Astroglial processes show spontaneous motility at active synaptic terminals in situ

被引:198
作者
Hirrlinger, J
Hülsmann, S
Kirchhoff, F
机构
[1] Max Planck Inst Expt Med, Dept Neurogenet, D-37075 Gottingen, Germany
[2] DFG Res Ctr Mol Physiol Brain, Gottingen, Germany
[3] Univ Gottingen, Dept Neuro & Sensory Physiol, D-3400 Gottingen, Germany
关键词
astrocyte; transgenic mice; green fluorescent protein; neuron-glia interaction; brainstem slice;
D O I
10.1111/j.1460-9568.2004.03689.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Within the tripartite structure of vertebrate synapses, enwrapping astroglial processes regulate synaptic transmission by transmitter uptake and by direct transmitter release. We applied confocal and two-photon laser scanning microscopy to acutely isolated slices prepared from the brainstem of transgenic TgN(GFAP-EGFP) mice. In transversal sections fluorescently labelled astrocytes are evenly distributed throughout the tissue. Astroglial processes contacted neuronal somata and enwrapped active synaptic terminals as visualized using FM1-43 staining in situ. Here, at these synaptic regions astroglial process endings displayed a high degree of dynamic morphological changes. Two defined modes of spontaneous motility could be distinguished: (i) gliding of thin lamellipodia-like membrane protrusions along neuronal surfaces and (ii) transient extensions of filopodia-like processes into the neuronal environment. Our observations highlight the active role of astrocytes in direct modulation of synaptic transmission.
引用
收藏
页码:2235 / 2239
页数:5
相关论文
共 30 条
  • [1] Aldskogius H, 1999, J NEUROSCI RES, V58, P33, DOI 10.1002/(SICI)1097-4547(19991001)58:1<33::AID-JNR5>3.3.CO
  • [2] 2-D
  • [3] Astrocytes contain a vesicular compartment that is competent for regulated exocytosis of glutamate
    Bezzi, P
    Gundersen, V
    Galbete, JL
    Seifert, G
    Steinhäuser, C
    Pilati, E
    Volterra, A
    [J]. NATURE NEUROSCIENCE, 2004, 7 (06) : 613 - 620
  • [4] GLUTAMATE TRANSPORTERS IN GLIAL PLASMA-MEMBRANES - HIGHLY DIFFERENTIATED LOCALIZATIONS REVEALED BY QUANTITATIVE ULTRASTRUCTURAL IMMUNOCYTOCHEMISTRY
    CHAUDHRY, FA
    LEHRE, KP
    CAMPAGNE, MV
    OTTERSEN, OP
    DANBOLT, NC
    STORMMATHISEN, J
    [J]. NEURON, 1995, 15 (03) : 711 - 720
  • [5] Monitoring secretory membrane with FM1-43 fluorescence
    Cochilla, AJ
    Angleson, JK
    Betz, WJ
    [J]. ANNUAL REVIEW OF NEUROSCIENCE, 1999, 22 : 1 - 10
  • [6] Glutamate uptake
    Danbolt, NC
    [J]. PROGRESS IN NEUROBIOLOGY, 2001, 65 (01) : 1 - 105
  • [7] ANATOMICAL AND FUNCTIONAL IMAGING OF NEURONS USING 2-PHOTON LASER-SCANNING MICROSCOPY
    DENK, W
    DELANEY, KR
    GELPERIN, A
    KLEINFELD, D
    STROWBRIDGE, BW
    TANK, DW
    YUSTE, R
    [J]. JOURNAL OF NEUROSCIENCE METHODS, 1994, 54 (02) : 151 - 162
  • [8] EDWARDS FA, 1992, METHOD ENZYMOL, V207, P208
  • [9] El Majdoubi M, 2000, BIOCHEM CELL BIOL, V78, P317
  • [10] Dendritic spine changes associated with hippocampal long-term synaptic plasticity
    Engert, F
    Bonhoeffer, T
    [J]. NATURE, 1999, 399 (6731) : 66 - 70