Arboleda-Velasquez Joseph F, Zhou Zhipeng, Shin Hwa Kyoung, Louvi Angeliki, Kim Hyung-Hwan, Savitz Sean I, Liao James K, Salomone Salvatore, Ayata Cenk, Moskowitz Michael A, Artavanis-Tsakonas Spyros
Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2008 Mar 25;105(12):4856-61. doi: 10.1073/pnas.0709867105. Epub 2008 Mar 17.
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.
血管平滑肌细胞(SMCs)与中风的病理生理学有关,中风是全球第三大常见死因和长期神经功能障碍的主要原因。然而,对于将SMC功能与脑缺血易感性联系起来的潜在细胞途径,我们了解甚少。利用一种此前未被描述的Notch 3基因敲除小鼠模型(Notch 3是一种在血管平滑肌细胞中高度表达的Notch信号受体旁系同源物),我们发现该模型在受到刺激后对缺血性中风具有显著的易感性。对这些动物来源的血管平滑肌细胞进行细胞和分子分析,将Notch 3活性与特定基因靶点的表达联系起来,而基因拯救实验明确地将血管中的Notch 3功能与缺血表型联系起来。