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Review
.2017 Feb;74(3):399-408.
doi: 10.1007/s00018-016-2350-7. Epub 2016 Sep 1.

Preparing the lethal hit: interplay between exo- and endocytic pathways in cytotoxic T lymphocytes

Affiliations
Review

Preparing the lethal hit: interplay between exo- and endocytic pathways in cytotoxic T lymphocytes

Hsin-Fang Chang et al. Cell Mol Life Sci.2017 Feb.

Abstract

Cytotoxic T lymphocytes patrol our body in search for infected cells which they kill through the release of cytotoxic substances contained in cytotoxic granules. The fusion of cytotoxic granules occurs at a specially formed contact site, the immunological synapse, and is tightly controlled to ensure specificity. In this review, we discuss the contribution of two intracellular compartments, endosomes and cytotoxic granules, to the formation, function and disassembly of the immunological synapse. We highlight a recently proposed sequential process of fusion events at the IS upon target cell recognition. First, recycling endosomes fuse with the plasma membrane to deliver cargo required for the docking of cytotoxic granules. Second, cytotoxic granules arrive and fuse upon docking in a SNARE-dependent manner. Following fusion, membrane components of the cytotoxic granule are retrieved through endocytosis to ensure the fast, efficient serial killing of target cells that is characteristic of cytotoxic T lymphocytes.

Keywords: Correlative light and electron microscopy; Early endosomes; Late endosomes; Recycling endosomes; SNARE proteins; Total internal reflection fluorescence microscopy.

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Figures

Fig. 1
Fig. 1
Endosomal pathways.a Overview of the major endosomal pathways in mammalian cells. The plasma membrane with protein cargo is endocytosed and forms intracellular endocytic vesicles (EV). Those vesicles homotypically fuse with each other and subsequently fuse with early endosomes (EE). EE are major sorting compartments within the cell. Endocytosed material is sorted into tubular structures and bud off as recycling endosomes (RE) which migrate back to the plasma membrane and exocytose there. Moreover, a process starts in early endosomes which results in the formation of endosomal carrier vesicles (yellow). During retro- and anterograde connections to the trans-Golgi endosomal cargo, newly formed proteins are exchanged. By an ongoing production of endosomal carrier vesicles and RE, the EE changes its shape and molecular composition and becomes a late endosome (LE). Finally late endosomes fuse with lysosomes (Lys) in which the remaining cargo mainly localized in endosomal carrier vesicles (multivesicular body) is degraded by hydrolytic enzymes. In some cell types such as cytotoxic T lymphocytes, LE can produce lysosomal-related organelles (LRO) that, as secretory lysosomes, become released by regulated exocytosis. Specific cargo may be inserted into LRO via a transport pathway from trans-Golgi via LE to LRO.b Closeup of EE and LE with some important molecular components; early endosomal antigen 1 (EEA1), endosomal sorting complexes required for transport (ESCRT), small GTPases (Rab5, Rab7, Rab11), sorting nexin (SNX)
Fig. 2
Fig. 2
Maturation of cytotoxic granules. Maturation of cytotoxic granules (CG) starts at late endosomes (LE) by budding off of secretory lysosomes (here named “precursor or mature CG”). Granzymes are incorporated into this vesicle by an anterograde transport from the Golgi network to LE and finally to CG. How other components like perforin and membrane effector proteins are incorporated is largely unknown. A new and interesting hypothesis (components inside thedashed area) emphasizes a function of recycling endosomes (RE) for maturation of CG. Two additional fusion events were proposed. The first fusion occurs between an LE-derived vesicle carrying different Rab proteins (Rab7, Rab27) and other CG cargo and an EE-derived RE carrying Rab11 and Munc13-4. This fusion, which itself is Munc13-4 dependent, results in an intermediate named exocytic vesicle. This vesicle may then fuse with the LE-derived precursor CG to form a mature CG.Lys lysosome
Fig. 3
Fig. 3
Exocytosis of cytotoxic granules. Secretion of cytotoxic granules (CGs) is a sequential process requiring exocytosis of recycling endosomes (RE) as an initial step (1). Thereby REs deliver components of the exocytic machinery for CGs such as the SNARE-associated protein Munc13-4 and the SNARE protein syntaxin11 (STX11) (2). Together with further, currently unknown SNARE proteins, those components serve as a docking platform for cytotoxic granules and initiate CG fusion through Munc13-4-catalyzed SNARE complex formation (3)
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