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Open AccessJournal ArticleDOI

Cytotoxic T lymphocyte granules are secretory lysosomes, containing both perforin and granzymes.

TLDR
In this article, the subcellular localization of perforin, granzymes, and known endosomal and lysosomal marker proteins was determined in human and murine CTL, by immunogold labeling of ultrathin cryosections followed by electron microscopy.
Abstract
Cytotoxic T lymphocytes (CTL) contain granules that are exocytosed during specific interaction with target cells (TC). In this process, the granule contents, including the lethal protein perforin, as well as granzymes, a family of serine esterases, are delivered to the TC. Information regarding the routing of these proteins towards the granule and their exact localization within the granule is of primary importance to resolve the mechanism of granule-mediated TC killing. In this study, the subcellular localization of perforin, granzymes, and known endosomal and lysosomal marker proteins was determined in human and murine CTL, by immunogold labeling of ultrathin cryosections followed by electron microscopy. Perforin and granzymes can be detected in rough endoplasmic reticulum, Golgi complex, trans-Golgi reticulum, and in all cytotoxic granules. Within the granules, they have a similar distribution and are localized not only in the so-called dense core but also over the region containing small internal vesicles. This finding implies that perforin and granzymes can be released in membrane-enveloped and/or -associated form into the intercellular cleft formed upon CTL-TC interaction. On the basis of the present evidence, additional release of these molecules in soluble form cannot be excluded. The lysosomal membrane glycoproteins lamp-1, lamp-2, and CD63, are abundantly present on the granule-delimiting outer membrane, which becomes incorporated into the CTL plasma membrane during lethal hit delivery. In contrast, the cation-dependent mannose 6-phosphate receptor, known to be present in endosomes and absent from lysosomes, is found only in a minority of the granules. Together with our previous findings that the granules are acidic and connected to the endocytic pathway, these observations define CTL granules as secretory lysosomes.

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Citations
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Journal ArticleDOI

B lymphocytes secrete antigen-presenting vesicles.

TL;DR: It is demonstrated by immunoelectron microscopy that the limiting membrane of MIICs can fuse directly with the plasma membrane, resulting in release from the cells of internal MHC class II-containing vesicles, suggesting a role for exosomes in antigen presentation in vivo.
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Regulation of immune responses by extracellular vesicles

TL;DR: Given the tremendous therapeutic potential of extracellular vesicles, this Review focuses on their role in modulating immune responses, as well as their potential therapeutic applications.
Journal ArticleDOI

Sensitive and viable identification of antigen-specific CD8+ T cells by a flow cytometric assay for degranulation

TL;DR: A novel technique to enumerate antigen-specific CD8+ T cells using a marker expressed on the cell surface following activation induced degranulation, a necessary precursor of cytolysis, and CD107-expressing CD8+, expressing cognate T cell receptors (TCR), is presented.
Journal ArticleDOI

CD107a as a functional marker for the identification of natural killer cell activity

TL;DR: It is suggested that employing CD107a as a marker of NK cell functional activity may allow for the identification of a large fraction of activated NK cells that may degranulate in the absence of cytokine secretion.
Journal ArticleDOI

Exosomal-like vesicles are present in human blood plasma.

TL;DR: It is demonstrated that blood is a physiological fluid for exosome circulation in the body, suggesting their role in cell-cell or organ-organ communications as carriers for molecules that need to reach distant cell targets.
References
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Journal ArticleDOI

The Biogenesis of Lysosomes

TL;DR: Article de synthese sur les lysosomes: biogenese, definition, role biologique, Les enzymes lysOSomales sont decrites ainsi that leur role dans l'exo et l'endocytose.
Journal ArticleDOI

The trans Golgi Network: Sorting at the Exit Site of the Golgi Complex

Gareth Griffiths, +1 more
- 24 Oct 1986 - 
TL;DR: A model is proposed whereby three different classes of proteins are sorted into different vesicles in the last Golgi compartment, the trans Golgi network, which corresponds to a tubular reticulum on the trans side of the Golgi stack.
Journal ArticleDOI

The mannose 6-phosphate receptor and the biogenesis of lysosomes

TL;DR: It is proposed that the MPR/lgp-enriched structure is a specialized endosome (prelysosome) that serves as an intermediate compartment into which endocytic vesicles discharge their contents, and where lysosomal enzymes are released from the M PR and packaged along with newly synthesized lysOSomal glycoproteins into lyssomes.
Journal ArticleDOI

Segregation of MHC class II molecules from MHC class I molecules in the Golgi complex for transport to lysosomal compartments.

TL;DR: The intracellular distribution of MHC class I and class II molecules reflects the dichotomy in presentation of antigen from endogenous and exogenous origin, respectively.
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