Copyright © Philip M. Parker, INSEAD. Terms of Use.

| Domain | Definition |
Health | The genetic region which contains the loci of genes which determine the structure of the serologically defined (SD) and lymphocyte-defined (LD) transplantation antigens, genes which control the structure of the immune response-associated (Ia) antigens, the immune response (Ir) genes which control the ability of an animal to respond immunologically to antigenic stimuli, and genes which determine the structure and/or level of the first four components of complement. (references) |
Source: compiled by the editor from various references; see credits. | |
(From Wikipedia, the free Encyclopedia)
Certainly the best known genes in the MHC region are the subset that encodes cell-surface antigen-presenting proteins. In humans, these genes are referred to as human leukocyte antigen (HLA) genes, although people often use the abbreviation MHC to refer to HLA gene products. To disambiguate the usage, some of the biomedical literature uses Mhc to refer specifically to the HLA protein molecules and reserves MHC for the region of the genome that encodes for this molecule, however this convention is not consistently adhered to.
The most intensely studied HLA genes are the nine so-called classical Mhc genes: HLA-A, HLA-B, HLA-C, HLA-DPA1, HLA-DPB1, HLA-DQA1, HLA-DQB1, HLA-DRA, and HLA-DRB1. In humans, the MHC is divided into three regions: Class I, II, and III. The A, B, and C genes belong to MHC class I while the six D genes belong to class II.
Besides being scrutinized by immunologists for its pivotal role in the immune system, the MHC has also attracted the attention of many evolutionary biologists, due to the high levels of allelic diversity found within many of its genes. Indeed, much theory has been devoted to explaining why this particular region of the genome harbors so much diversity, especially in light of its immunological importance.
The classical Mhc molecules (also referred to as HLA molecules in humans) have a vital role in the complex immunological dialog that must occur between T cells and other cells of the body. At maturity, Mhc molecules are anchored in the cell membrane, where they display short polypeptides to T cells, via the T cell receptors (TCRs). The polypeptides may be "self," that is, originating from a protein created by the organism itself, or they may be foreign, originating from bacteria, viruses, pollen, etc. The overarching design of the MHC-TCR interaction is that T cells should ignore self peptides while reacting appropriately to the foreign peptides. Foreign peptides that provoke an immune response are termed antigens.
Interestingly, the immune system has another, equally important method to identify antigen: B cells with their membrane-bound antibodies, also known as B cell receptors (BCRs). However, while the BCRs of B cells can bind to antigens without much outside help, the TCRs of T cells require "presentation" of the antigen: this is the job of Mhc. It is important to realize that the vast majority of the time, Mhc are kept busy presenting self-peptides, which the T cells should appropriately ignore. A full-force immune response usually requires the activation of B cells via BCRs and T cells via the Mhc-TCR interaction. This duplicity creates a system of "checks and balances" and underscores the immune system's potential for running amuck and causing harm to the body (see autoimmune disorders.)
All Mhc molecules receive polypeptides from inside the cells they are part of and display them on the cell's exterior surface for recognition by T cells. However, there are major differences between MHC class I and II in the method and outcome of peptide presentation.
Introduction
Molecular biology of MHC proteins
Because class I Mhc is loaded with proteins found it the cytosol, it is the primary way for a virus-infected cell to signal to T cells. It interacts exclusively with CD8+ T cells (also known as cytotoxic T cell lymphocytes or CTLs). The fate of a virus-infected cell is almost always apoptosis, or programmed cell death, initiated by the CD8+ T cell. This response seems like "killing the messenger," but the messenger in this case is virally infected and probably represents a risk of contagion for neighboring cells.
Because class II Mhc is loaded with extracellular proteins, it is mainly concerned with presentation of extracellular pathogens (for example, bacteria that might be infecting a wound or the blood.) Class II molecules interact exclusively with CD4+ T cells (also known as helper T cell lymphocytes or HTLs). The helper T cells then help to trigger an appropriate immune response which may include localized inflammation and swelling due to recruitment of phagocytes or may lead to a full-force antibody immune response due to activation of B cells.
Source: adapted by the editor from Wikipedia, the free encyclopedia under a copyleft GNU Free Documentation License (GFDL) from the article "Major histocompatibility complex."
Crosswords: MAJOR HISTOCOMPATIBILITY COMPLEX |
| Specialty definitions using "MAJOR HISTOCOMPATIBILITY COMPLEX": Adenovirus E3 Proteins ♦ Genes, MHC Class I, Genes, MHC Class II ♦ Haplotypes, Histocompatibility Antigens ♦ Interleukin-4 ♦ Langerhans Cells ♦ Minor Histocompatibility Loci, Minor Lymphocyte Stimulatory Loci ♦ Receptors, Antigen, T-Cell. (references) |
Source: compiled by the editor from various references; see credits. |
| Domain | Title |
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Source: compiled by the editor from various references; see credits. | |
| Subject | Topic | Quote |
Health | Further indications that more than one gene is involved in MS susceptibility comes from studies of families in which more than one member has MS. Several research teams found that people with MS inherit certain regions on individual genes more frequently than people without MS. Of particular interest is the human leukocyte antigen (HLA) or major histocompatibility complex region on chromosome 6. HLAs are genetically determined proteins that influence the immune system. (references) | |
Source: compiled by the editor from ICON Group International, Inc.; see credits. | ||
| The following statistics estimate the number of searches per day across the major English-language search engines as identified by various trade publications. Hyperlinks lead to commercial use of the expression at Amazon.com. |
| Expression | Frequency per Day |
major histocompatibility complex | 7 |
| Source: compiled by the editor from various references; see credits. | |
| Language | Translations for "MAJOR HISTOCOMPATIBILITY COMPLEX"; alternative meanings/domain in parentheses. | ||||||||||||||||||||||
Danish | vigtigste vævsforenelighedskompleks, vævstypeantigen. (various references) | ||||||||||||||||||||||
Dutch | hoofd-histocompatibiliteitscomplex. (various references) | ||||||||||||||||||||||
Finnish | pääryhmä elin-ja kudossiirron vastaanottajan geeneistä,jotka kontrolloivat kudosten yhteensopivuutta,histokompatibiliteettiä,ja käynnistävät tarpeen mukaan siirrännäisen hylkimiseen johtavat reaktiot. (various references) | ||||||||||||||||||||||
French | complexe majeur d'histocompatibilité. (various references) | ||||||||||||||||||||||
German | Haupthistokompatibilitäts-Komplex. (various references) | ||||||||||||||||||||||
Greek | μείζον σύμπλεγμα ιστοσυμβατότητας. (various references) | ||||||||||||||||||||||
Italian | complesso maggiore di istocompatibilit . (various references) | ||||||||||||||||||||||
Pig Latin | ajormay istocompatibilityhay omplexcay complexo de histocompatibilidade major. (various references) complejo mayor de histocompatibilidad. (various references) major histocompatibility complex. (various references) | ||||||||||||||||||||||
| 1. Crosswords 2. Usage: Commercial 3. Quotations: Non-fiction 4. Expressions: Internet | 5. Translations: Modern 6. Bibliography |
Copyright © Philip M. Parker, INSEAD. Terms of Use.