Martorell J, Rojo I, Vilella R, Martinez-Caceres E, Vives J
Servei Immunologia, Hospital Clinic i Provincial de Barcelona, Spain.
J Immunol. 1990 Sep 1;145(5):1356-63.
CD27 mAb recognize a disulfide-linked homodimer of 55 kDa present in the majority of T cells and in a minor subpopulation of thymocytes. Although an increase of CD27 expression has been described in activated T cells, this Ag is poorly expressed in long term growing T cells. It has been also reported that CD27- becomes CD27+ upon activation. In the aim to better know the relationship between CD27 expression and the activation and maturation processes, the induction of this Ag in thymocytes was analyzed. The results obtained in this work show that: 1) CD27 is expressed only in thymocytes with high CD3 Ag density. 2) Its expression can be induced in low density CD3 CD4+ CD8+ cells by Con A and in low CD3 Ag density by PMA+ionomycin. 3) PMA alone or in combination with rIL-2 induces CD25 and CD71 expression but not CD27. 4) Unlike CD27, the Ag CD45RA, CD26, and CD76, which are present only in a minor thymocyte subpopulation, are not induced in double positive thymocytes. Because it has been reported that cyclosporin A interferes with thymocytes maturation and blocks the transition from double to single positive cells, its effect was measured on CD27 induction. Cyclosporin A did not inhibit CD25 expression induced by both Con A and PMA+ionomycin, but under these conditions it inhibited the induction of CD27. In this paper we discuss whether CD27 could be implicated in T cell maturation.
CD27单克隆抗体识别一种55 kDa的二硫键连接的同型二聚体,其存在于大多数T细胞和少数胸腺细胞亚群中。尽管已报道活化T细胞中CD27表达增加,但该抗原在长期生长的T细胞中表达较低。也有报道称CD27 -细胞在活化后变为CD27 +细胞。为了更好地了解CD27表达与活化和成熟过程之间的关系,分析了胸腺细胞中该抗原的诱导情况。这项工作获得的结果表明:1)CD27仅在CD3抗原密度高的胸腺细胞中表达。2)其表达可通过刀豆蛋白A在低密度CD3 CD4 + CD8 +细胞中诱导,通过佛波酯+离子霉素在低CD3抗原密度下诱导。3)单独的佛波酯或与重组白细胞介素-2联合使用可诱导CD25和CD71表达,但不诱导CD27表达。4)与CD27不同,仅存在于少数胸腺细胞亚群中的抗原CD45RA、CD26和CD76在双阳性胸腺细胞中不被诱导。因为有报道称环孢素A干扰胸腺细胞成熟并阻断从双阳性到单阳性细胞的转变,所以测定了其对CD27诱导的影响。环孢素A不抑制刀豆蛋白A和佛波酯+离子霉素诱导的CD25表达,但在这些条件下它抑制CD27的诱导。在本文中,我们讨论了CD27是否可能与T细胞成熟有关。