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使用特定培养系统研究中期因子对胚胎小脑神经元的新型神经元效应。

Novel neuronal effects of midkine on embryonic cerebellar neurons examined using a defined culture system.

作者信息

Matsuzawa M, Muramatsu T, Yamamori T, Knoll W, Yano R

机构信息

Lab for Exotic Nanomaterials, RIKEN, Saitama, Japan.

出版信息

Cell Mol Neurobiol. 1999 Apr;19(2):209-21. doi: 10.1023/a:1006925110584.

Abstract
  1. Midkine (MK) is known to be a member of a family of heparin-binding neurotrophic factors. We used a chemically defined culture system to examine neuronal activities of MK on embryonic rat cerebellar cells. 2. In the culture system, a substrate surface was chemically modified either with amine or with laminin peptide to homogenize substrate conditions for culturing neurons. 3. At the optimal concentration (2.5 ng/ml), MK moderately promoted survivability (1.3-fold) and accelerated neurite outgrowth (1.4-fold) of cerebellar cells, putatively granule neurons, grown on an amine-modified surface. 4. Higher dosages (10 ng/ml or more) of MK, however, caused cellular fragmentation and detachment. Such degenerative effects were diminished by increasing the surface adhesiveness using laminin peptide, suggesting that the cellular degeneration might be caused by changes in the adhesive property of the neuron. 5. Using this culture system, we have found that MK has a novel modulatory activity of neuronal adhesiveness on the cultured cerebellar granule cells. Together with the expression pattern of MK, our study supports the idea that MK may be involved in the developmental events of the cerebellum.
摘要
  1. 中期因子(MK)是肝素结合神经营养因子家族的成员之一。我们使用化学限定培养系统来检测MK对胚胎大鼠小脑细胞的神经元活性。2. 在该培养系统中,底物表面用胺或层粘连蛋白肽进行化学修饰,以使培养神经元的底物条件均匀化。3. 在最佳浓度(2.5 ng/ml)下,MK适度促进了在胺修饰表面上生长的小脑细胞(推测为颗粒神经元)的存活能力(1.3倍)并加速了神经突生长(1.4倍)。4. 然而,更高剂量(10 ng/ml或更高)的MK会导致细胞破碎和脱离。通过使用层粘连蛋白肽增加表面粘附性,这种退化效应会减弱,这表明细胞退化可能是由神经元粘附特性的变化引起的。5. 使用这种培养系统,我们发现MK对培养的小脑颗粒细胞具有神经元粘附的新型调节活性。结合MK的表达模式,我们的研究支持MK可能参与小脑发育事件的观点。

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