| Literature DB >> 18347334 |
Joseph F Arboleda-Velasquez1, Zhipeng Zhou, Hwa Kyoung Shin, Angeliki Louvi, Hyung-Hwan Kim, Sean I Savitz, James K Liao, Salvatore Salomone, Cenk Ayata, Michael A Moskowitz, Spyros Artavanis-Tsakonas.
Abstract
Vascular smooth muscle cells (SMCs) have been implicated in the pathophysiology of stroke, the third most common cause of death and the leading cause of long-term neurological disability in the world. However, there is little insight into the underlying cellular pathways that link SMC function to brain ischemia susceptibility. Using a hitherto uncharacterized knockout mouse model of Notch 3, a Notch signaling receptor paralogue highly expressed in vascular SMCs, we uncover a striking susceptibility to ischemic stroke upon challenge. Cellular and molecular analyses of vascular SMCs derived from these animals associate Notch 3 activity to the expression of specific gene targets, whereas genetic rescue experiments unambiguously link Notch 3 function in vessels to the ischemic phenotype.Entities:
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Year: 2008 PMID: 18347334 PMCID: PMC2290794 DOI: 10.1073/pnas.0709867105
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205