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本文引用的文献

1
Cannabinoid Receptors and the Endocannabinoid System: Signaling and Function in the Central Nervous System.大麻素受体和内源性大麻素系统:中枢神经系统中的信号传递和功能。
Int J Mol Sci. 2018 Mar 13;19(3):833. doi: 10.3390/ijms19030833.
2
Fatty-acid-binding protein 5 controls retrograde endocannabinoid signaling at central glutamate synapses.脂肪酸结合蛋白 5 控制中枢谷氨酸突触的逆行内源性大麻素信号传递。
Proc Natl Acad Sci U S A. 2018 Mar 27;115(13):3482-3487. doi: 10.1073/pnas.1721339115. Epub 2018 Mar 12.
3
Cytokines Stimulate the Release of Microvesicles from Myeloid Cells Independently from the P2X7 Receptor/Acid Sphingomyelinase Pathway.细胞因子独立于 P2X7 受体/酸性鞘磷脂酶途径刺激髓样细胞释放微囊泡。
Front Immunol. 2018 Feb 7;9:204. doi: 10.3389/fimmu.2018.00204. eCollection 2018.
4
Functional Relevance of Endocannabinoid-Dependent Synaptic Plasticity in the Central Nervous System.内源性大麻素依赖的中枢神经系统突触可塑性的功能相关性。
ACS Chem Neurosci. 2018 Sep 19;9(9):2146-2161. doi: 10.1021/acschemneuro.7b00508. Epub 2018 Feb 19.
5
Sphingolipids role in the regulation of inflammatory response: From leukocyte biology to bacterial infection.鞘脂在炎症反应调控中的作用:从白细胞生物学到细菌感染。
J Leukoc Biol. 2018 Mar;103(3):445-456. doi: 10.1002/JLB.3MR0717-269R. Epub 2018 Jan 9.
6
ATP Modifies the Proteome of Extracellular Vesicles Released by Microglia and Influences Their Action on Astrocytes.三磷酸腺苷修饰小胶质细胞释放的细胞外囊泡蛋白质组并影响其对星形胶质细胞的作用。
Front Pharmacol. 2017 Dec 13;8:910. doi: 10.3389/fphar.2017.00910. eCollection 2017.
7
Neutral sphingomyelinases control extracellular vesicles budding from the plasma membrane.中性鞘磷脂酶控制从质膜出芽的细胞外囊泡。
J Extracell Vesicles. 2017 Sep 26;6(1):1378056. doi: 10.1080/20013078.2017.1378056. eCollection 2017.
8
Sphingolipid metabolism in cancer signalling and therapy.鞘脂代谢在癌症信号传导与治疗中的作用
Nat Rev Cancer. 2018 Jan;18(1):33-50. doi: 10.1038/nrc.2017.96. Epub 2017 Nov 17.
9
Extracellular vesicles in neurodegenerative diseases.细胞外囊泡在神经退行性疾病中的作用。
Mol Aspects Med. 2018 Apr;60:52-61. doi: 10.1016/j.mam.2017.11.006. Epub 2017 Nov 22.
10
Involvement of Gβγ subunits of G protein coupled with S1P receptor on multivesicular endosomes in F-actin formation and cargo sorting into exosomes.G 蛋白偶联的 S1P 受体与多泡体网格蛋白包被小泡中 Gβγ 亚基共同参与 F-actin 的形成和货物分选到外泌体中。
J Biol Chem. 2018 Jan 5;293(1):245-253. doi: 10.1074/jbc.M117.808733. Epub 2017 Nov 13.

鞘脂在细胞外囊泡的生物发生和生物学活性中的作用。

Role of sphingolipids in the biogenesis and biological activity of extracellular vesicles.

机构信息

Consiglio Nazionale delle Ricerche (CNR) Institute of Neuroscience, 20129 Milano, Italy

Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) Humanitas, 20089 Rozzano, Italy.

出版信息

J Lipid Res. 2018 Aug;59(8):1325-1340. doi: 10.1194/jlr.R083915. Epub 2018 May 31.

DOI:10.1194/jlr.R083915
PMID:29853528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6071771/
Abstract

Extracellular vesicles (EVs) are membrane vesicles released by both eukaryotic and prokaryotic cells; they not only serve physiological functions, such as disposal of cellular components, but also play pathophysiologic roles in inflammatory and degenerative diseases. Common molecular mechanisms for EV biogenesis are evident in different cell biological contexts across eukaryotic phyla, and inhibition of this biogenesis may provide an avenue for therapeutic research. The involvement of sphingolipids (SLs) and their enzymes on EV biogenesis and release has not received much attention in current research. Here, we review how SLs participate in EV biogenesis by shaping membrane curvature and how they contribute to EV action in target cells. First, we describe how acid and neutral SMases, by generating the constitutive SL, ceramide, facilitate biogenesis of EVs at the plasma membrane and inside the endocytic compartment. We then discuss the involvement of other SLs, such as sphingosine-1-phosphate and galactosyl-sphingosine, in EV formation and cargo sorting. Last, we look ahead at some biological effects of EVs mediated by changes in SL levels in recipient cells.

摘要

细胞外囊泡 (EVs) 是真核细胞和原核细胞释放的膜囊泡;它们不仅具有生理功能,如细胞成分的处理,而且在炎症和退行性疾病中发挥病理生理作用。在真核生物门的不同细胞生物学背景下,EV 生物发生的常见分子机制是明显的,而抑制这种生物发生可能为治疗研究提供途径。鞘脂类 (SLs) 及其在 EV 生物发生和释放中的酶的参与在当前研究中并没有受到太多关注。在这里,我们回顾了 SLs 如何通过塑造膜曲率来参与 EV 的生物发生,以及它们如何促进 EV 在靶细胞中的作用。首先,我们描述了酸性和中性 SMase 如何通过产生组成性 SL 神经酰胺,促进质膜和内吞体隔间中 EV 的生物发生。然后,我们讨论了其他 SL,如鞘氨醇-1-磷酸和半乳糖基鞘氨醇,在 EV 形成和货物分拣中的作用。最后,我们展望了 EV 通过改变受体细胞中 SL 水平介导的一些生物学效应。