells gene expression profile induced by panax notoginosides (PNS) using cDNA microarray.

METHODS

The cDNA membrane microarray with 480 target genes related to proliferation and differentiation of hematopoietic cells was prepared, and mRNA was extracted and purified from 3 lineages of human hematopoietic cell lines, including megakaryocytic CHRF-288, granulocytic HL-60 and erythrocytic K562 cells, respectively after they were treated with PNS. The hybridization with target genes on microarray membrane was performed using [alpha-33 ]dATP labeled cDNA from reversed mRNA.

RESULTS

After treated by PNS, the genes up-regulated for more than 3 folds could be classified to 11 sorts according to their function, including the methyl-transferase, acetyl-transferase, differentiation initiated factor, anti-apoptosis, transcription regulation protein, cell cycle related protein, protein and kinase of signal pathway, receptors, DNA or RNA polymerase, protein phosphatase, transporter or trafficking protein and rat sarcoma (RAS) homology gene family. In three cell lines of CHRF-288, HL-60 and K562 treated by PNS, 78 (16.3%), 89 (18.5%) and 59 (12.3%) pieces of genes respectively were up-regulated for more than 3 folds.

CONCLUSIONS

All the up-regulated genes induced by PNS in microarray analysis were related to hematopoietic cell proliferation and differentiation, the outcome is in accord with the results reported previously by the authors from the studies of mice model with hematopathy, hematopoietic stem/progenitor cells, gene transcription regulation and protein kinase of signal pathway, etc. It provides a powerful evidence for the PNS activity and its mechanism by gene expression profile.

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