Gene Expression Profiling of SH-SY5Y Human Neuroblastoma Cells Treated with Ginsenoside Rg1 and Rb1

Ginsenoside Rg1 및 Rb1을 처리한 신경세포주(SH-SY5Y세포)의 유전자 발현양상

  • Lee, Joon-Noh (Seoul National Hospital) ;
  • Yang, Byung-Hwan (Department of Neuropsychiatry, College of Medicine & The Mental Health Research Institute, Hanyang University) ;
  • Choi, Seung-Hak (Department of Neuropsychiatry, College of Medicine & The Mental Health Research Institute, Hanyang University) ;
  • Kim, Seok-Hyun (Department of Neuropsychiatry, College of Medicine & The Mental Health Research Institute, Hanyang University) ;
  • Chai, Young-Gyu (Division of Molecular and Life Science, College of Science, Hanyang University) ;
  • Jung, Kyoung-Hwa (Division of Molecular and Life Science, College of Science, Hanyang University) ;
  • Lee, Jun-Seok (Department of Psychiatry, College of Medicine, Kwandong University, Myongji Hospital) ;
  • Choi, Kang-Ju (KT & G Central Research Institute) ;
  • Kim, Young-Suk (KT & G Central Research Institute)
  • 이준노 (국립서울병원) ;
  • 양병환 (한양대학교 정신건강연구소 및 의과대학 신경정신과학교실) ;
  • 최승학 (한양대학교 정신건강연구소 및 의과대학 신경정신과학교실) ;
  • 김석현 (한양대학교 정신건강연구소 및 의과대학 신경정신과학교실) ;
  • 채영규 (한양대학교 자연과학대학 분자생명과학부) ;
  • 정경화 (한양대학교 자연과학대학 분자생명과학부) ;
  • 이준석 (관동대학교 의과대학 명지병원 정신과학교실) ;
  • 최강주 (KT & G 중앙연구소) ;
  • 김영숙 (KT & G 중앙연구소)
  • Published : 2005.05.31

Abstract

Objectives:The ginsenoside Rg1 and Rb1, the major components of ginseng saponin, have neurotrophic and neuroprotective effects including promotion of neuronal survival and proliferation, facilitation of learning and memory, and protection from ischemic injury and apoptosis. In this study, to investigate the molecular basis of the effects of ginsenoside on neuron, we analyzed gene expression profiling of SH-SY5Y human neuroblastoma cells treated with ginsenoside Rg1 or Rb1. Methods:SH-SY5Y cells were cultured and treated in triplicate with ginsenoside Rg1 or Rb1($80{\mu}M$, $40{\mu}M$, $20{\mu}M$). The proliferation rates of SH-SY5Y cells were determined by MTT assay and microscopic examination. We used a high density cDNA microarray chip that contained 8K human genes to analyze the gene expression profiles in SH-SY5Y cells. We analyzed using the Significance Analysis of Microarray(SAM) method for identifying genes on a microarray with statistically significant changes in expression. Results:Treatment of SH-SY5Y cells with $80{\mu}M$ ginsenoside Rg1 or Rb1 for 36h showed maximal proliferation compared with other concentrations or control. The results of the microarray experiment yielded 96 genes were upregulated(${\geq}$3 fold) in Rg1 treated cells and 40 genes were up-regulated(${\geq}$2 fold) in Rb1 treated cells. Treatment with ginsenoside Rg1 for 36h induced the expression of some genes associated with protein biosynthesis, regulation of transcription or translation, cell proliferation and growth, neurogenesis and differentiation, regulation of cell cycle, energy transport and others. Genes associated with neurogenesis and neuronal differentiation such as SCG10 and MLP increased in ginsenoside Rg1 treated cells, but such changes did not occur in Rb1-group. Conclusion:Our data provide novel insights into the gene mechanisms involved in possible role for ginsenoside Rg1 or Rb1 in mediating neuronal proliferation or cell viability, which can elicit distinct patterns of gene expression in neuronal cell line. Ginsenoside Rg1 have more broad and strong effects than ginsenoside Rb1 in gene expression and related cellular physiology. In addition, we suggest that SCG10 gene, which is known to be expressed in neuronal differentiation during development and neuronal regeneration during adulthood, may have a role in enhancement of activity dependent synaptic plasticity or cytoskeletal regulation following treatment of ginsenoside Rg1. Further, ginsenoside Rg1 may have a possible role in regeneration of injured neuron, promotion of memory, and prevention from aging or neuronal degeneration.

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