کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
6273695 1614799 2014 18 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Immunolocalization of human alpha-synuclein in the Thy1-aSyn (“Line 61”) transgenic mouse line
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
Immunolocalization of human alpha-synuclein in the Thy1-aSyn (“Line 61”) transgenic mouse line
چکیده انگلیسی


- We have analyzed through a systematic approach the localization of human a-syn within the brain of adult Thy-1 a-syn mouse.
- We provide an anatomical map of the human a-syn distribution in the mouse line 61.
- The protein is present in many brain areas including some, but not all, prone to the formation of a-syn inclusions in PD.
- These data will help to relate a-syn expression to the phenotypic manifestations observed in this mouse line.

Alpha-synuclein (a-syn) is the major component of the intracytoplasmic inclusions known as Lewy bodies (LB), which constitute the hallmark of Parkinson's disease (PD). Mice overexpressing human a-syn under the Thy-1 promoter (ASO) show slow neurodegeneration and some behavioral deficits similar to those seen in human PD patients. Here, we describe a whole-brain distribution of human a-syn in adult ASO mice. We find that the human a-syn is ubiquitously distributed in the brain including the cerebellar cortex, but the intensity and sub-cellular localization of the staining differed in the various regions of the central nervous system. Among particular CNS areas with human a-syn immunoreactivity, we describe staining patterns in the olfactory bulb, cortex, hippocampus, thalamic region, brainstem nuclei and cerebellar cortex. This immunohistochemical study provides an anatomical map of the human a-syn distribution in ASO mice. Our data show that human a-syn, although not present at levels that were detectable by immunostaining in dopaminergic neurons of substantia nigra or noradrenergic neurons of locus coeruleus, was highly expressed in other PD relevant regions of the brain in different neuronal subtypes. These data will help to relate a-syn expression to the phenotypic manifestations observed in this widely used mouse line.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 277, 26 September 2014, Pages 647-664
نویسندگان
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