Borgers M, Verhaegen H, De Brabander M, Thoné F, van Reempts J, Geuens G
J Immunol Methods. 1977;16(2):101-10. doi: 10.1016/0022-1759(77)90045-x.
A procedure is described for the histochemical detection of purine nucleoside phosphorylase (PNP) activity in circulating lymphocytes of man. The number of PNP-positive cells, as evaluated on smears of Ficoll--Hypaque purified cells, correlated well with the number of E-rosette-forming cells of the same blood samples of healthy and diseased people with normal or abnormal numbers of E-rosettes. In healthy people, the number of PNP-positive cells was within the range of 70-80% of the total lymphocyte population, whilst the corresponding E-rosette-forming cells were scored between 60-75%. Patients with unusually low or high E-rosettes had equally low or high numbers of PNP-reactive cells. More substantial evidence for the presence of PNP activity in T-cells and not in B cells was gathered from experiments in which PNP activity and surface membrane immunoglobulins (SMIg) were simultaneously demonstrated on the same preparation. These results showed, on the one hand, that the bulk of lymphocytes that are reactive for PNP do not reveal SMIg and, on the other hand, that most Ig-bearing cells were unreactive for PNP.
本文描述了一种用于组织化学检测人循环淋巴细胞中嘌呤核苷磷酸化酶(PNP)活性的方法。在Ficoll - Hypaque纯化细胞涂片上评估的PNP阳性细胞数量,与健康人和患病人群相同血样中E花环形成细胞的数量密切相关,这些血样中E花环数量正常或异常。在健康人中,PNP阳性细胞数量占淋巴细胞总数的70 - 80%,而相应的E花环形成细胞比例为60 - 75%。E花环数量异常低或高的患者,其PNP反应性细胞数量同样低或高。通过在同一制剂上同时展示PNP活性和表面膜免疫球蛋白(SMIg)的实验,收集到了更多关于T细胞而非B细胞中存在PNP活性的有力证据。这些结果一方面表明,对PNP有反应的大部分淋巴细胞不显示SMIg,另一方面表明,大多数带有Ig的细胞对PNP无反应。