C/EBPβ and C/EBPδ transcription factors: Basic biology and roles in the CNS

被引:84
|
作者
Pulido-Salgado, Marta [1 ]
Vidal-Taboada, Jose M. [1 ]
Saura, Josep [1 ]
机构
[1] Univ Barcelona, IDIBAPS, Sch Med, Biochem & Mol Biol Unit, E-08036 Barcelona, Spain
关键词
CCAAT/enhancer binding protein; Transcription factor; Neuron; Microglia; Astrocyte; Neuroinflammation; BINDING-PROTEIN-BETA; NITRIC-OXIDE SYNTHASE; MAMMARY EPITHELIAL-CELLS; INFLAMMATORY CYTOKINE PRODUCTION; ENDOPLASMIC-RETICULUM STRESS; NUCLEAR FACTOR INTERLEUKIN-6; PROSTAGLANDIN E-2 PRODUCTION; MITOTIC CLONAL EXPANSION; BRAIN GENOMIC RESPONSE; LONG-TERM FACILITATION;
D O I
10.1016/j.pneurobio.2015.06.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
CCAAT/enhancer binding protein (C/EBP) beta and C/EBP delta are transcription factors of the basic-leucine zipper class which share phylogenetic, structural and functional features. In this review we first describe in depth their basic molecular biology which includes fascinating aspects such as the regulated use of alternative initiation codons in the C/EBP beta mRNA. The physical interactions with multiple transcription factors which greatly opens the number of potentially regulated genes or the presence of at least five different types of post-translational modifications are also remarkable molecular mechanisms that modulate C/EBP beta and C/EBP delta function. In the second part, we review the present knowledge on the localization, expression changes and physiological roles of C/EBP beta and C/EBP delta in neurons, astrocytes and microglia. We conclude that C/EBP beta and C/EBP delta share two unique features related to their role in the CNS: whereas in neurons they participate in memory formation and synaptic plasticity, in glial cells they regulate the pro-inflammatory program. Because of their role in neuroinflammation, C/EBP beta and C/EBP delta in microglia are potential targets for treatment of neurodegenerative disorders. Any strategy to reduce C/EBP beta and C/EBP delta activity in neuroinflammation needs to take into account its potential side-effects in neurons. Therefore, cell-specific treatments will be required for the successful application of this strategy. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 33
页数:33
相关论文
共 50 条
  • [31] C/EBP family transcription factors are degraded by the proteasome but stabilized by forming dimer
    Takayuki Hattori
    Nobumichi Ohoka
    Yasumichi Inoue
    Hidetoshi Hayashi
    Kikuo Onozaki
    Oncogene, 2003, 22 : 1273 - 1280
  • [32] Altered myeloid differentiation with impaired function of C/EBP transcription factors.
    Iwama, A
    Osawa, M
    Kaneko, S
    Onodera, M
    Vinson, C
    Tenen, DG
    Nakauchi, H
    BLOOD, 2000, 96 (11) : 668A - 668A
  • [33] Keratinocyte growth factor and the transcription factors C/EBPα, C/EBPβ, and SREBP-1c regulate fatty acid synthesis in alveolar type II cells
    Mason, RJ
    Pan, TL
    Edeen, KE
    Nielsen, LD
    Zhang, FJ
    Longphre, M
    Eckart, MR
    Neben, S
    JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (02): : 244 - 255
  • [34] The Natural Product Betulinic Acid Inhibits C/EBP Family Transcription Factors
    Hollis, Angela
    Sperl, Bianca
    Graeber, Martin
    Berg, Thorsten
    CHEMBIOCHEM, 2012, 13 (02) : 302 - 307
  • [35] Interaction and functional interference of C/EBPβ with octamer factors in immunoglobulin gene transcription
    Hatada, EN
    Chen-Kiang, S
    Scheidereit, C
    EUROPEAN JOURNAL OF IMMUNOLOGY, 2000, 30 (01) : 174 - 184
  • [36] Regulation of senescence and the SASP by the transcription factor C/EBPβ
    Salotti, Jacqueline
    Johnson, Peter F.
    EXPERIMENTAL GERONTOLOGY, 2019, 128
  • [37] CREB controls LAP/C/EBP beta transcription
    Niehof, M
    Manns, MP
    Trautwein, C
    MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (07) : 3600 - 3613
  • [38] The transcription factor C/EBPα in lung development and cancer
    Levantini, Elena
    Basseres, Daniela S.
    Ji, Hongbin
    Monti, Stefano
    Kim, Carla Bender
    Elf, Shannon
    Hetherington, Christopher
    Kocher, Olivier
    Golub, Todd
    Jacks, Tyler
    Wong, Kwok-Kin
    Halmos, Balazs
    Tenen, Daniel G.
    CANCER RESEARCH, 2006, 66 (08)
  • [39] The transcription factor C/EBPα isoform p30 promotes osteoblastogenesis but inhibits adipogenesis contrary to C/EBPα
    Ueda, M
    Hata, K
    Ikeda, F
    Matsubara, T
    Ebisu, S
    Nishimura, R
    Yoneda, T
    JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 : S78 - S78
  • [40] SELECTIVE MICROGLIAL DEPLETION OF THE TRANSCRIPTION FACTOR C/EBPβ IN LYSM-CRE/C/EBPβFL/FL MICE
    Pulido-Salgado, M.
    Valente, T.
    Straccia, M.
    Tusell, J. M.
    Sola, C.
    Saura, J.
    GLIA, 2013, 61 : S93 - S93