Suppr超能文献

β-arrestin1 和独特的 CXCR4 结构对于基质衍生因子-1 下调神经母细胞瘤中 CXCR4 的细胞表面水平是必需的。

β-Arrestin1 and distinct CXCR4 structures are required for stromal derived factor-1 to downregulate CXCR4 cell-surface levels in neuroblastoma.

机构信息

Neurobiology of Disease (I.C.C.), Molecular Pharmacology and Experimental Therapeutics (A.O.B.), and Department of Immunology (C.R.-R., K.N.K., K.E.H.), Mayo Clinic College of Medicine, Mayo Graduate School, Mayo Clinic, Rochester, Minnesota.

出版信息

Mol Pharmacol. 2014 Apr;85(4):542-52. doi: 10.1124/mol.113.089714. Epub 2014 Jan 22.

Abstract

CXC chemokine receptor 4 (CXCR4) is a G protein-coupled receptor (GPCR) located on the cell surface that signals upon binding the chemokine stromal derived factor-1 (SDF-1; also called CXCL 12). CXCR4 promotes neuroblastoma proliferation and chemotaxis. CXCR4 expression negatively correlates with prognosis and drives neuroblastoma growth and metastasis in mouse models. All functions of CXCR4 require its expression on the cell surface, yet the molecular mechanisms that regulate CXCR4 cell-surface levels in neuroblastoma are poorly understood. We characterized CXCR4 cell-surface regulation in the related SH-SY5Y and SK-N-SH human neuroblastoma cell lines. SDF-1 treatment caused rapid down-modulation of CXCR4 in SH-SY5Y cells. Pharmacologic activation of protein kinase C similarly reduced CXCR4, but via a distinct mechanism. Analysis of CXCR4 mutants delineated two CXCR4 regions required for SDF-1 treatment to decrease cell-surface CXCR4 in neuroblastoma cells: the isoleucine-leucine motif at residues 328 and 329 and residues 343-352. In contrast, and unlike CXCR4 regulation in other cell types, serines 324, 325, 338, and 339 were not required. Arrestin proteins can bind and regulate GPCR cell-surface expression, often functioning together with kinases such as G protein-coupled receptor kinase 2 (GRK2). Using SK-N-SH cells which are naturally deficient in β-arrestin1, we showed that β-arrestin1 is required for the CXCR4 343-352 region to modulate CXCR4 cell-surface expression following treatment with SDF-1. Moreover, GRK2 overexpression enhanced CXCR4 internalization, via a mechanism requiring both β-arrestin1 expression and the 343-352 region. Together, these results characterize CXCR4 structural domains and β-arrestin1 as critical regulators of CXCR4 cell-surface expression in neuroblastoma. β-Arrestin1 levels may therefore influence the CXCR4-driven metastasis of neuroblastoma as well as prognosis.

摘要

CXC 趋化因子受体 4(CXCR4)是一种位于细胞表面的 G 蛋白偶联受体(GPCR),与趋化因子基质衍生因子-1(SDF-1;也称为 CXCL12)结合后会发出信号。CXCR4 促进神经母细胞瘤的增殖和趋化作用。CXCR4 的表达与预后呈负相关,并在小鼠模型中驱动神经母细胞瘤的生长和转移。CXCR4 的所有功能都需要其在细胞表面表达,然而,调节神经母细胞瘤中 CXCR4 细胞表面水平的分子机制还知之甚少。我们在相关的 SH-SY5Y 和 SK-N-SH 人神经母细胞瘤细胞系中对 CXCR4 的细胞表面调节进行了表征。SDF-1 处理导致 SH-SY5Y 细胞中 CXCR4 的快速下调。蛋白激酶 C 的药理学激活也降低了 CXCR4,但通过一种不同的机制。对 CXCR4 突变体的分析描绘了两个 CXCR4 区域,这些区域对于 SDF-1 处理来减少神经母细胞瘤细胞表面的 CXCR4 是必需的:残基 328 和 329 处的异亮氨酸-亮氨酸基序和残基 343-352。相比之下,与其他细胞类型中 CXCR4 的调节不同,丝氨酸 324、325、338 和 339 不是必需的。 arrestin 蛋白可以结合并调节 GPCR 细胞表面表达,通常与 G 蛋白偶联受体激酶 2(GRK2)等激酶一起发挥作用。使用天然缺乏β-arrestin1 的 SK-N-SH 细胞,我们表明β-arrestin1 是调节 SDF-1 处理后 CXCR4 细胞表面表达所必需的,这是通过 343-352 区域实现的。此外,GRK2 的过表达通过一种需要β-arrestin1 表达和 343-352 区域的机制增强了 CXCR4 的内化。总之,这些结果将 CXCR4 结构域和β-arrestin1 描绘为神经母细胞瘤中 CXCR4 细胞表面表达的关键调节剂。β-arrestin1 的水平因此可能会影响神经母细胞瘤的 CXCR4 驱动转移以及预后。

