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| Content Provider | PubMed Central |
|---|---|
| Author | Ran, Qi-shan Yu, Yun-hu Fu, Xiao-hong Wen, Yuan-chao |
| Copyright Year | 2015 |
| Abstract | The Notch signaling pathway plays a key role in angiogenesis and endothelial cell formation, but it remains unclear whether it is involved in vascular repair by endothelial progenitor cells after traumatic brain injury. Therefore, in the present study, we controlled the Notch signaling pathway using overexpression and knockdown constructs. Activation of the Notch signaling pathway by Notch1 or Jagged1 overexpression enhanced the migration, invasiveness and angiogenic ability of endothelial progenitor cells. Suppression of the Notch signaling pathway with Notch1 or Jagged1 siRNAs reduced the migratory capacity, invasiveness and angiogenic ability of endothelial progenitor cells. Activation of the Notch signaling pathway in vivo in a rat model of mild traumatic brain injury promoted neurovascular repair. These findings suggest that the activation of the Notch signaling pathway promotes blood vessel formation and tissue repair after brain trauma. |
| Related Links | http://dx.doi.org/10.4103/1673-5374.162758 |
| Ending Page | 1264 |
| Page Count | 7 |
| Starting Page | 1258 |
| File Format | |
| ISSN | 18767958 |
| e-ISSN | 18767958 |
| Journal | Neural Regeneration Research |
| Issue Number | 8 |
| Volume Number | 10 |
| Language | English |
| Publisher | Medknow Publications & Media Pvt Ltd |
| Publisher Date | 2015-08-01 |
| Access Restriction | Open |
| Rights Holder | Medknow Publications & Media Pvt Ltd |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Developmental Neuroscience |
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