Animal cells and systems

The Korean Society for Integrative Biology (한국통합생물학회)
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Microarray Study of Genes Differentially Modulated in Response to Nitric Oxide in Macrophages

  • Nan, Xuehua (Department of Biology, Institute of Bioscience and Biotechnology, Chungnam National University) ;
  • Maeng, Oky (Department of Biology, Institute of Bioscience and Biotechnology, Chungnam National University) ;
  • Shin, Hyo-Jung (Department of Biology, Institute of Bioscience and Biotechnology, Chungnam National University) ;
  • An, Hyun-Jung (Department of Biology, Institute of Bioscience and Biotechnology, Chungnam National University) ;
  • Yeom, Young-Il (Korea Research Institute of Bioscience and Biotechnology) ;
  • Lee, Hay-Young (Department of Biology, Institute of Bioscience and Biotechnology, Chungnam National University) ;
  • Paik, Sang-Gi (Department of Biology, Institute of Bioscience and Biotechnology, Chungnam National University)
  • Published : 2008.03.31
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Abstract

Nitric oxide(NO) has been known to play important roles in numerous physiologic processes including neurotransmission, vasorelaxation, and cellular apoptosis. Using a mouse cDNA gene chip, we examined expression patterns and time course of NO-dependent genes in mouse macrophage RAW264.7 cells. Genes shown to be upregulated more than two fold or at least at two serial time points were further selected and validated by RT-PCR. Finally, 81 selected genes were classified by function as signaling, apoptosis, inflammation, transcription, translation, ionic homeostasis and metabolism. Among those, genes related with signaling, apoptosis and inflammation, such as guanylate cyclase 1, soluble, alpha3(Gucy1a3); protein kinase C, alpha($Pkc{\alpha}$); lymphocyte protein tyrosine kinase(Lck); BCL2/adenovirus E1B 19 kDa-interacting protein(Bnip3); apoptotic protease activating factor 1(Apaf1); X-linked inhibitor of apoptosis(Xiap); cyclin G1(Ccng1); chemokine(C-C motif) ligand 4(Ccl4); B cell translocation gene 2, anti-proliferative(Btg2); lysozyme 2(Lyz2); secreted phosphoprotein 1(Spp1); heme oxygenase(decycling) 1(Hmox1); CD14 antigen(Cd14); and granulin(Grn) may play important roles in NO-dependent responses in murine macrophages.

Keywords

References

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