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将Notch信号通路与缺血性中风联系起来。

Linking Notch signaling to ischemic stroke.

作者信息

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

机构信息

Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 2008 Mar 25;105(12):4856-61. doi: 10.1073/pnas.0709867105. Epub 2008 Mar 17.

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.

摘要

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。

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Linking Notch signaling to ischemic stroke.将Notch信号通路与缺血性中风联系起来。
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