Peters P J, Geuze H J, Van der Donk H A, Slot J W, Griffith J M, Stam N J, Clevers H C, Borst J
Laboratory of Cell Biology, Medical School, University Hospital, Utrecht, The Netherlands.
Eur J Immunol. 1989 Aug;19(8):1469-75. doi: 10.1002/eji.1830190819.
An ultrastructural analysis of human cytotoxic T lymphocyte-target cell (CTL-TC) interaction has been undertaken to enable a better understanding of the killing mechanism. Attention was focused on granules in the CTL, which are known to contain lethal compounds. Within the membrane-delimited cytotoxic granule an electron-dense core as well as numerous membrane vesicles were identified. In CTL-TC conjugates, specific membrane interactions take place, allowing the formation of intercellular clefts into which the granule cores and internal vesicles are released. T cell surface membrane molecules known to be involved in CTL-TC interaction (T cell receptor, CD3 and CD8) are present on the membranes of the granule cores and internal vesicles, facing outward. An explanation for this localization of the membrane may be found in the fact that the granule is connected with an endocytotic pathway. Moreover, the lumen of the granule is rich in the enzyme cathepsin D, which indicates an association with a lysosomal compartment. Exocytosed vesicles and cores are seen to adhere to the plasma membrane of the TC. Although the exact contents of the granule vesicles and core remain to be identified, we suggest that specific interaction of CTL membrane molecules on the cytolytic granule components with molecules on the plasma membrane of the TC may ensure the unidirectional delivery of the lethal hit.
为了更好地理解杀伤机制,对人细胞毒性T淋巴细胞-靶细胞(CTL-TC)相互作用进行了超微结构分析。研究重点放在CTL中的颗粒上,已知这些颗粒含有致死性化合物。在膜界定的细胞毒性颗粒内,鉴定出一个电子致密核心以及许多膜泡。在CTL-TC结合物中,发生了特异性膜相互作用,形成了细胞间裂隙,颗粒核心和内部囊泡被释放到其中。已知参与CTL-TC相互作用的T细胞表面膜分子(T细胞受体、CD3和CD8)存在于颗粒核心和内部囊泡的膜上,面向外侧。这种膜定位的一种解释可能在于颗粒与内吞途径相连这一事实。此外,颗粒腔富含组织蛋白酶D,这表明它与溶酶体区室有关。可见胞吐的囊泡和核心附着在靶细胞的质膜上。尽管颗粒囊泡和核心的确切成分仍有待确定,但我们认为,细胞溶解颗粒成分上的CTL膜分子与靶细胞质膜上的分子之间的特异性相互作用可能确保了致死性打击的单向传递。