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低密度脂蛋白受体相关蛋白 1 介导 Notch 通路的激活。

Low-density-lipoprotein-receptor-related protein 1 mediates Notch pathway activation.

机构信息

Key Laboratory of Structural Biology of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou 310024, Zhejiang, China; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou 310024, Zhejiang, China; Institute of Biology, Westlake Institute for Advanced Study, Hangzhou 310024, Zhejiang, China.

Department of Experimental Radiation Oncology, the University of Texas M D Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Dev Cell. 2021 Oct 25;56(20):2902-2919.e8. doi: 10.1016/j.devcel.2021.09.015. Epub 2021 Oct 8.

Abstract

The Notch signaling pathway controls cell growth, differentiation, and fate decisions, and its dysregulation has been linked to various human genetic disorders and cancers. To comprehensively understand the global organization of the Notch pathway and identify potential drug targets for Notch-related diseases, we established a protein interaction landscape for the human Notch pathway. By combining and analyzing genetic and phenotypic data with bioinformatics analysis, we greatly expanded this pathway and identified many key regulators, including low-density-lipoprotein-receptor-related protein 1 (LRP1). We demonstrated that LRP1 mediates the ubiquitination chain linkage switching of Delta ligands, which further affects ligand recycling, membrane localization, and stability. LRP1 inhibition led to Notch signaling inhibition and decreased tumorigenesis in leukemia models. Our study provides a glimpse into the Notch pathway interaction network and uncovers LRP1 as one critical regulator of the Notch pathway, as well as a possible therapeutic target for Notch-related cancers.

摘要

Notch 信号通路控制着细胞的生长、分化和命运决定,其失调与各种人类遗传疾病和癌症有关。为了全面了解 Notch 通路的全局组织,并确定 Notch 相关疾病的潜在药物靶点,我们建立了人类 Notch 通路的蛋白质相互作用图谱。通过结合和分析遗传和表型数据与生物信息学分析,我们大大扩展了这个通路,并鉴定了许多关键的调节剂,包括低密度脂蛋白受体相关蛋白 1(LRP1)。我们证明了 LRP1 介导 Delta 配体的泛素化链连接转换,这进一步影响了配体的回收、膜定位和稳定性。LRP1 抑制导致 Notch 信号抑制,并减少白血病模型中的肿瘤发生。我们的研究提供了 Notch 通路相互作用网络的一个视角,并揭示了 LRP1 作为 Notch 通路的一个关键调节剂,以及 Notch 相关癌症的一个可能的治疗靶点。

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