相似文献

3
Role of tyrosine phosphorylation in ligand-independent sequestration of CXCR4 in human primary monocytes-macrophages.
J Biol Chem. 2001 Dec 28;276(52):49236-43. doi: 10.1074/jbc.M108523200. Epub 2001 Oct 19.
5
Atypical Chemokine Receptor 3 "Senses" CXC Chemokine Receptor 4 Activation Through GPCR Kinase Phosphorylation.
Mol Pharmacol. 2023 Oct;104(4):174-186. doi: 10.1124/molpharm.123.000710. Epub 2023 Jul 20.
9
Post-endocytic fates of delta-opioid receptor are regulated by GRK2-mediated receptor phosphorylation and distinct beta-arrestin isoforms.
J Neurochem. 2008 Jul;106(2):781-92. doi: 10.1111/j.1471-4159.2008.05431.x. Epub 2008 Apr 17.
10
X4 HIV-1 induces neuroblastoma cell death by interference with CXCL12/CXCR4 interaction.
Cell Mol Biol (Noisy-le-grand). 2003;49 Online Pub:OL443-52.

引用本文的文献

1
Screening for gene expression fluctuations reveals latency-promoting agents of HIV.
Proc Natl Acad Sci U S A. 2021 Mar 16;118(11). doi: 10.1073/pnas.2012191118.
2
Cell size dependent migration of T-cells latently infected with HIV.
J Life Sci (Westlake Village). 2020 Mar;2(1):1-10. doi: 10.36069/JoLS/20200301.
7
A single amino acid substitution in CXCL12 confers functional selectivity at the beta-arrestin level.
Oncotarget. 2018 Jun 22;9(48):28830-28841. doi: 10.18632/oncotarget.25533.
8
β-Arrestin2 mediates progression of murine primary myelofibrosis.
JCI Insight. 2017 Dec 21;2(24):98094. doi: 10.1172/jci.insight.98094.
9
Effects of SDF-1/CXCR4 on the Repair of Traumatic Brain Injury in Rats by Mediating Bone Marrow Derived Mesenchymal Stem Cells.
Cell Mol Neurobiol. 2018 Mar;38(2):467-477. doi: 10.1007/s10571-017-0490-4. Epub 2017 May 8.

本文引用的文献

2
Comprehensive cytogenomic profile of the in vitro neuronal model SH-SY5Y.
Neurogenetics. 2013 Feb;14(1):63-70. doi: 10.1007/s10048-012-0350-9. Epub 2012 Dec 9.
3
Establishment and characterization of xenograft models of human neuroblastoma bone metastasis.
Childs Nerv Syst. 2012 Dec;28(12):2047-54. doi: 10.1007/s00381-012-1909-3. Epub 2012 Sep 16.
4
Involvement of the CXCR7/CXCR4/CXCL12 axis in the malignant progression of human neuroblastoma.
PLoS One. 2012;7(8):e43665. doi: 10.1371/journal.pone.0043665. Epub 2012 Aug 20.
6
A review on CXCR4/CXCL12 axis in oncology: no place to hide.
Eur J Cancer. 2013 Jan;49(1):219-30. doi: 10.1016/j.ejca.2012.05.005. Epub 2012 Jun 9.
7
The chemokine superfamily revisited.
Immunity. 2012 May 25;36(5):705-16. doi: 10.1016/j.immuni.2012.05.008.
8
Neuroblastoma.
Semin Pediatr Surg. 2012 Feb;21(1):2-14. doi: 10.1053/j.sempedsurg.2011.10.009.
9
C-terminal di-leucine motif of dopamine D₁ receptor plays an important role in its plasma membrane trafficking.
PLoS One. 2011;6(12):e29204. doi: 10.1371/journal.pone.0029204. Epub 2011 Dec 19.
10
Neuroblastoma therapy: what is in the pipeline?
Endocr Relat Cancer. 2011 Nov 14;18(6):R213-31. doi: 10.1530/ERC-11-0251. Print 2011 Dec.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验