Giurisato Emanuele, McIntosh Deirdre P, Tassi Maristella, Gamberucci Alessandra, Benedetti Angelo
Dipartimento di Fisiopatologia e Medicina Sperimentale, Università degli Studi di Siena, Viale Aldo Moro No. 1, 53100-Siena, Italy.
J Biol Chem. 2003 Feb 28;278(9):6771-8. doi: 10.1074/jbc.M210758200. Epub 2002 Dec 22.
The constitutive/inducible association of the T cell receptor (TCR) with isolated detergent-resistant, lipid raft-derived membranes has been studied in Jurkat T lymphocytes. Membranes resistant to 1% Triton X-100 contained virtually no CD3epsilon, part of the TCR complex, irrespective of cell stimulation. On the other hand, membranes resistant either to a lower Triton X-100 concentration (i.e. 0.2%) or to the less hydrophobic detergent Brij 58 (1%) contained (i) a low CD3epsilon amount (approximate 2.7% of total) in resting cells and (ii) a several times higher amount of the TCR component, after T cell stimulation with either antigen-presenting cells or with phytohemagglutinin. It appeared that CD3/TCR was constitutively associated with and recruited to a raft-derived membrane subset because (i) all three membrane preparations contained a similar amount of the raft marker tyrosine kinase Lck but no detectable amounts of the conventional membrane markers, CD45 phosphatase and transferrin receptor; (ii) a larger amount of particulate membranes were resistant to solubilization with 0.2% Triton X-100 and Brij 58 than to solubilization with 1% Triton X-100; and (iii) higher cholesterol levels were present in membranes resistant to either the lower Triton X-100 concentration or to Brij 58, as compared with those resistant to 1% Triton X-100. The recruitment of CD3 to the raft-derived membrane subset appeared (i) to occur independently of cell signaling events, such as protein-tyrosine phosphorylation and Ca(2+) mobilization/influx, and (ii) to be associated with clustering of plasma membrane rafts induced by multiple cross-linking of either TCR or the raft component, ganglioside GM(1). We suggest that during T cell stimulation a lateral reorganization of rafts into polarized larger domains can determine the recruitment of TCR into these domains, which favors a polarization of the signaling cascade.
在Jurkat T淋巴细胞中,研究了T细胞受体(TCR)与分离出的抗去污剂、源自脂筏的膜的组成型/诱导型结合。对1% Triton X-100具有抗性的膜几乎不含TCR复合物的一部分CD3ε,无论细胞是否受到刺激。另一方面,对较低浓度的Triton X-100(即0.2%)或疏水性较低的去污剂Brij 58(1%)具有抗性的膜,在静息细胞中含有少量的CD3ε(约占总量的2.7%),在用抗原呈递细胞或植物血凝素刺激T细胞后,TCR成分的含量会增加几倍。似乎CD3/TCR与源自脂筏的膜亚群组成型结合并被募集到该亚群,原因如下:(i)所有三种膜制剂中脂筏标记物酪氨酸激酶Lck的含量相似,但未检测到传统膜标记物CD45磷酸酶和转铁蛋白受体的含量;(ii)与用1% Triton X-100溶解相比,更多的颗粒膜对0.2% Triton X-100和Brij 58的溶解具有抗性;(iii)与对1% Triton X-100具有抗性的膜相比,对较低浓度的Triton X-100或Brij 58具有抗性的膜中胆固醇水平更高。CD3募集到源自脂筏的膜亚群似乎:(i)独立于细胞信号事件发生,如蛋白酪氨酸磷酸化和Ca(2+)动员/内流;(ii)与TCR或脂筏成分神经节苷脂GM(1)的多次交联诱导的质膜脂筏聚集有关。我们认为,在T细胞刺激过程中,脂筏横向重组为极化的更大结构域可决定TCR募集到这些结构域,这有利于信号级联反应的极化。