chapter 7 major histocomptibility complex (mhc). processing and presentation of exogenous and...

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Chapter 7 Major Histocomptibility Complex (MHC)

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Page 1: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Chapter 7 Major Histocomptibility Complex (MHC)

Page 2: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Processing and presentation of exogenous and endogenous antigens

Page 3: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Antigenic peptides recognized by T cells form trimolecular complexes with a TCR and an MHC molecule

Class I MHC

Peptide CD8

TCR

TC cell

peptide

Page 4: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

TCR and MHC-peptide

TCR

peptide

MHC

Page 5: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

1. MHC molecules act as antigen-presenting structure.2. MHC molecules expressed by an individual influence the repertoire of antigens to which t

hat individual’s TH cells and TC vells can respond.

3. MHC partly determines the response of an individual to antigens of infectious organisms.

4. MHC has been implicated in the susceptibility to disease and in the development of autoimmunity.

Page 6: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

本章大綱 :

1. General Organization and Inheritance of the MHC 2. MHC Molecules and Genes 3. Genomic Map of MHC Genes 4. Cellular Distribution of MHC Molecules 5. Regulation of MHC Expression 6. MHC and Immune Responsiveness 7. MHC and Disease Susceptibility

Page 7: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

General Organization and Inheritance of the MHC

Page 8: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Gorer (1930s):

1. Rejection of foreign tissue is the result of an immune response to cell-surface molecules.

2. Identification of I, II, III and IV groups of genes.

Gorer and Snell (1940s & 1950s):

1. Antigens encoded by the genes in the group II took part in the rejection of transplanted tumors and other tissues.

2. Snell called these genes “histocompatibility genes” (currently called H-2 genes)

3. Snell was awarded the Nobel Prize in 1980.

Page 9: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Human MHC: human leukocyte antigen (HLA) Mouse MHC: H-2

Page 10: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class I MHC:- Expressed on the surface of nearly all nucleated cells; the major

function of the class I gene products is presentation of peptide

Ags to CD8+ T cells.

Class II MHC:- Expressed primarily on Ag-presenting cells (macrophages,

dendritic cells, and B cells), where they present processed

antigenic peptides to CD4+ T cells.

Class III MHC:- Generally encode various secreted proteins that have immune

functions, including components of the complement system and

molecules involved in inflammation.

Page 11: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens
Page 12: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

- The MHC loci are polymorphic: Many alternative forms of the gene, or alleles, exist at each locus.

- The MHC loci are closely linked. The recombination frequency within the H-2 complex is only 0.5%.

- Most individuals inherit the alleles encoded by these closely linked loci as two sets, one from each parent. Each set of alleles is referred to as a haplotype.

- The MHC alleles are codominantly expressed; that is, both maternal and paternal gene products are expressed in the same cells.

Page 13: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens
Page 14: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Inheritance of MHC haplotypes

Page 15: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Acceptance or rejection of skin grafts is controlled by the MHC type of the inbred mice

Page 16: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Inheritance of HLA haplotype in a hypothetical human family

Page 17: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Congenic MHC mouse strain

- Inbred mouse strains are syngeneic or identical at all genetic loci.

- Two strains are congenic if they are genetically identical except at a single locus or region.

- Congenic strains can be produced by a series of crosses, backcrosses, and selections.

Page 18: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Production of congenic mouse strain

Strain A.B

Genetically identical to strain A except for the MHC locus or loci contributed by strain B.

Page 19: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Examples of recombinant congenic mouse strains generated during production of the B10.A strain from parental

strain B10 (H-2b) and parental strain A (H-2a)

Page 20: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

MHC Molecules and Genes

Page 21: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class I molecule

(12 kDa)

(45 kDa)

Page 22: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class II MHC molecule

(28 kDa) (33 kDa)

Page 23: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class I and class II molecules

Page 24: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class I chain, class II , chains and 2M are members of the Ig superfamily

Page 25: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

3-D structure of the external domains of a human class I HLA molecule based on x-ray crystallog

raphic analysis

Page 26: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Cleft: 25Å x 10Å x 11Å

can bind a peptide of 8-10 a.a.

Page 27: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Superimposition of the peptide-binding cleft of class I and class II MHC molecules

Red: HLA-A2 (Class I) blue: HLA-DR1 (Class II)

Page 28: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Organization of class I MHC gene

= K

Page 29: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Organization of class II MHC gene

IA IA

= IA

= IA

Page 30: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Peptide binding by MHC molecules

- Peptide binding by class I and class II molecules does not exhibit the fine specificity characteristic of Ag binding by Ab and TCR.

- A given MHC molecule can bind numerous different peptides, and some peptides can bind to several different MHC molecules.

- The binding between a peptide and an MHC molecule is often referred to as “promiscuous” ( 雜亂的 ).

