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脂质驱动的质膜层间耦合调节肥大细胞中 FcεRI 信号转导。

Lipid-driven interleaflet coupling of plasma membrane order regulates FcεRI signaling in mast cells.

机构信息

Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York.

Department of Biochemistry and Cell Biology, Stony Brook University, Stony Brook, New York.

出版信息

Biophys J. 2024 Aug 6;123(15):2256-2270. doi: 10.1016/j.bpj.2023.07.027. Epub 2023 Aug 1.

Abstract

Interleaflet coupling-the influence of one leaflet on the properties of the opposing leaflet-is a fundamental plasma membrane organizational principle. This coupling is proposed to participate in maintaining steady-state biophysical properties of the plasma membrane, which in turn regulates some transmembrane signaling processes. A prominent example is antigen (Ag) stimulation of signaling by clustering transmembrane receptors for immunoglobulin E (IgE), FcεRI. This transmembrane signaling depends on the stabilization of ordered regions in the inner leaflet for sorting of intracellular signaling components. The resting inner leaflet has a lipid composition that is generally less ordered than the outer leaflet and that does not spontaneously phase separate in model membranes. We propose that interleaflet coupling can mediate ordering and disordering of the inner leaflet, which is poised in resting cells to reorganize upon stimulation. To test this in live cells, we first established a straightforward approach to evaluate induced changes in membrane order by measuring inner leaflet diffusion of lipid probes by imaging fluorescence correlation spectroscopy, by imaging fluorescence correlation spectroscopy (ImFCS), before and after methyl-α-cyclodexrin (mαCD)-catalyzed exchange of outer leaflet lipids (LEX) with exogenous order- or disorder-promoting phospholipids. We examined the functional impact of LEX by monitoring two Ag-stimulated responses: recruitment of cytoplasmic Syk kinase to the inner leaflet and exocytosis of secretory granules (degranulation). Based on the ImFCS data in resting cells, we observed global increase or decrease of inner leaflet order when outer leaflet is exchanged with order- or disorder-promoting lipids, respectively. We find that the degree of both stimulated Syk recruitment and degranulation correlates positively with LEX-mediated changes of inner leaflet order in resting cells. Overall, our results show that resting-state lipid ordering of the outer leaflet influences the ordering of the inner leaflet, likely via interleaflet coupling. This imposed lipid reorganization modulates transmembrane signaling stimulated by Ag clustering of IgE-FcεRI.

摘要

叶间耦合——一个叶层对相对叶层性质的影响——是一种基本的质膜组织原则。这种耦合被认为参与维持质膜的稳态生物物理性质,进而调节一些跨膜信号转导过程。一个突出的例子是抗原 (Ag) 通过聚集免疫球蛋白 E (IgE)、FcεRI 的跨膜受体来刺激信号转导。这种跨膜信号转导依赖于内层有序区域的稳定,以分选细胞内信号成分。静止的内层具有的脂质组成通常比外层无序,并且在模型膜中不会自发相分离。我们提出,叶间耦合可以介导内层的有序和无序,这在静止细胞中处于准备状态,在受到刺激时可以重新组织。为了在活细胞中验证这一点,我们首先建立了一种简单的方法,通过荧光相关光谱成像(ImFCS)测量脂质探针在内层的扩散,来评估膜有序性的诱导变化,然后用甲基-α-环糊精(mαCD)催化外叶层脂质(LEX)与外源性促进有序或无序的磷脂交换前后。我们通过监测两种 Ag 刺激的反应:细胞质 Syk 激酶向内层的募集和分泌颗粒(脱粒)的胞吐作用,来检查 LEX 的功能影响。基于静止细胞中的 ImFCS 数据,我们观察到当外层与促进有序或无序的脂质交换时,内层的全局有序性增加或减少。我们发现,两种受刺激的 Syk 募集和脱粒的程度都与 LEX 介导的静止细胞内层有序性变化呈正相关。总的来说,我们的结果表明,外层的静止状态脂质有序性影响内层的有序性,可能通过叶间耦合。这种强制的脂质重排调节了由 IgE-FcεRI 聚集刺激的跨膜信号转导。

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