EphA/ephrin-A signaling is critically involved in region-specific apoptosis during early brain development

被引:35
|
作者
Park, E. [1 ]
Kim, Y. [1 ]
Noh, H. [1 ]
Lee, H. [1 ]
Yoo, S. [1 ]
Park, S. [1 ]
机构
[1] Sookmyung Womens Univ, Dept Biol Sci, Seoul 140742, South Korea
来源
CELL DEATH AND DIFFERENTIATION | 2013年 / 20卷 / 01期
基金
新加坡国家研究基金会;
关键词
EphA; ephrin-A; apoptosis; early brain development; PROGRAMMED CELL-DEATH; NERVOUS-SYSTEM DEVELOPMENT; RECEPTOR TYROSINE KINASES; NEURAL-TUBE CLOSURE; EPH RECEPTORS; DECREASED APOPTOSIS; AXON REPULSION; CASPASE; 9; IN-VIVO; EPHRINS;
D O I
10.1038/cdd.2012.121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
EphAs and ephrin-As have been implicated in the morphogenesis of the developing brain. We found that EphA7 and ephrin-A5 are coexpressed in the dorsal midline (DM) of the diencephalon and anterior mesencephalon. Interestingly, programmed cell death (PCD) of the neural epithelial cells normally found in this region was reduced in ephrin-A5/ephrin-A2 dual-deficient embryos. In contrast, in vivo expression of ephrin-A5-Fc or full-length ephrin-A5 strongly induced apoptosis in neural epithelial cells and was accompanied by severe brain malformation during embryonic development. Expression of ephrinA5-Fc correlated with apoptosis of EphA7-expressing cells, whereas null mutation of ephrin-A5 resulted in the converse phenotype. Importantly, null mutation of caspase-3 or endogenous ephrin-A5 attenuated the PCD induced by ectopically overexpressed ephrin-A5. Together, our results suggest that brain region-specific PCD may occur in a region where EphAs cluster with neighboring ephrin-As through cell-cell contact. Cell Death and Differentiation (2013) 20, 169-180; doi:10.1038/cdd.2012.121; published online 14 September 2012
引用
收藏
页码:169 / 180
页数:12
相关论文
共 50 条
  • [31] Region-specific changes in brain kisspeptin receptor expression during estrogen depletion and the estrous cycle
    Ozaki, Saeko
    Higo, Shimpei
    Iwata, Kinuyo
    Saeki, Hidehisa
    Ozawa, Hitoshi
    HISTOCHEMISTRY AND CELL BIOLOGY, 2019, 152 (01) : 25 - 34
  • [32] Defining brain region-specific glucocorticoid action during stress by conditional gene disruption in mice
    Kolber, Benedict J.
    Muglia, Louis J.
    BRAIN RESEARCH, 2009, 1293 : 85 - 90
  • [33] Region-specific accumulation of oxidatively-induced DNA damage in brain during aging.
    Cardozo-Pelaez, F
    Song, S
    Parthasarathy, A
    Naidu, K
    Sanchez-Ramos, J
    JOURNAL OF NEUROCHEMISTRY, 1998, 70 : S25 - S25
  • [34] Region-specific changes in brain kisspeptin receptor expression during estrogen depletion and the estrous cycle
    Saeko Ozaki
    Shimpei Higo
    Kinuyo Iwata
    Hidehisa Saeki
    Hitoshi Ozawa
    Histochemistry and Cell Biology, 2019, 152 : 25 - 34
  • [35] Regulators of G-protein signaling (RGS) proteins: Region-specific expression of nine subtypes in rat brain
    Gold, SJ
    Ni, YG
    Dohlman, HG
    Nestler, EJ
    JOURNAL OF NEUROSCIENCE, 1997, 17 (20): : 8024 - 8037
  • [36] Brain Region-specific Changes in Extracellular Signal-regulated Kinase (ERK)-5 Signaling in Suicide Subjects
    Dwivedi, Yogesh
    Pandey, Ghanshyam
    Zhang, Hui
    NEUROPSYCHOPHARMACOLOGY, 2013, 38 : S324 - S324
  • [37] Dual function of the region-specific homeotic gene spalt during Drosophila tracheal system development
    Kuhnlein, RP
    Schuh, R
    DEVELOPMENT, 1996, 122 (07): : 2215 - 2223
  • [38] Development of a Region-Specific Physiologically Based Pharmacokinetic Brain Model to Assess Hippocampus and Frontal Cortex Pharmacokinetics
    Zakaria, Zaril
    Badhan, Raj
    PHARMACEUTICS, 2018, 10 (01):
  • [39] Region-specific decline in the expression of metabotropic glutamate receptor 7 mRNA in rat brain during aging
    Simonyi, A
    Miller, LA
    Sun, GY
    MOLECULAR BRAIN RESEARCH, 2000, 82 (1-2): : 101 - 106
  • [40] Early-Ethanol Exposure Induced Region-Specific Changes in Metabolic Proteins in the Rat Brain: A Proteomics Study
    Swart, Patricia C.
    Russell, Vivienne A.
    Vlok, Nicolaas M.
    Dimatelis, Jacqueline J.
    JOURNAL OF MOLECULAR NEUROSCIENCE, 2018, 65 (03) : 277 - 288