Polysialic acid and activity-dependent synapse remodeling

被引:48
|
作者
Bonfanti, Luca [2 ]
Theodosis, Dionysia T. [1 ]
机构
[1] Univ Bordeaux, INSERM, Neuroctr Magendie, U862, F-33077 Bordeaux, France
[2] Univ Turin, INN, NIT, Dept Vet Morphophysiol, Turin, Italy
关键词
adhesion; synaptic plasticity; astrocytes; central nervous system; hypothalamus; olfactory system; CELL-ADHESION MOLECULE; HIGHLY SIALYLATED ISOFORM; ACCESSORY OLFACTORY-BULB; ADULT-RAT; PSA-NCAM; TRANSIENT INCREASES; NEURONAL PRECURSORS; PIRIFORM CORTEX; GENERATED CELLS; MICE DEFICIENT;
D O I
10.4161/cam.3.1.7258
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Polysialic acid (PSA) is a large carbohydrate added post-translationally to the extracellular domain of the Neural Cell Adhesion Molecule (NCAM) that influences its adhesive and other functional properties. PSA-NCAM is widely distributed in the developing nervous system where it promotes dynamic cell interactions, like those responsible for axonal growth, terminal sprouting and target innervation. Its expression becomes restricted in the adult nervous system where it is thought to contribute to various forms of neuronal and glial plasticity. We here review evidence, obtained mainly from hypothalamic neuroendocrine centers and the olfactory system, that it intervenes in structural synaptic plasticity and accompanying neuronal-glial transformations, making possible the formation and elimination of synapses that occur under particular physiological conditions. While the mechanism of action of this complex sugar is unknown, it is now clear that it is a necessary molecular component of various cell transformations, including those responsible for activity-dependent synaptic remodeling.
引用
收藏
页码:43 / 50
页数:8
相关论文
共 50 条
  • [21] Cell surface expression of polysialic acid on NCAM is a prerequisite for activity-dependent morphological neuronal and glial plasticity
    Theodosis, DT
    Bonhomme, R
    Vitiello, S
    Rougon, G
    Poulain, DA
    JOURNAL OF NEUROSCIENCE, 1999, 19 (23): : 10228 - 10236
  • [22] Presynaptic remodeling contributes to activity-dependent synaptogenesis
    Nikonenko, I
    Jourdain, P
    Muller, D
    JOURNAL OF NEUROSCIENCE, 2003, 23 (24): : 8498 - 8505
  • [23] The molecular signals that regulate activity-dependent synapse refinement in the brain
    Nagappan-Chettiar, Sivapratha
    Yasuda, Masahiro
    Johnson-Venkatesh, Erin M.
    Umemori, Hisashi
    CURRENT OPINION IN NEUROBIOLOGY, 2023, 79
  • [24] ACTIVITY-DEPENDENT DEVELOPMENT OF THE NEUROMUSCULAR SYNAPSE DURING DROSOPHILA EMBRYOGENESIS
    BROADIE, K
    BATE, M
    NEURON, 1993, 11 (04) : 607 - 619
  • [25] Activity-dependent synapse validation by neurexin ligands, LRRTMs and neuroligins
    Ko, Jaewon
    Sudhof, Thomas C.
    NEUROSCIENCE RESEARCH, 2011, 71 : E17 - E18
  • [26] Activity-dependent modulation of synapse-regulating genes in astrocytes
    Farhy-Tselnicker, Isabella
    Boisvert, Matthew M.
    Liu, Hanqing
    Dowling, Cari
    Erikson, Galina A.
    Blanco-Suarez, Elena
    Farhy, Chen
    Shokhirev, Maxim N.
    Ecker, Joseph R.
    Allen, Nicola J.
    ELIFE, 2021, 10
  • [27] Activity-dependent long-term depression and synapse silencing
    Hagler, DJ
    Goda, Y
    JOURNAL OF NEUROCHEMISTRY, 1999, 73 : S4 - S4
  • [28] SYNAPSE ELIMINATION BY TRANSPLANTED ASTROCYTES IN CEREBELLAR CULTURES IS NOT ACTIVITY-DEPENDENT
    SEIL, FJ
    EXPERIMENTAL NEUROLOGY, 1995, 135 (02) : 169 - 169
  • [29] Critical period for activity-dependent synapse elimination in developing cerebellum
    Kakizawa, S
    Yamasaki, M
    Watanabe, M
    Kano, M
    JOURNAL OF NEUROSCIENCE, 2000, 20 (13): : 4954 - 4961
  • [30] Retrograde BMP Signaling at the Synapse: A Permissive Signal for Synapse Maturation and Activity-Dependent Plasticity
    Berke, Brett
    Wittnam, Jessica
    McNeill, Elizabeth
    Van Vactor, David L.
    Keshishian, Haig
    JOURNAL OF NEUROSCIENCE, 2013, 33 (45): : 17937 - 17950