Apoptosis-Induced Gene Profiles of a Myeloma Cell P3-X63-Ag8.653.
- Author:
Hye Seung BAHNG
1
;
Yong Hoon CHUNG
Author Information
- Publication Type:Original Article
- Keywords: Myeloma; P3-X63-Ag8.653; apoptosis; GE-array; GeneChip analysis; Northern analysis; cytochrome c; caspase 9
- MeSH: Aminopterin; Animals; Apoptosis; Caspase 9; Cell Cycle; Cell Death; Cytochromes c; Homeostasis; Hypoxanthine Phosphoribosyltransferase; Immune System Diseases; Membranes; Mice; Mitochondria; Neurodegenerative Diseases; Transcription Factors
- From:Immune Network 2006;6(3):128-137
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Apoptosis is a physiologic phenomenon involved in development, elimination of damaged cells, and maintenance of cell homeostasis. Deregulation of apoptosis may cause diseases, such as cancers, immune diseases, and neurodegenerative disorders. The mouse myeloma cell P3-X63-Ag8.653 (v653) is an HGPRT deficient (HGPRT) mutant strain. High dependency on de novo transcription and translation of aminopterin induced apoptosis of this cell seems to be an ideal experimental system for searching apoptosis-induced genes. METHODS & RESULTS: For searching apoptosis-related genes we carried out GE-array (dot blot), Affymetrix GeneChip analysis, Northern analysis and differential display-PCR techniques. The chip data were analyzed with three different programs. 66 genes were selected through Affymetrix GeneChip analyses. All genes selected were classified into 8 groups according to their known functions. They were Genes of 1) Cell growth/maintenance/death/ enzyme, 2) Cell cycle, 3) Chaperone, 4) Cancer/disease-related genes, 5) Mitochondria, 6) Membrane protein/signal transduction, 7) Nuclear protein/nucleic acid binding/ transcription binding and 8) Translation factor. Among these groups number of genes were the largest in the genes of cell growth/maintenance/death/enzyme. Expression signals of most of all groups were peaked at 3 hour of apoptosis except genes of Nuclear protein/nucleic acid binding/ transcription factor which showed maximum signal at 1 hour. CONCLUSION: This study showed induction of wide range of proapoptotic factors which accelerate cell death at various stage of cell death. In addition apoptosis studied in this research can be classified as a type 2 which involves cytochrome c and caspase 9 especially in early stages of death. But It also has progressed to type 1 in late stage of the death process.
