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Direct Protein Delivery to Mammalian Cells Using Cell-permeable Cys2-His2 Zinc-finger Domains
Published on: March 25, 2015
Increased expression of Myc-interacting zinc finger protein 1 in APP/PS1 mice
Lu Liu1, Yu-Jie Lai2, Li-Ge Zhao1
1Department of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing Key Laboratory of Neurology, Chongqing 400016, P.R. China.
Abstract:
Myc-interacting zinc-finger protein 1 (Miz1) is a member of the poxvirus and zinc-finger domain/zinc finger transcription factor family. Its transcription activation and repression functions in the nucleus are well elucidated; however its cytoplasmic inflammation function is poorly understood and may be associated with the pathogenesis of Alzheimer's disease (AD). The aim of the present study was to investigate the association between AD and Miz1 expression. In the present study, the expression and distribution of Miz1 in wild-type (WT) and amyloid precursor protein/presenelin-1 (AD) mice was studied using reverse transcription-quantitative polymerase chain reaction, western blot analysis, and immunohistochemical and immunofluorescence staining. The results indicated that Miz1 was significantly upregulated in the cortex of AD mice (P<0.05). Double immunofluorescence labeling revealed that Miz1 protein was predominantly expressed in neurons and astrocytes, as evidenced by co-localization with the dendritic markers microtubule associated protein 2 and glial fibrillary acidic protein, respectively. The results of the present study suggest that the expression of Miz1 in the brain tissue of AD mice may serve an important role in AD pathogenesis.
Insights
Myc-interacting zinc-finger protein 1 (Miz1) expression is elevated in Alzheimer's disease (AD) mouse models. This protein is found in neurons and astrocytes, suggesting a role for Miz1 in AD pathogenesis.
Area of Science:
- Neuroscience
- Molecular Biology
- Pathology
Background:
- Myc-interacting zinc-finger protein 1 (Miz1) is a transcription factor with known nuclear functions.
- Miz1's role in cytoplasmic inflammation and its association with Alzheimer's disease (AD) pathogenesis are poorly understood.
Purpose of the Study:
- To investigate the association between Alzheimer's disease and Miz1 expression in the brain.
- To determine the cellular localization of Miz1 in AD mouse models.
Main Methods:
- Utilized reverse transcription-quantitative polymerase chain reaction (RT-qPCR) and western blot analysis to assess Miz1 expression levels.
- Employed immunohistochemical and immunofluorescence staining to examine Miz1 distribution in wild-type and AD mouse brains.
- Performed double immunofluorescence labeling to identify Miz1-expressing cell types, co-localizing with neuronal (MAP2) and astrocytic (GFAP) markers.
Main Results:
- Miz1 expression was significantly upregulated in the cortex of AD mice compared to wild-type controls (P<0.05).
- Miz1 protein was predominantly detected in neurons and astrocytes within the brain tissue.
- Co-localization studies confirmed Miz1 presence in both neuronal and glial cells.
Conclusions:
- Miz1 expression is elevated in the brains of AD mice.
- Miz1 is localized in key brain cells, including neurons and astrocytes, relevant to AD pathology.
- These findings suggest Miz1 plays a significant role in the pathogenesis of Alzheimer's disease.
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