Semple J W, Szewczuk M R
Clin Immunol Immunopathol. 1986 Oct;41(1):116-29. doi: 10.1016/0090-1229(86)90056-5.
The Natural Killer (NK) activity in the thymus and NK-sensitive thymocyte targets of dystrophic mice was investigated. Dystrophic and normal mouse thymocytes or spleen cells were layered on discontinuous Percoll gradients (5 or 10% increments, respectively) between 40 and 70% and centrifuged at 1700 g for 30 min. All fractions were tested for either NK activity or used a 51Cr-labeled NK-sensitive targets in a 6-hr 51Cr release assay. The density interface between the 50% (1.060 g/ml) and 60% (1.075 g/ml) Percoll fractions of either dystrophic or normal mouse spleen cells and the 40% (1.050 g/ml) and 50% (1.060 g/ml) Percoll fractions of either dystrophic or normal mouse thymocytes were found to contain the largest proportion of NK activity using YAC-1 lymphoma tumor cells as targets. In addition, the NK activity in dystrophic mouse spleen cells and thymocytes was significantly greater when compared with normal mouse controls. Target binding cell studies revealed that these Percoll fractions of dystrophic mouse spleen cells and thymocytes had greater numbers of conjugate-forming cells when compared with normal control groups. Cell depletion experiments using either anti-Thy 1.2, anti-asialo-GM 1 or anti-NK-1 plus complement treatment revealed that the cell responsible for NK activity in the 50% Percoll fraction interface of dystrophic mouse spleen cells was asialo-GM 1 positive. NK-1 positive, and partially Thy 1.2 positive. However, the cells displaying NK-activity in the thymus of normal or dystrophic mice were found to be highly Thy-1.2 positive and peanut agglutinin (PNA) negative. The density interface between the 60% (1.075 g/ml) and 65% (1.081 g/ml) Percoll fractions of either normal or dystrophic mouse thymocytes contained the largest proportion of NK-sensitive target cells. Interestingly, the 60% Percoll fraction of dystrophic mouse thymocyte targets was significantly more susceptible to NK-mediated lysis than that of the normal mouse thymocyte population. Cell depletion experiments revealed that the NK-sensitive thymocyte population was similar in both mice, that is, Thy-1.2 positive, cortisone sensitive, PNA positive, Dolichos biflorus (DBA) negative and asialo GM-1 negative. The results indicate that there are density differences between splenic and thymic NK cells. In addition, there are density and phenotypic differences between thymic NK cells and thymic NK-sensitive target cells. The findings support the hypothesis that there are different populations of NK cells.
对营养不良小鼠胸腺中的自然杀伤(NK)活性以及NK敏感的胸腺细胞靶标进行了研究。将营养不良和正常小鼠的胸腺细胞或脾细胞铺在40%至70%之间的不连续Percoll梯度(分别以5%或10%递增)上,以1700 g离心30分钟。对所有组分进行NK活性测试,或在6小时的51Cr释放试验中使用51Cr标记的NK敏感靶标。发现以YAC-1淋巴瘤肿瘤细胞为靶标时,营养不良或正常小鼠脾细胞的50%(1.060 g/ml)和60%(1.075 g/ml)Percoll组分之间的密度界面以及营养不良或正常小鼠胸腺细胞的40%(1.050 g/ml)和50%(1.060 g/ml)Percoll组分中含有最大比例的NK活性。此外,与正常小鼠对照组相比,营养不良小鼠脾细胞和胸腺细胞中的NK活性显著更高。靶标结合细胞研究表明,与正常对照组相比,营养不良小鼠脾细胞和胸腺细胞的这些Percoll组分具有更多形成共轭的细胞。使用抗Thy 1.2、抗去唾液酸GM1或抗NK-1加补体处理的细胞清除实验表明,在营养不良小鼠脾细胞的50%Percoll组分界面中负责NK活性的细胞是去唾液酸GM1阳性、NK-1阳性且部分Thy 1.2阳性。然而,发现在正常或营养不良小鼠胸腺中显示NK活性的细胞高度Thy-1.2阳性且花生凝集素(PNA)阴性。正常或营养不良小鼠胸腺细胞的60%(1.075 g/ml)和65%(1.081 g/ml)Percoll组分之间的密度界面含有最大比例的NK敏感靶细胞。有趣的是,营养不良小鼠胸腺细胞靶标的60%Percoll组分比正常小鼠胸腺细胞群体对NK介导的裂解更敏感。细胞清除实验表明,两种小鼠中NK敏感的胸腺细胞群体相似,即Thy-1.2阳性、对可的松敏感、PNA阳性、双花扁豆(DBA)阴性且去唾液酸GM-1阴性。结果表明脾NK细胞和胸腺NK细胞之间存在密度差异。此外,胸腺NK细胞和胸腺NK敏感靶细胞之间存在密度和表型差异。这些发现支持了存在不同NK细胞群体的假设。