کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
9425510 | 1295877 | 2005 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Neuronal intranuclear inclusions and neuropil aggregates in HdhCAG(150) knockin mice
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کلمات کلیدی
CBPTris-buffered saline with 0.05% Tween-20httTBSTPolyQDABDARPP-32SCAAtaxia - آتاکسی spinocerebellar ataxia - آتاکسی spinocerebellarStriatum - استریاتومphosphate buffer - بافر فسفاتHuntington disease - بیماری هانتینگتونNeurodegeneration - تولید نوروژنیکNeuronal intranuclear inclusions - درگیری های میان هسته ای عصبیRoom temperature - دمای اتاقdiaminobenzidine - دیامینو بنزیدینKnockin - ناکینhuntingtin protein - پروتئین huntingtincyclic AMP response element binding protein - پروتئین اتصال دهنده عنصر پاسخ Cyclic AMPPolyglutamine - پلیگلوتامین
موضوعات مرتبط
علوم زیستی و بیوفناوری
علم عصب شناسی
علوم اعصاب (عمومی)
پیش نمایش صفحه اول مقاله
چکیده انگلیسی
We studied the development of neuronal intranuclear inclusions (NIIs), neuropil aggregates (NAs), and expression of expanded repeat polyglutamine protein in the HdhCAG(150) knockin mouse model of Huntington's disease (HD). Diffuse nuclear localization of huntingtin protein (htt) was noted initially within striatal neurons at approximately 28 weeks, followed by the development of striatal htt immunoreactive NIIs by approximately 40 weeks. Striatal NIIs were observed initially in clusters within the matrix compartment but subsequently became diffusely distributed throughout the striatum. In the oldest animals (107 weeks), NIIs were enlarged and diffuse nuclear htt immunoreactivity reduced. Expression of ubiquitin immunoreactive NIIs paralleled but lagged behind the expression of htt immunoreactive NIIs. Abundant NIIs were found by approximately 75 weeks in layers 3 and 4 of somatosensory cortex and in layer 2 of piriform cortex. In the oldest animals, greater than 100 weeks, some NIIs were found in many brain regions. NAs were found mainly within the globus pallidus and substantia nigra, perhaps reflecting expression in striatal terminals. Cyclic AMP response element binding protein (CBP) was not localized to NIIs, arguing against gross sequestration of this transcriptionally active protein. Comparison of the relative levels of a common polyglutamine epitope in HdhCAG(150) knockin and hprtCAG(146) knockin mice shows greater expression of the polyglutamine epitope in the phenotypically less aggressive HdhCAG(150) knockin line. HdhCAG(150) knockin mice may be a model of early pathologic changes in HD.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuroscience - Volume 131, Issue 4, 2005, Pages 843-852
Journal: Neuroscience - Volume 131, Issue 4, 2005, Pages 843-852
نویسندگان
S.J. Tallaksen-Greene, A.B. Crouse, J.M. Hunter, P.J. Detloff, R.L. Albin,