Jones L L, Kreutzberg G W, Raivich G
Department of Neuromorphology, Max Planck Institute of Psychiatry, Martinsried, Germany.
Eur J Neurosci. 1997 Sep;9(9):1854-63. doi: 10.1111/j.1460-9568.1997.tb00752.x.
CD44 is a cell adhesion molecule which plays an important role in cell movement and adhesion, e.g. in lymphocyte homing and tumour metastasis. Here we studied the expression of CD44 mRNA and protein immunoreactivity in the facial nucleus after nerve injury and during the ensuing regeneration. Transection of the facial nerve led to a strong up-regulation of CD44, peaking 4 days after injury on the motoneurons of the axotomized facial nucleus. Use of the polymerase chain reaction confirmed the de novo expression of CD44 and detected only the standard haematopoietic CD44 isoform. Western blotting also detected the 76 kDa protein subtype, in line with the predicted size of the haematopoietic CD44 variant. At the ultrastructural level, CD44 immunoreactivity was restricted to the surface of the neuronal perikarya, their dendrites and axons. It was not seen in the adjacent activated astrocytes, microglia or vascular endothelia. This study shows strong up-regulation of the cell adhesion molecule CD44 on the regenerating motoneurons in the axotomized facial nucleus. These data suggest that CD44 may play a role in neurite outgrowth, in synaptic stripping or in the adhesion of activated glial cells to the perikaryal surface of the axotomized motoneurons.
CD44是一种细胞黏附分子,在细胞运动和黏附中发挥重要作用,例如在淋巴细胞归巢和肿瘤转移过程中。在此,我们研究了神经损伤后及随后再生过程中面神经核内CD44 mRNA和蛋白免疫反应性的表达。面神经横断导致CD44强烈上调,在损伤后4天在轴突切断的面神经核运动神经元上达到峰值。聚合酶链反应的结果证实了CD44的从头表达,并且仅检测到标准造血CD44亚型。蛋白质印迹法也检测到了76 kDa的蛋白亚型,与造血CD44变体的预测大小一致。在超微结构水平上,CD44免疫反应性仅限于神经元胞体、其树突和轴突的表面。在相邻的活化星形胶质细胞、小胶质细胞或血管内皮细胞中未观察到。本研究表明,在轴突切断的面神经核中,再生的运动神经元上细胞黏附分子CD具有强烈上调。这些数据表明,CD44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 444可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长、突触剥离或活化的胶质细胞与轴突切断的运动神经元胞体表面的黏附中发挥作用。 44可能在神经突生长