Page 31: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Peptide-binding cleft is blocked at both ends in class I molecules

8 – 10 amino acid residues, most commonly 9

Page 32: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Peptide-binding cleft is open at both ends in class I molecules

13 – 18 amino acid residues

Page 33: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Binding affinity of MHC to peptides

- The association constant KD of the peptide-MHC molecule complex is approximately 10-6.

- The rate of association is low, but the rate of dissociation is even lower.

- Thus, the peptide-MHC molecule association is very stable under physiological conditions and most of the MHC molecules expressed on the membrane of a cell are associated with a peptide of self or nonself origin.

Page 34: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class I MHC molecules bind peptides and present them to CD8+ T cells

– cytosolic or endogenous processing pathway

Page 35: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Anchor residues in nonameric (9) peptides eluted from two class I MHC molecules

Usually hydrophobic

Page 36: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Vesicular stomatitis Sendai virus virus (VSV-8) peptide (SEV-9) nucleo- protein

Two different nonamers can bind to the same H-2kb

Page 37: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Conformational difference in bound peptides of different lengths

Page 38: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Molecular models based on crystal structure of an influenza virus antigenic peptide and an endogenous

peptide bound to a class I MHC molecule

influenza virus endogenous

Page 39: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

1 and 2 domains of HLA-B27 and a bound antigenic peptide

peptide water molecule

Page 40: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class II MHC molecules bind peptides and present them to CD4+ T cells

– endocytic or exogenous processing pathway

Page 41: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Peptide-binding cleft is open at both ends in class I molecules

A central core of 13 a.a. determines the ability of a peptide to bind class II.

13-18 a.a. residues

Page 42: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens
Page 43: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Polymorphism of class I and class II molecules

- The diversity of the MHC within a species stems from polymorphism, the presence of multiple alleles at a given genetic locus within the species.

- The MHC possesses an extraordinarily large number of different alleles at each locus and is one of the most polymorphic genetic complexes known in higher vertebrates. HLA-A 60 alleles H-2K 55 alleles HLA-B 110 alleles H-2D 60 alleles HLA-C 40 alleles

- The theoretical diversity possible for the mouse is: 100 (K) x 100 (IA) x 100 (IA) x 100 (IE) x 100 (IE) x 100 (D) = 1012

Page 44: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Linkage disequilibrium

Certain allelic combinations occur more frequently than predicted is referred to as linkage disequilibrium.

[Hypothesis]:

1. Sufficient numbers of generations have not elapsed. 2. Certain combinations of alleles are beneficial to the individuals. 3. Crossovers are more frequent in certain DNA sequence regions than in others.

Page 45: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Variability in the amino acid sequence of allelic class I MHC molecules

Page 46: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Location of polymorphic amino acid residues

Most of the residues with significant polymorphism are located in the peptide-binding cleft

Page 47: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Class III molecules are not membrane proteins, are not related structurally to class I and class II molecules, and have no role in Ag presentation, although most play some role in immune responses.

e.g., C2, C4a, C4b, factor B, 21-hydroxylase enzymes, TNFTNFheat shock proteins (HSP)

Page 48: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Genetic Map of MHC Genes

Page 49: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Mouse H-2 is on the chromosome 17

Class IClass I Nonclassical Nonclassical Class IIClass II Class IIIClass III Class I Class I Nonclassical Nonclassical

Page 50: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Human HLA is on the chromosome 6

Class IIClass II Nonclassical Nonclassical Class IIClass II Class IIIClass III Class IClass I Nonclassical Nonclassical

Page 51: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Cellular Distribution of MHC Molecules

Page 52: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Cellular distribution of MHC class I molecules

- In general, the classical MHC class I molecules are expressed on most somatic cells.

- The highest level of class I molecules are expressed on lymphocytes: 1 % of the total plasma membrane proteins or 5 x 105 molecules / cell.

- Fibroblasts, muscle cells, hepatocytes and neural cells express very low levels of class I molecules.

- A few cell types (e.g., neurons and sperm cells at certain stages of differentiation) appear to lack class I MHC molecules altogether.

Page 53: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Cellular distribution of MHC class II molecules

- Class II molecules are expressed constitutively only by Ag-presenting cells (APC), e.g., macrophages, dendritic cells, and B cells.

- Thymic epithelial cells and some other cell types can be induced to function as APC and then express class II molecules under certain conditions.

Page 54: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Various MHC molecules expressed on APC of a heterozygous H-2k/d mouse

Page 55: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

Nonclassical MHC class I and class II molecules

- Structurally similar to class I or class II molecules

- Less polymorphic

- Expressed at lower level

- Tissue distribution is more limited

- Functions not clear

Page 56: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens
Page 57: Chapter 7 Major Histocomptibility Complex (MHC). Processing and presentation of exogenous and endogenous antigens

The End