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本文引用的文献

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(Neuro)degenerated Mitochondria-ER contacts.(神经)退化的线粒体-内质网接触位点
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Cancer Stem Cell-Secreted Macrophage Migration Inhibitory Factor Stimulates Myeloid Derived Suppressor Cell Function and Facilitates Glioblastoma Immune Evasion.癌症干细胞分泌的巨噬细胞迁移抑制因子刺激髓源性抑制细胞功能并促进胶质母细胞瘤的免疫逃逸。
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Glioma Stemlike Cells Enhance the Killing of Glioma Differentiated Cells by Cytotoxic Lymphocytes.胶质瘤干细胞样细胞增强细胞毒性淋巴细胞对胶质瘤分化细胞的杀伤作用。
PLoS One. 2016 Apr 13;11(4):e0153433. doi: 10.1371/journal.pone.0153433. eCollection 2016.
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Integrated Transcriptomic and Glycomic Profiling of Glioma Stem Cell Xenografts.胶质瘤干细胞异种移植瘤的转录组和糖组综合分析
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Novel Cell-Penetrating Peptide-Based Vaccine Induces Robust CD4+ and CD8+ T Cell-Mediated Antitumor Immunity.新型穿膜肽基疫苗诱导强烈的 CD4+ 和 CD8+ T 细胞介导的抗肿瘤免疫。
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Mitochondrial control by DRP1 in brain tumor initiating cells.动力相关蛋白1(DRP1)对脑肿瘤起始细胞的线粒体调控
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Glycosylation and cancer: moving glycomics to the forefront.糖基化与癌症:将糖组学推向前沿
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F-actin flow drives affinity maturation and spatial organization of LFA-1 at the immunological synapse.F-肌动蛋白流驱动免疫突触处LFA-1的亲和力成熟和空间组织。
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9
Periostin secreted by glioblastoma stem cells recruits M2 tumour-associated macrophages and promotes malignant growth.胶质母细胞瘤干细胞分泌的骨膜蛋白招募M2型肿瘤相关巨噬细胞并促进恶性生长。
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10
Granzyme B-induced mitochondrial ROS are required for apoptosis.颗粒酶B诱导的线粒体活性氧是细胞凋亡所必需的。
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内质网-线粒体接触调控胶质瘤干细胞样细胞的表面聚糖表达及对杀伤性淋巴细胞的敏感性。

ER-mitochondria contacts control surface glycan expression and sensitivity to killer lymphocytes in glioma stem-like cells.

作者信息

Bassoy Esen Yonca, Kasahara Atsuko, Chiusolo Valentina, Jacquemin Guillaume, Boydell Emma, Zamorano Sebastian, Riccadonna Cristina, Pellegatta Serena, Hulo Nicolas, Dutoit Valérie, Derouazi Madiha, Dietrich Pierre Yves, Walker Paul R, Martinvalet Denis

机构信息

Department of Cell Physiology and Metabolism, University of Geneva, Geneva, Switzerland.

Laboratory of Molecular Neuropharmacology, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, Japan.

出版信息

EMBO J. 2017 Jun 1;36(11):1493-1512. doi: 10.15252/embj.201695429. Epub 2017 Mar 10.

DOI:10.15252/embj.201695429
PMID:28283580
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5452011/
Abstract

Glioblastoma is a highly heterogeneous aggressive primary brain tumor, with the glioma stem-like cells (GSC) being more sensitive to cytotoxic lymphocyte-mediated killing than glioma differentiated cells (GDC). However, the mechanism behind this higher sensitivity is unclear. Here, we found that the mitochondrial morphology of GSCs modulates the ER-mitochondria contacts that regulate the surface expression of sialylated glycans and their recognition by cytotoxic T lymphocytes and natural killer cells. GSCs displayed diminished ER-mitochondria contacts compared to GDCs. Forced ER-mitochondria contacts in GSCs increased their cell surface expression of sialylated glycans and reduced their susceptibility to cytotoxic lymphocytes. Therefore, mitochondrial morphology and dynamism dictate the ER-mitochondria contacts in order to regulate the surface expression of certain glycans and thus play a role in GSC recognition and elimination by immune effector cells. Targeting the mitochondrial morphology, dynamism, and contacts with the ER could be an innovative strategy to deplete the cancer stem cell compartment to successfully treat glioblastoma.

摘要

胶质母细胞瘤是一种高度异质性的侵袭性原发性脑肿瘤,其中胶质瘤干细胞(GSC)比胶质瘤分化细胞(GDC)对细胞毒性淋巴细胞介导的杀伤更敏感。然而,这种更高敏感性背后的机制尚不清楚。在这里,我们发现GSC的线粒体形态调节内质网-线粒体接触,这种接触调节唾液酸化聚糖的表面表达及其被细胞毒性T淋巴细胞和自然杀伤细胞的识别。与GDC相比,GSC显示出内质网-线粒体接触减少。在GSC中强制内质网-线粒体接触增加了它们唾液酸化聚糖的细胞表面表达,并降低了它们对细胞毒性淋巴细胞的敏感性。因此,线粒体形态和动态性决定了内质网-线粒体接触,以调节某些聚糖的表面表达,从而在免疫效应细胞识别和清除GSC中发挥作用。靶向线粒体形态、动态性以及与内质网的接触可能是一种创新策略,以耗尽癌症干细胞区室从而成功治疗胶质母细胞瘤。