Vawter M P, Frye M A, Hemperly J J, VanderPutten D M, Usen N, Doherty P, Saffell J L, Issa F, Post R M, Wyatt R J, Freed W J
Cellular Neurobiology Branch, NIDA-IRP, Baltimore, MD 21224, USA.
J Psychiatr Res. 2000 Jan-Feb;34(1):25-34. doi: 10.1016/s0022-3956(99)00026-6.
Neural cell adhesion molecule (N-CAM) is a cell recognition molecule, four major isoforms (180, 140, 120, and 105-115 kDa) of which are present in brain. N-CAM has several roles in cellular organization and CNS development. Previously we have found an elevation in CSF N-CAM 120 kDa in the CSF of patients with schizophrenia, bipolar disorder, and depression. We now report an increase in the variable alternative spliced exon (VASE), a 10 amino acid sequence inserted into the fourth N-CAM domain, in the CSF of patients with schizophrenia, but not in bipolar disorder or depression. VASE-immunoreactive (VASE-ir) bands were measured in CSF from patients with schizophrenia (n = 14), bipolar disorder I (n = 7), bipolar disorder II (n = 9), unipolar depression (n = 17) and matched controls (n = 37) by Western immunoblotting. Three VASE-ir bands were distinguished in lumbar CSF corresponding to heavy (165 kDa), medium (155 kDa) and low (140 kDa) MW. A logarithmic transformation was applied to the VASE protein units and analyzed with a MANOVA. There was a 51% and 45% increase in VASE heavy (p = 0.0008) and medium (p = 0.04) MW protein, respectively, in patients with schizophrenia as compared with normal controls. Current neuroleptic treatment in patients with schizophrenia had no effect on CSF VASE concentrations. VASE concentration correlated significantly with behavioral ratings in patients with schizophrenia but not affective disorders. Thus, VASE immunoreactivity is increased in schizophrenia but not in affective disorders. These results provide further evidence of an abnormality of N-CAM protein in chronic schizophrenia and suggest differences between schizophrenia and affective disorders in regulation of N-CAM.
神经细胞黏附分子(N-CAM)是一种细胞识别分子,其四种主要异构体(180、140、120和105 - 115 kDa)存在于大脑中。N-CAM在细胞组织和中枢神经系统发育中具有多种作用。此前我们发现,精神分裂症、双相情感障碍和抑郁症患者的脑脊液中N-CAM 120 kDa水平升高。我们现在报告,精神分裂症患者的脑脊液中可变选择性剪接外显子(VASE,一个插入到N-CAM第四个结构域的10个氨基酸序列)增加,而双相情感障碍或抑郁症患者则没有。通过蛋白质免疫印迹法对精神分裂症患者(n = 14)、双相I型障碍患者(n = 7)、双相II型障碍患者(n = 9)、单相抑郁症患者(n = 17)以及匹配的对照组(n = 37)的脑脊液中的VASE免疫反应性(VASE-ir)条带进行了测量。在腰段脑脊液中区分出了三条VASE-ir条带,分别对应高分子量(165 kDa)、中等分子量(155 kDa)和低分子量(140 kDa)。对VASE蛋白单位进行对数转换,并采用多变量方差分析进行分析。与正常对照组相比,精神分裂症患者的VASE高分子量(p = 0.0008)和中等分子量(p = 0.04)蛋白分别增加了51%和45%。精神分裂症患者目前的抗精神病药物治疗对脑脊液中VASE浓度没有影响。VASE浓度与精神分裂症患者的行为评分显著相关,但与情感障碍患者无关。因此,精神分裂症患者的VASE免疫反应性增加,而情感障碍患者则没有。这些结果为慢性精神分裂症中N-CAM蛋白异常提供了进一步证据,并提示精神分裂症和情感障碍在N-CAM调节方面存在差异。