Huntingtin inclusions do not down-regulate specific genes in the R6/2 Huntington's disease mouse

被引:21
作者
Sadri-Vakili, G.
Menon, A. S.
Farrell, L. A.
Keller-McGandy, C. E.
Cantuti-Castelvetri, I.
Standaert, D. G.
Augood, S. J.
Yohrling, G. J.
Cha, J-H. J.
机构
[1] Massachusetts Gen Hosp, MassGen Inst Neurodegenerat Dis, Charlestown, MA 02129 USA
[2] Johnson & Johnson Pharmaceut, Res & Dev LLC, Spring House, PA 19477 USA
关键词
Huntington's disease; in situ hybridization; inclusions; laser capture microdissection; striatum; transcription;
D O I
10.1111/j.1460-9568.2006.04871.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Transcriptional dysregulation is a central pathogenic mechanism in Huntington's disease (HD); HID and transgenic mouse models of HID demonstrate down-regulation of specific genes at the level of mRNA expression. Furthermore, neuronal intranuclear inclusions (NIIs) have been identified in the brains of R6/2 mice and HID patients. One possibility is that NIIs contribute to transcriptional dysregulation by sequestering transcription factors. We therefore assessed the relationship between NIIs and transcriptional dysregulation in the R6/2 mouse, using double-label in situ hybridization combined with immunohistochemistry, and laser capture microdissection combined with quantitative real-time PCR. There was no difference in transcript levels of specific genes between NII-positive and Nil-negative neurons. These results demonstrate that NIIs do not cause decreases in D2, PPE and PSS mRNA levels in R6/2 striatum and therefore are not involved in the down-regulation of these specific genes in this HID model. In addition, these observations argue against the notion that NIIs protect against transcriptional dysregulation in HID.
引用
收藏
页码:3171 / 3175
页数:5
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