Expression of the Heparin-Binding Growth Factor Midkine in the Cerebrospinal Fluid of Patients with Neurological Disorders
-
- Yoshida Yoshihiro
- School of Health Sciences, Faculty of Medicine, Kagoshima University
-
- Ikematsu Shinya
- Meiji Cell Technology Center, Meiji Milk Products Co. Ltd.
-
- Muramatsu Hisako
- Department of Biochemistry, School of Medicine, Nagoya University
-
- Sakakima Harutoshi
- School of Health Sciences, Faculty of Medicine, Kagoshima University
-
- Mizuma Nobuhisa
- Department of Neurology, Faculty of Medicine, Kagoshima University
-
- Matsuda Fumiyo
- School of Health Sciences, Faculty of Medicine, Kagoshima University
-
- Sonoda Ken
- Kagoshima Medical Association Hospital
-
- Umehara Fujio
- Department of Neurology, Faculty of Medicine, Kagoshima University
-
- Ohkubo Ryuichi
- Department of Neurology, Faculty of Medicine, Kagoshima University
-
- Matsuura Eiji
- Department of Neurology, Faculty of Medicine, Kagoshima University
-
- Goto Masamichi
- Department of Pathology, Faculty of Medicine, Kagoshima University
-
- Osame Mitsuhiro
- Department of Neurology, Faculty of Medicine, Kagoshima University
-
- Muramatsu Takashi
- Department of Biochemistry, School of Medicine, Nagoya University
Search this article
Abstract
Objective This study was to clarify the roles of midkine (MK) in the brain.<br> Methods We determined cerebrospinal fluid MK levels in patients with neurological disorders by enzyme-linked immunoassay and immunostained autopsied brain samples in patients with meningitis.<br> Results MK levels were 0.37±0.21 ng/ml in controls (n=46, mean ± S.D.), 0.67±0.19 ng/ml in patients with cerebral infarction (n=8), 1.78±1.32 ng/ml in patients with meningitis (n=25; ANOVA and post-hoc Fisher's PLSD test, p<0.0001), 0.31±0.25 ng/ml in patients with human T-lymphotrophic virus type I-associated myelopathy/tropical spastic paraparesis (n=29), and 0.42±0.17 ng/ml in patients with amyotrophic lateral sclerosis (n=8). The regression equations were Y=0.005X+0.498 (Y, CSF MK level; X, cell number) and Y=0.007X+0.326 (Y, MK level; X, protein level) for all CSF samples. Autopsy brain samples from patients with meningitis expressed MK weakly in mononuclear cells on immunohistochemical examination. Western blot and polymerase chain reaction analyses showed that leukocytes were MK positive. CSF MK levels were not high in patients with cerebral infarction but were increased in patients with meningitis. CSF MK levels were high in normal controls, compared to those of other cytokines. MK was expressed in choroid plexus of normal brain and released there.<br> Conclusion Our findings suggested that MK may maintain normal adult brain as a neurotrophic factor, and that MK may be released from leucocytes in brain of patients with meningitis as an immunological mediator.<br>
Journal
-
- Internal Medicine
-
Internal Medicine 47 (2), 83-89, 2008
The Japanese Society of Internal Medicine
- Tweet
Details 詳細情報について
-
- CRID
- 1390001204871594368
-
- NII Article ID
- 130000079613
-
- ISSN
- 13497235
- 09182918
-
- Text Lang
- en
-
- Data Source
-
- JaLC
- Crossref
- CiNii Articles
- KAKEN
-
- Abstract License Flag
- Disallowed