Does ceruloplasmin differential express in the brain of Ts65Dn: a mouse mode of Down syndrome?

被引:0
|
作者
Yu, Bin [1 ,2 ]
Kong, Jing [1 ]
Xing, Baoling [2 ]
Zhu, Ziqiang [2 ]
Zhang, Bin [2 ]
Wang, Qiu-wei [2 ]
Shao, Shi-he [1 ]
机构
[1] Jiangsu Univ, Dept Microbiol, Sch Med Sci & Lab Med, Zhenjiang City 213003, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Changzhou Woman & Children Hlth Hosp, Changzhou City 213003, Jiangsu, Peoples R China
关键词
Down syndrome; Ceruloplasmin; Ts65Dn; Nervous system; ALZHEIMERS-DISEASE; DEMENTIA; COPPER;
D O I
10.1007/s10072-013-1570-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To investigate the expression of CP in Down syndrome (DS) mouse model, we especially observed the changes in neuronal CP. We systematically analyzed the level of CP in Ts65Dn mouse, including serum CP concentration and enzymatic activity, CP mRNA in brain, the expression of CP protein in brain. The applied technologies were ELISA, chemical colorimetry, RT-PCR, immunohistochemistry. Compared with the control group, there were no differences of significance in the concentration, enzymatic activity and unit activity of serum ceruloplasmin. By RT-PCR, we also found there were no significant differences in the level of CP mRNA. The expression of CP was positive in the endochylema of neuronal cells of both the groups, and there were no significant difference between the two groups. Meanwhile, there were no differences in four regions of the brain (cerebral cortex, hippocampus, thalamus and cerebella). Although the neurotoxic effects of CP related to some neurodegenerative diseases, but whether it does so in DS remains to be determined.
引用
收藏
页码:589 / 593
页数:5
相关论文
共 50 条
  • [41] APP accumulation and inflammation in the Ts65dn mouse, a model for Down's syndrome
    Lockrow, J
    Willis, L
    Granholm, AC
    Sambamurti, K
    EXPERIMENTAL NEUROLOGY, 2006, 198 (02) : 578 - 578
  • [42] Postnatal lethality and cardiac anomalies in the Ts65Dn Down Syndrome mouse model
    Moore, Clara S.
    MAMMALIAN GENOME, 2006, 17 (10) : 1005 - 1012
  • [43] Increased incidence of intermittent hypoxemia in the Ts65Dn mouse model of Down syndrome
    Das, Devsmita
    Medina, Brian
    Baktir, Mehmet Akif
    Mojabi, Fatemeh S.
    Fahimi, Atoossa
    Ponnusamy, Ravikumar
    Salehi, Ahmad
    NEUROSCIENCE LETTERS, 2015, 604 : 91 - 96
  • [44] Cognitive and pharmacological insights from the Ts65Dn mouse model of Down syndrome
    Ruparelia, Aarti
    Pearn, Matthew L.
    Mobley, William C.
    CURRENT OPINION IN NEUROBIOLOGY, 2012, 22 (05) : 880 - 886
  • [45] Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
    Laura G. Reinholdt
    Yueming Ding
    Griffith T. Gilbert
    Anne Czechanski
    Jeffrey P. Solzak
    Randall J. Roper
    Mark T. Johnson
    Leah Rae Donahue
    Cathleen Lutz
    Muriel T. Davisson
    Mammalian Genome, 2011, 22 : 685 - 691
  • [46] Molecular characterization of the translocation breakpoints in the Down syndrome mouse model Ts65Dn
    Reinholdt, Laura G.
    Ding, Yueming
    Gilbert, Griffith T.
    Czechanski, Anne
    Solzak, Jeffrey P.
    Roper, Randall J.
    Johnson, Mark T.
    Donahue, Leah Rae
    Lutz, Cathleen
    Davisson, Muriel T.
    MAMMALIAN GENOME, 2011, 22 (11-12) : 685 - 691
  • [47] Increased expression of β-catenin in brain microvessels of a segmentally trisomic (Ts65Dn) mouse model of Down syndrome
    Vorbrodt, Andrzej W.
    Li, Shuyun
    Brown, W. Ted
    Ramakrishna, Narayan
    BRAIN CELL BIOLOGY, 2008, 36 (5-6) : 203 - 211
  • [48] Neurochemical and cytochemical features in the brain of Ts65Dn mice: A model of Down syndrome
    Dierssen, M
    Megias, M
    Vallina, IF
    Baamonde, C
    Lumbreras, MA
    MartinezCue, C
    Calatayud, SG
    Escorihuela, RM
    FernandezTeruel, A
    Tobena, A
    Crespo, D
    Florez, J
    CYTOGENETICS AND CELL GENETICS, 1997, 77 : 29 - 29
  • [49] Subicular hypotrophy in fetuses with Down syndrome and in the Ts65Dn model of Down syndrome
    Stagni, Fiorenza
    Giacomini, Andrea
    Emili, Marco
    Uguagliati, Beatrice
    Bonasoni, Maria Paola
    Bartesaghi, Renata
    Guidi, Sandra
    BRAIN PATHOLOGY, 2019, 29 (03) : 366 - 379
  • [50] Regional increase in brain accumulation of myo-inositol in Ts65Dn mouse (Down syndrome model)
    Shetty, HU
    Siarey, RJ
    Stoll, J
    Galdzicki, Z
    Rapoport, SI
    JOURNAL OF NEUROCHEMISTRY, 1997, 69 : S30 - S30