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用重组亮氨酸拉链(Yo)蛋白进行被动转移和主动免疫,试图建立副肿瘤性小脑变性的动物模型。

Passive transfer and active immunization with the recombinant leucine-zipper (Yo) protein as an attempt to establish an animal model of paraneoplastic cerebellar degeneration.

作者信息

Tanaka K, Tanaka M, Onodera O, Igarashi S, Miyatake T, Tsuji S

机构信息

Department of Neurology, Niigata University, Japan.

出版信息

J Neurol Sci. 1994 Dec 20;127(2):153-8. doi: 10.1016/0022-510x(94)90067-1.

Abstract

Passive transfer of paraneoplastic cerebellar degeneration (PCD) IgG to rodents as well as active immunization with recombinant Yo fusion protein were tried in order to examine the roles of anti-Purkinje cell antibody (anti-Yo antibody) present in the sera and cerebrospinal fluid of patients with PCD in Purkinje cell loss, the hall mark of PCD pathology. On a single injection of PCD IgG to mouse brain, IgG was taken into Purkinje cells and remained there for more than 36 h without Purkinje cell loss. Injection of PCD IgG together with complement or lipopolysaccharide-activated human macrophages or rat mononuclear cells to rats ventricles did not cause Purkinje cell loss. We made a recombinant Yo fusion protein that has the leucine-zipper protein (Yo protein), the common epitope for anti-Yo antibody. Mice immunized with this Yo protein produced high titer antibody against it for more than 3 months, during which time neither neurological symptoms nor Purkinje cell loss occurred. The anti-Yo antibody, with or without complement or activated mononuclear cells, therefore could not be the sole cause of Purkinje cell loss.

摘要

为了研究副肿瘤性小脑变性(PCD)患者血清和脑脊液中存在的抗浦肯野细胞抗体(抗Yo抗体)在PCD病理学标志性特征——浦肯野细胞丢失中所起的作用,尝试将PCD IgG被动转移至啮齿动物体内,并对其用重组Yo融合蛋白进行主动免疫。向小鼠脑内单次注射PCD IgG后,IgG被摄取到浦肯野细胞中,并在那里停留超过36小时,而没有浦肯野细胞丢失。将PCD IgG与补体或脂多糖激活的人巨噬细胞或大鼠单核细胞一起注射到大鼠脑室中,并未导致浦肯野细胞丢失。我们制备了一种具有亮氨酸拉链蛋白(Yo蛋白)的重组Yo融合蛋白,Yo蛋白是抗Yo抗体的共同表位。用这种Yo蛋白免疫的小鼠产生了针对它的高滴度抗体,持续超过3个月,在此期间既没有出现神经症状,也没有浦肯野细胞丢失。因此,抗Yo抗体,无论有无补体或活化的单核细胞,都不可能是浦肯野细胞丢失的唯一原因。

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