Abstract
Killing of virally infected cells or tumor cells by cytotoxic T lymphocytes requires targeting of lytic granules to the junction between the CTL and its target. We used whole-cell patch clamp to measure the cell capacitance at fixed intracellular [Ca2+] to study fusion of lytic granules in human CTLs. Expression of a fluorescently labeled human granzyme B construct allowed identification of lytic granule fusion using total internal reflection fluorescence microscopy. In this way capacitance steps due to lytic granule fusion were identified. Our goal was to determine the size of fusing lytic granules and to describe their behavior at the plasma membrane. On average, 5.02 ± 3.09 (mean ± s.d.) lytic granules were released per CTL. The amplitude of lytic granule fusion events was ~ 3.3 fF consistent with a diameter of about 325 nm. Fusion latency was biphasic with time constants of 15.9 and 106 seconds. The dwell time of fusing lytic granules was exponentially distributed with a mean dwell time of 28.5 seconds. Fusion ended in spite of the continued presence of granules at the immune synapse. The mobility of fusing granules at the membrane was indistinguishable from that of lytic granules which failed to fuse. While dwelling at the plasma membrane lytic granules exhibit mobility consistent with docking interspersed with short periods of greater mobility. The failure of lytic granules to fuse when visible in TIRF at the membrane may indicate that a membrane-confined reaction is rate limiting.
Highlights
The killing of virally infected cells or tumor cells by cytotoxic T lymphocytes (CTLs) is the basis for the adaptive cellular immune response [1]
Capacitance measurements combined with total internal reflection fluorescence (TIRF) microscopy were carried out in 38 CTLs to identify the capacitance steps associated with lytic granules (LGs) fusion
Combined patch-clamp recording and TIRF microscopy allowed us to identify capacitance steps associated with fusion of mature LGs in human CTLs
Summary
The killing of virally infected cells or tumor cells by cytotoxic T lymphocytes (CTLs) is the basis for the adaptive cellular immune response [1]. This process requires the release of cytotoxic substances from lytic granules (LGs) via exocytosis at a CTL-target cell contact area, the immunological or immune synapse (IS) [2]. LGs express the lysosomal membrane markers LAMP1 and LAMP2, contain proteolytic lysosomal enzymes and have an acidic lumenal pH [3]. LGs emerge from the endosomal/lysosomal compartment [7], and may result from the fusion of lysosomes with vesicles in which the cytotoxic proteins.
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