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Functional Implications of Plasma Membrane Condensation for T Cell Activation

机译:血浆膜浓缩对T细胞活化的功能意义

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摘要

The T lymphocyte plasma membrane condenses at the site of activation but the functional significance of this receptor-mediated membrane reorganization is not yet known. Here we demonstrate that membrane condensation at the T cell activation sites can be inhibited by incorporation of the oxysterol 7-ketocholesterol (7KC), which is known to prevent the formation of raft-like liquid-ordered domains in model membranes. We enriched T cells with 7KC, or cholesterol as control, to assess the importance of membrane condensation for T cell activation. Upon 7KC treatment, T cell antigen receptor (TCR) triggered calcium fluxes and early tyrosine phosphorylation events appear unaltered. However, signaling complexes form less efficiently on the cell surface, fewer phosphorylated signaling proteins are retained in the plasma membrane and actin restructuring at activation sites is impaired in 7KC-enriched cells resulting in compromised downstream activation responses. Our data emphasizes lipids as an important medium for the organization at T cell activation sites and strongly indicates that membrane condensation is an important element of the T cell activation process.
机译:T淋巴细胞质膜在激活位点凝结,但这种受体介导的膜重组的功能意义尚不清楚。在这里,我们证明可以通过并入氧固醇7-酮胆固醇(7KC)来抑制T细胞活化位点处的膜凝结,这已知可以防止模型膜中筏状液体有序域的形成。我们用7KC或胆固醇作为对照富集了T细胞,以评估膜凝结对T细胞活化的重要性。经过7KC处理后,T细胞抗原受体(TCR)触发了钙通量,早期酪氨酸磷酸化事件似乎没有改变。然而,信号复合物在细胞表面上形成的效率较低,较少的磷酸化信号蛋白保留在质膜中,并且在富含7KC的细胞中,肌动蛋白在激活位点的重构受到损害,导致下游激活反应受损。我们的数据强调脂质是组织在T细胞活化位点的重要介质,并强烈表明膜凝结是T细胞活化过程的重要元素。

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