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Antigen presenting cell |
An antigen-presenting cell (APC) or accessory cell is a cell that displays foreign antigen complexed with MHC on its surface. T-cells may recognize this complex using their T-cell receptor (TCR).
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APCs fall into two categories: professional or non-professional.
Most cells in the body can present antigen to CD8+ T cells via MHC class I molecules and thus act as "APCs" however the term is often limited to those specialized cells that can prime T cells (i.e., activate a T cell that has not been exposed to antigen, termed a naive T cell). These cells, in general, express MHC class II as well as MHC class I molecules, and can stimulate CD4+ ("helper") cells as well as CD8+ ("cytotoxic") T cells.
To help distinguish between the two types of APCs, those that express MHC class II molecules are often called professional antigen-presenting cells.
These professional APCs are very efficient at internalizing antigen, either by phagocytosis or by receptor-mediated endocytosis, and then displaying a fragment of the antigen, bound to a class II MHC molecule, on their membrane. The T cell recognizes and interacts with the antigen-class II MHC molecule complex on the membrane of the antigen-presenting cell. An additional co-stimulatory signal is then produced by the antigen-presenting cell, leading to activation of the T cell.
There are three main types of professional antigen-presenting cell:
A non-professional APC does not constitutively express the Major histocompatibility complex proteins required for interaction with naive T cells; these are expressed only upon stimulation of the non-professional APC by certain cytokines such as IFN-γ. Non-professional APCs include:
After the APCs phagocytose pathogens, they usually migrate via vast networks of lymph vessels to arrive at draining lymph nodes (this network is collectively known as the Lymphatic system). The lymph nodes become a collection point to which APCs such as dendritic cells can interact with T cells. They do this by chemotaxis: which involves interacting with Chemokines that are expressed on the surface of cells (eg. endothelial cells of the high endothelial venules) or have been released as chemical messengers to draw the APCs to the lymph nodes. During the migration, DCs undergo a process of maturation; in essence, they lose most of their ability to further engulf pathogens, and they develop an increased ability to communicate with T cells. Enzymes within the cell digest the swallowed pathogen into smaller pieces containing epitopes, which are then presented to T cells using MHC.
Recent research indicates that only certain epitopes of a pathogen are presented because they are immunodominant, possibly as a function of their binding affinity to the MHC. The stronger binding affinity allows the complex to remain kinetically stable long enough to be recognized by T cells.
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This article does not cite any references or sources. Please help improve this article by adding citations to reliable sources. Unverifiable material may be challenged and removed. (November 2008) |
Some books mention activated T cells as Antigen Presenting Cells. There is no theoretical proof to back this yet. T cells don't express MHC II on their surface, nor are they known to process exogenously-derived proteins, so they most likely don't act as professional antigen presenting cells. However, like all other nucleated cells, they express MHC I, which allows them to present endogenous antigen to CD8 (Cytotoxic) T cells, which makes them non-professional antigen presenting cells. The language can be confusing, so some authorswho? use APC to refer only to professional APC, and leave out the phrase 'non-professional APC' altogether when discussing nucleated cells presenting endogenous antigen in MHC I.
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