Harder T, Simons K
Max Planck Institute for Molecular Cell Biology and Genetics, and Cell Biology and Biophysics Programme, Heidelberg, Germany.
Eur J Immunol. 1999 Feb;29(2):556-62. doi: 10.1002/(SICI)1521-4141(199902)29:02<556::AID-IMMU556>3.0.CO;2-2.
Lateral cross-linking of glycosylphosphatidylinositol (GPI)-anchored proteins and glycosphingolipids can trigger a signaling cascade which leads to activation of lymphoid cells. A possible explanation how the signal is transduced through the plasma membrane has arisen from the concept of raft sphingolipid-cholesterol microdomains in cell membranes. Cross-linking of GPI-anchored proteins, glycolipids and other raft components leads to the formation of stabilized membrane patches in the plasma membrane which enrich members of the Src-tyrosine kinase family. We have studied cellular responses to raft patch formation in the Jurkat T cell line and in particular changes in the actin cytoskeleton. We found that raft patches formed by GPI-anchored CD59 protein and the ganglioside GM1 accumulate filamentous actin. Most interestingly, we observed a strong accumulation of tyrosine-phosphorylated proteins in raft patches, strongly supporting the view that they can function as centers of signal transduction. Using a Lck kinase-deficient variant of Jurkat cells and a specific Lck and Fyn tyrosine kinase inhibitor we found that enrichment of actin in raft patches is dependent on phosphotyrosine accumulation in the patches. These observations show a link between raft-mediated signaling and the interaction of actin cytoskeleton with raft membrane domains.
糖基磷脂酰肌醇(GPI)锚定蛋白和糖鞘脂的侧向交联可触发信号级联反应,从而导致淋巴细胞活化。关于信号如何通过质膜转导的一种可能解释源自细胞膜中筏状鞘脂 - 胆固醇微区的概念。GPI锚定蛋白、糖脂和其他筏成分的交联导致质膜中形成稳定的膜斑块,这些斑块富集了Src - 酪氨酸激酶家族的成员。我们研究了Jurkat T细胞系对筏斑块形成的细胞反应,特别是肌动蛋白细胞骨架的变化。我们发现由GPI锚定的CD59蛋白和神经节苷脂GM1形成的筏斑块积累丝状肌动蛋白。最有趣的是,我们观察到筏斑块中有大量酪氨酸磷酸化蛋白积累,有力地支持了它们可作为信号转导中心发挥作用的观点。使用Jurkat细胞的Lck激酶缺陷变体以及特定的Lck和Fyn酪氨酸激酶抑制剂,我们发现筏斑块中肌动蛋白的富集依赖于斑块中磷酸酪氨酸的积累。这些观察结果表明筏介导的信号传导与肌动蛋白细胞骨架与筏膜结构域之间的相互作用存在联系。