Isoform pattern of 14-3-3 proteins in the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease

被引:92
作者
Wiltfang, J
Otto, M
Baxter, HC
Bodemer, M
Steinacker, P
Bahn, E
Zerr, I
Kornhuber, J
Kretzschmar, HA
Poser, S
Rüther, E
Aitken, A
机构
[1] Univ Gottingen, Dept Psychiat, Neurobiol Lab, D-37075 Gottingen, Germany
[2] Univ Gottingen, Dept Neurol, D-37075 Gottingen, Germany
[3] Univ Gottingen, Dept Neuropathol, D-37075 Gottingen, Germany
[4] Univ Edinburgh, Dept Biomed Sci Biochem, Edinburgh, Midlothian, Scotland
关键词
Creutzfeldt-Jakob disease; cerebrospinal fluid; 14-3-3; proteins; isoform-specific antibodies; Alzheimer's disease;
D O I
10.1046/j.1471-4159.1999.0732485.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Two-dimensional polyacrylamide gel electrophoresis of CSF has been used in the diagnosis of Creutzfeldt-Jakob disease (CJD). One of the two diagnostic protein spots was identified as isoform(s) of the 14-3-3 family of abundant brain proteins. This has led to the development of one-dimensional 14-3-3 sodium dodecyl sulfate polyacrylamide gel electrophoresis immunoblot, which is currently used to support the diagnosis of CJD. In the present study employing western blot analysis, we have identified the panel of 14-3-3 isoforms that appear in the CSF of 10 patients with CJD compared with 10 patients with other dementias. The results clearly show that the 14-3-3 isoforms beta, gamma, epsilon, and eta are present in the CSF of patients with CJD and can be used to differentiate other dementias. 14-3-3 eta also gave a baseline signal in all patients with other dementias, including six patients with Alzheimer's disease. The presence of 14-3-3 eta in the CSF of a patient with herpes simplex encephalitis was particularly noteworthy. This study has determined that isoform-specific 14-3-3 antibodies against beta, gamma, and epsilon should be considered for the neurochemical differentiation of CJD from other neurodegenerative diseases.
引用
收藏
页码:2485 / 2490
页数:6
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