Department of Biology, Biotechnical Faculty, University of Ljubljana, Večna pot 111, 1000 Ljubljana, Slovenia.
Proc Natl Acad Sci U S A. 2011 Dec 27;108(52):21016-21. doi: 10.1073/pnas.1107473108. Epub 2011 Dec 15.
The cytotoxic cell granule secretory pathway is essential for immune defence. How the pore-forming protein perforin (PFN) facilitates the cytosolic delivery of granule-associated proteases (granzymes) remains enigmatic. Here we show that PFN is able to induce invaginations and formation of complete internal vesicles in giant unilamellar vesicles. Formation of internal vesicles depends on native PFN and calcium and antibody labeling shows the localization of PFN at the invaginations. This vesiculation is recapitulated in large unilamellar vesicles and in this case PFN oligomers can be seen associated with the necks of the invaginations. Capacitance measurements show PFN is able to increase a planar lipid membrane surface area in the absence of pore formation, in agreement with the ability to induce invaginations. Finally, addition of PFN to Jurkat cells causes the formation of internal vesicles prior to pore formation. PFN is capable of triggering an endocytosis-like event in addition to pore formation, suggesting a new paradigm for its role in delivering apoptosis-inducing granzymes into target cells.
细胞毒性细胞颗粒分泌途径对于免疫防御至关重要。穿孔蛋白(PFN)如何促进颗粒相关蛋白酶(颗粒酶)的细胞质传递仍然是个谜。本文作者表明,PFN 能够在巨大单层囊泡中诱导凹陷和完整内部囊泡的形成。内部囊泡的形成依赖于天然 PFN 和钙离子,抗体标记显示 PFN 定位于凹陷处。这种囊泡化在大单层囊泡中得到重现,在此情况下,可以看到 PFN 寡聚体与凹陷的颈部相关联。电容测量表明,PFN 能够在没有孔形成的情况下增加平面脂质膜表面积,这与诱导凹陷的能力一致。最后,将 PFN 添加到 Jurkat 细胞中会在形成孔之前导致内部囊泡的形成。PFN 除了能够形成孔之外,还能够触发类似胞吞的事件,这表明其在将凋亡诱导颗粒酶递送到靶细胞中的作用有了新的范例。