کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
6280025 | 1615087 | 2016 | 5 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Research paperHypoxia-inducible factor-1a contributes to dendritic overgrowth in tuberous sclerosis Research paperHypoxia-inducible factor-1a contributes to dendritic overgrowth in tuberous sclerosis](/preview/png/6280025.png)
- Newborn Tsc1null neurons display increased dendritic arborization in addition to increased HIF1a levels.
- Decreasing HIF1a levels in Tsc1null neurons normalizes dendritic arborization.
- Increasing HIF1a levels in wild type neurons increases dendritic complexity and length.
Expression of hypoxia-inducible factor 1a (HIF1a) is increased under several pathological conditions such as hyperactive mechanistic target of rapamycin complex 1 (mTORC1) in tuberous sclerosis complex (TSC). Hyperactive mTORC1 and the resulting increased dendritic complexity of neurons are shared molecular and cellular alterations in several neurological disorders associated with cognitive disabilities. Despite some evidence that HIF1a contributes to dendritic overgrowth in vitro, it remains unknown whether increased HIF1a in TSC neurons could contribute to their increased dendritic complexity. To address this use in vivo, we generated TSC neurons by deleting Tsc1 in newborn olfactory bulb (OB) neurons of conditional Tsc1 transgenic mice using neonatal electroporation. In addition to their increased dendritic complexity, Tsc1null neurons have been reported to display increased Hif1a mRNA level and HIF1a transcriptional activity. We found that Tsc1null-dependent dendritic overgrowth was prevented by knocking down HIF1a or expressing a dominant negative HIF1a. In addition, overexpressing HIF1a in wild-type developing neurons resulted in increased dendritic complexity in vivo. These data highlight that an increase in HIF1a levels contributes to abnormal dendritic patterning in developing neurons under normal conditions and hyperactive mTORC1 conditions as in TSC.
Journal: Neuroscience Letters - Volume 612, 26 January 2016, Pages 43-47