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Biological roles of CCAAT/Enhancer-binding protein delta during inflammation
被引:97
|作者:
Ko, Chiung-Yuan
[1
,2
]
Chang, Wen-Chang
[3
]
Wang, Ju-Ming
[3
,4
,5
,6
]
机构:
[1] Taipei Med Univ, Coll Med Sci & Technol, Program Neural Regenerat Med, Taipei 11031, Taiwan
[2] Taipei Med Univ, Ctr Neurotrauma & Neuroregenerat, Taipei 11031, Taiwan
[3] Taipei Med Univ, Grad Inst Med Sci, Coll Med, Taipei 11031, Taiwan
[4] Natl Cheng Kung Univ, Inst Bioinformat & Biosignal Transduct, Coll Biosci & Biotechnol, Tainan 70101, Taiwan
[5] Natl Cheng Kung Univ, Infect Dis & Signaling Res Ctr, Tainan 70101, Taiwan
[6] Natl Cheng Kung Univ, Ctr Mol Inflammat, Tainan 70101, Taiwan
关键词:
TRAUMATIC BRAIN-INJURY;
NITRIC-OXIDE SYNTHASE;
ACUTE-PHASE RESPONSE;
ACUTE LUNG INJURY;
3 C/EBP ISOFORMS;
NF-KAPPA-B;
TRANSCRIPTION FACTORS;
GENE-EXPRESSION;
ADIPOCYTE DIFFERENTIATION;
CYCLOOXYGENASE-2;
GENE;
D O I:
10.1186/s12929-014-0110-2
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
CCAAT/enhancer-binding protein delta (CEBPD) belongs to the CCAAT/enhancer-binding protein family, and these proteins function as transcription factors in many biological processes, including cell differentiation, motility, growth arrest, proliferation, cell death, metabolism and immune responses. The functional diversity of CEBPD depends, in part, on the cell type and cellular context, which indicates that CEBPD could interpret a variety of cues to adjust cellular responses in specific situations. Here, we review the regulation of the CEBPD gene and its function in response to inflammatory stimuli. We also address its effects in inflammation-related diseases through a discussion of its recently discovered downstream targets. Regarding to the previous discoveries and new insights in inflammation-associated diseases, suggesting CEBPD could also be a central gene in inflammation. Importantly, the results of this study indicate that the investigation of CEBPD could open a new avenue to help better understand the inflammatory response.
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页数:8
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