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Death receptor 4 is preferentially recruited to lipid rafts in chronic lymphocytic leukemia cells contributing to tumor necrosis related apoptosis inducing ligand-induced synergistic apoptotic responses.死亡受体 4 优先募集到慢性淋巴细胞白血病细胞中的脂筏中,有助于肿瘤坏死相关凋亡诱导配体诱导的协同凋亡反应。
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Edelfosine and perifosine induce selective apoptosis in multiple myeloma by recruitment of death receptors and downstream signaling molecules into lipid rafts.依地福新和哌立福新通过将死亡受体和下游信号分子募集到脂筏中,诱导多发性骨髓瘤细胞发生选择性凋亡。
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本文引用的文献

1
Glucocorticoid-induced suppression of β-cell proliferation is mediated by Mig6.糖皮质激素诱导的β细胞增殖抑制是由 Mig6 介导的。
Endocrinology. 2013 Mar;154(3):1039-46. doi: 10.1210/en.2012-1923. Epub 2013 Feb 5.
2
Mig6 is a sensor of EGF receptor inactivation that directly activates c-Abl to induce apoptosis during epithelial homeostasis.Mig6 是 EGF 受体失活的传感器,它在上皮细胞稳态过程中直接激活 c-Abl 诱导细胞凋亡。
Dev Cell. 2012 Sep 11;23(3):547-59. doi: 10.1016/j.devcel.2012.08.001.
3
Ack1 tyrosine kinase activation correlates with pancreatic cancer progression.Ack1 酪氨酸激酶的激活与胰腺癌的进展相关。
Am J Pathol. 2012 Apr;180(4):1386-93. doi: 10.1016/j.ajpath.2011.12.028. Epub 2012 Feb 7.
4
Constitutive activated Cdc42-associated kinase (Ack) phosphorylation at arrested endocytic clathrin-coated pits of cells that lack dynamin.在缺乏动力蛋白的细胞中,组成性激活的 Cdc42 相关激酶(ACK)在被阻断的网格蛋白包被陷窝处发生磷酸化。
Mol Biol Cell. 2011 Feb 15;22(4):493-502. doi: 10.1091/mbc.E10-07-0637. Epub 2010 Dec 17.
5
Palmitoylation regulates raft affinity for the majority of integral raft proteins.棕榈酰化调节筏的大部分整体筏蛋白的亲和力。
Proc Natl Acad Sci U S A. 2010 Dec 21;107(51):22050-4. doi: 10.1073/pnas.1016184107. Epub 2010 Dec 3.
6
Proapoptotic DR4 and DR5 signaling in cancer cells: toward clinical translation.促进凋亡的 DR4 和 DR5 信号在癌细胞中的作用:迈向临床转化。
Curr Opin Cell Biol. 2010 Dec;22(6):837-44. doi: 10.1016/j.ceb.2010.08.001. Epub 2010 Aug 31.
7
Effect of Ack1 tyrosine kinase inhibitor on ligand-independent androgen receptor activity.Ack1 酪氨酸激酶抑制剂对配体非依赖性雄激素受体活性的影响。
Prostate. 2010 Sep 1;70(12):1274-85. doi: 10.1002/pros.21163.
8
New insights into apoptosis signaling by Apo2L/TRAIL.Apo2L/TRAIL 诱导细胞凋亡信号的新见解。
Oncogene. 2010 Aug 26;29(34):4752-65. doi: 10.1038/onc.2010.221. Epub 2010 Jun 7.
9
Somatic mutation in the ACK1 ubiquitin association domain enhances oncogenic signaling through EGFR regulation in renal cancer derived cells.在肾癌衍生细胞中,ACK1 泛素结合域中的体细胞突变通过调节 EGFR 增强致癌信号。
Mol Oncol. 2010 Aug;4(4):323-34. doi: 10.1016/j.molonc.2010.03.001. Epub 2010 Mar 19.
10
Cancer-associated mutations activate the nonreceptor tyrosine kinase Ack1.癌症相关突变激活非受体酪氨酸激酶 Ack1。
J Biol Chem. 2010 Apr 2;285(14):10605-15. doi: 10.1074/jbc.M109.060459. Epub 2010 Jan 28.

激活的 Cdc42 相关激酶 1(Ack1)对于肿瘤坏死因子相关凋亡诱导配体(TRAIL)受体向脂筏的募集和细胞死亡的诱导是必需的。

Activated Cdc42-associated kinase 1 (Ack1) is required for tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) receptor recruitment to lipid rafts and induction of cell death.

机构信息

From the Wolfson Institute for Biomedical Research, University College London, WC1E 6BT London, United Kingdom.

出版信息

J Biol Chem. 2013 Nov 15;288(46):32922-31. doi: 10.1074/jbc.M113.481507. Epub 2013 Oct 1.

DOI:10.1074/jbc.M113.481507
PMID:24085293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3829143/
Abstract

TNF-related apoptosis-inducing ligand (TRAIL) holds promise for treatment of cancer due to its ability to selectively kill cancer cells while sparing normal cells. Ligand-induced translocation of TRAIL receptors (TRAIL-R) 1 and 2 (also called DR4 and DR5, respectively) into lipid raft membrane microdomains is required for TRAIL-induced cell death by facilitating receptor clustering and formation of the death-inducing signaling complex, yet the underlying regulatory mechanisms remain largely unknown. We show here that the non-receptor tyrosine kinase Ack1, previously implicated in the spatiotemporal regulation of the EGF receptor, is required for TRAIL-induced cell death in multiple epithelial cell lines. TRAIL triggered a transient up-regulation of Ack1 and its recruitment to lipid rafts along with TRAIL-R1/2. siRNA-mediated depletion of Ack1 disrupted TRAIL-induced accumulation of TRAIL-R1/2 in lipid rafts and efficient recruitment of caspase-8 to the death-inducing signaling complex. Pharmacological inhibition of Ack1 did not affect TRAIL-induced cell death, indicating that Ack1 acts in a kinase-independent manner to promote TRAIL-R1/2 accumulation in lipid rafts. These findings identify Ack1 as an essential player in the spatial regulation of TRAIL-R1/2.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)因其能够选择性地杀死癌细胞而不伤害正常细胞,因此有望用于癌症治疗。配体诱导的 TRAIL 受体(TRAIL-R)1 和 2(分别称为 DR4 和 DR5)向脂筏膜微域的易位是 TRAIL 诱导细胞死亡所必需的,因为它促进了受体聚集和死亡信号转导复合物的形成,但潜在的调节机制在很大程度上仍然未知。我们在这里表明,先前涉及表皮生长因子受体时空调节的非受体酪氨酸激酶 Ack1,是多种上皮细胞系中 TRAIL 诱导细胞死亡所必需的。TRAIL 触发 Ack1 的短暂上调及其与 TRAIL-R1/2 一起向脂筏的募集。siRNA 介导的 Ack1 耗竭破坏了 TRAIL 在脂筏中诱导的 TRAIL-R1/2 积累和 caspase-8 向死亡信号转导复合物的有效募集。Ack1 的药理学抑制不影响 TRAIL 诱导的细胞死亡,表明 Ack1 以激酶非依赖性方式促进 TRAIL-R1/2 在脂筏中的积累。这些发现确定 Ack1 是 TRAIL-R1/2 空间调节中的一个重要参与者。