Expression of reef coral fluorescent proteins in the central nervous system of transgenic mice

被引:124
作者
Hirrlinger, PG
Scheller, A
Braun, C
Quintela-Schneider, M
Fuss, B
Hirrlinger, J
Kirchhoff, F
机构
[1] Max Planck Inst Expt Med, Dept Neurogenet, D-37075 Gottingen, Germany
[2] Max Planck Inst Expt Med, Dept Mol Neurobiol, D-37075 Gottingen, Germany
[3] Virginia Commonwealth Univ, Dept Anat & Neurobiol, Richmond, VA 23284 USA
[4] DFG Res Ctr Mol Physiol Brain, CMPB, Gottingen, Germany
[5] Free Univ Berlin, Sect Biol Chem & Pharm, D-1000 Berlin, Germany
关键词
D O I
10.1016/j.mcn.2005.08.011
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Reef coral fluorescent proteins (RCFPs) are bright fluorescent proteins (FPs) covering a wide spectral range. We used various RCFP genes to transgenically color different cell populations in the brain. The mouse Thy1.2 promoter was used to target expression of HcRed1 in neurons, the human glial fibrillary acidic protein (GFAP) promoter to label astrocytes with AmCyan1, AsRed2 and mRFP1 as well as the mouse proteolipid protein promoter to mark oligodendrocytes with DsRed1. In brain sections of transgenic mice, RCFP expression was found to be highly specific using immunohistochemistry and fluorescence microscopy. In contrast to transgenic mice with expression of jellyfish FP variants, RCFPs formed numerous fluorescent precipitates. These aggregates were primarily found in cell somata and also in cell processes. Older mice were more affected than younger ones. Despite these fluorescent deposits, physiological properties of RCFP expressing brain cells such as whole-cell membrane currents or glutamate-evoked calcium signaling seemed to be unaffected. While brightness and spectral variation of RCFPs are optimal for expression in transgenic animals used in physiological experiments, the formation of fluorescent precipitates in various cell types limits their use for morphological cell analysis in situ. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:291 / 303
页数:13
相关论文
共 45 条
  • [1] Protein misfolding in neurodegenerative diseases
    Agorogiannis, EI
    Agorogiannis, GI
    Papadimitriou, A
    Hadjigeorgiou, GM
    [J]. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2004, 30 (03) : 215 - 224
  • [2] Postnatal NG2 proteoglycan-expressing progenitor cells are intrinsically multipotent and generate functional neurons
    Belachew, S
    Chittajallu, R
    Aguirre, AA
    Yuan, XQ
    Kirby, M
    Anderson, S
    Gallo, V
    [J]. JOURNAL OF CELL BIOLOGY, 2003, 161 (01) : 169 - 186
  • [3] BERGER T, 1991, J NEUROSCI, V11, P3008
  • [4] GFAP PROMOTER DIRECTS ASTROCYTE-SPECIFIC EXPRESSION IN TRANSGENIC MICE
    BRENNER, M
    KISSEBERTH, WC
    SU, Y
    BESNARD, F
    MESSING, A
    [J]. JOURNAL OF NEUROSCIENCE, 1994, 14 (03) : 1030 - 1037
  • [5] A monomeric red fluorescent protein
    Campbell, RE
    Tour, O
    Palmer, AE
    Steinbach, PA
    Baird, GS
    Zacharias, DA
    Tsien, RY
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) : 7877 - 7882
  • [6] Overexpression of growth-associated proteins in the neurons of adult transgenic mice
    Caroni, P
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 1997, 71 (01) : 3 - 9
  • [7] A THIN SLICE PREPARATION FOR PATCH CLAMP RECORDINGS FROM NEURONS OF THE MAMMALIAN CENTRAL NERVOUS-SYSTEM
    EDWARDS, FA
    KONNERTH, A
    SAKMANN, B
    TAKAHASHI, T
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1989, 414 (05): : 600 - 612
  • [8] Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP
    Feng, GP
    Mellor, RH
    Bernstein, M
    Keller-Peck, C
    Nguyen, QT
    Wallace, M
    Nerbonne, JM
    Lichtman, JW
    Sanes, JR
    [J]. NEURON, 2000, 28 (01) : 41 - 51
  • [9] Three-color imaging using fluorescent proteins in living zebrafish embryos
    Finley, KR
    Davidson, AE
    Ekker, SC
    [J]. BIOTECHNIQUES, 2001, 31 (01) : 66 - +
  • [10] Novel fluorescent protein from Discosoma coral and its mutants possesses a unique far-red fluorescence
    Fradkov, AF
    Chen, Y
    Ding, L
    Barsova, EV
    Matz, MV
    Lukyanov, SA
    [J]. FEBS LETTERS, 2000, 479 (03): : 127 - 130