Antigen presenting cell
Introduction
Individual is protected from
different type of pathogen with the help of immune system. with the help of
confocal microscope, we observe mechanism of immune system.
Antigen is defined as cell that is specialized cell
that is responsible to stimulate to immune system to fight against disease.
There are two types of antigen. Foreign antigen is produced from outside body
like infection of virus, bacteria and second type are autoantigen. Antigen
presentation cell has two subset professional antigen presenting cell and
amateur antigen presenting cell. Macrophage monocyte dendritic cell and b cell
are professional antigen presenting cell. Amateur antigen present cell like glial
cell pancreatic beta cell keratinocyte cell and thyroid gland act only in
special condition. First, we discuss antigen presenting cell
Antigen presenting cell
Monocyte and microphage
Foreign particles engulf by monocyte and microphages.
Microphage cell that presents in tissue and monocyte circulate with in blood.
Microphages are present in bone, connective tissue, and brain. Kupffer cell are
microphage that present in liver cell. Adaptive and innate immunity is
controlled by microphages. PAMP, Toll-like,
scavenger, and mannose receptors
bind with antigen to activate microphages
Dendritic cell
Dendritic cell was described by Steinmann 1973. These
are professional antigen cell that produce in bone marrow and part of lymphoid
and nonlymphoid tissue. Myeloid stem cell produces two type of dendritic population.
Follicular dendritic cell produces when one population migrate toward lymph
node. Second population present in non-lymph node and then change in to
interstitial dendritic cell. Dendritic cells are suitable for specific antigen
presentation These cell highly concentrated at place where microbe enter.
Presentation of T cell is processed by dendritic cell and microbe is captured
by dendritic cell. Dendritic cells have ability to move in tissue so they
stimulate lymph node.
Follicular dendritic cell
Lymph node germinal follicle are responsible in
production of follicular dendritic cell. Follicular dendritic cell perform
function to activate b cell and main immunological memory. Only FDCs dendritic
cell that does not participate in antigen presentation of T cell. FDCs cell produce
cytokines that is responsible for activation of B cell in plasma.
Interstitial Dendritic cell
Except brain and eye interstitial cell present in all
tissue. The function of these cell to detect foreign particle in body. IDC
present in skin in large quantity, skin contain 25% of Langerhans cell and 2- 3
% skin cell. Suprabasilar epidermis is a place
where immature Langerhans cell present and identified by cytoplasmic birbeck
granule when class 1 class 2 CD +4 and other receptor are expressed in response
of pathogen.
Plasmacytoid dendritic cell
These cell is like antibodies that secreted from
plasma cell and it is belief that production of these cell in lymphoid
progenitor. PDCs are present in lymph node like spleen, tonsil, and
blood. These cell activated against viral infection. When virus attack DNA of
viruses is capture by toll like receptors 7 and 9. When viral DNA is captured
PDCs activate alpha bd beta interferon. These interferon do not allow viral
cell to attack on other uninfectious cell.
B cell
T cell is presented by B cell. B cell has specific
antigen receptor that bind with antigen and then modified into antibodies.
Cross linking of BCR include antigen which is breakdown in cytoplasm and
presentation of T cell in context to class 2. B cell is less concentrated. For presentation of antigen B cell
concentration is 100 to 10000 time less concentrated than macrophage for
antigen presentation.
Presentation of exogenic antigen
Exogenic
antigen is breakdown on the path of endocyte and fill up on class MHC2
molecule. ClassMHC 2 molecule perform their mechanism in different way with
macrophage and B cell. Using different receptor like PAMPs and antibodies dendritic
cell bound with antigen. Phagocytic cell ingest opsonizes bacteria and antigen.
Pseudopodia is formed by invagination of membrane during re arrangement of
cytokinin. Pseudopodia surround material and ingest them; these material change
in internal vacuole. Foreign particle is engulfed by B cell using receptor
mediated response. Clathrin membrane is area where localization of B cell
receptor take place. When receptor bind with clathrin it helps calthrin to move
inward membrane and make vesical.
Process of recycle of clathrin completed after that B
receptor express on surface of cell and membrane bounded vesical change into
vacuole. Phagosome is name of vacuole in microphage and B cell. Phagosome
combined with lysozyme that has hydrolytic enzyme that remove material from
phagosome and phagosome called phagolysosome.
Dendritic cell and cancer vaccination
Tumor cells are not actively participated in immunity
as HLA move downward and antigen of tumor cell do not present to T cell.
Immunity against tumor cell is increased by using cross priming vaccine. Tumor
cell exerted from patient and then purified. Tumor cell and dendritic cell
combine in laboratory and heat up for several day. Complete tumor cell is
engulfed by dendritic cell and suitable presentation of class 2 molecule. DCs
in patient produce action in responses of tumor cell. Vaccine is produced
against tumor according to this concept. cancer is treated by using dendritic
cell vaccine.
MHC 1 antigen presentation
MHC 1 cell are mostly present in nucleated cell. MHC1
cell is composed of heterodimer of different kind of alpha chain that coupled
noncovalently with b-2 macroglobulin. It is nonpolymorphic. Alpha chain is
composed of three domain. Plasma membrane is crossed by alpha 3butalph 2 and
alpha 1 is responsible for antigen bonding cell. MHC1 is bounded with peptide
that are 8-10 amino acid in length and peptide anchor on MHC 1 molecule with
the help of amino acid that are present on specific position.
Endoplasmic reticulum produce MHC 1 molecule ‘s
peptide binding site. cytosol is responsible for production of all type of
protein. Proteosome are catalytic enzyme that degrade protein small peptide.
Proteome composed of 28 subunits that are cylindrical
structure and contain 4 ring and each ring has seven subunit. Innate immunity
release IFNs that is responsible in production of three type of proteosome
subunits when viral infection take place. Proteosome are produces peptides that
bind with MHC molecule when inflammation occur.
MHC
class II presentation
APCs,
such as dendritic cells (DC), B
cell and microphages express MHCII molecule. Protein change into peptide that
form binding with MHCII molecule. Alpha and beta chain are part of MHCII molecule,
combine in endoplasmic reticulum and invariant chain stabile it. Golgi
apparatuses transport invariant chain and MHCII molecule into different
compartment these compartment called Ii and MHCII compartment. Proteases
cathepsin L and cathepsin S has acidic pH, due to acidic pH these protease
activate and digest it invariant chain
Pathway of antigen presentation
Two pathway is used by immune system to remove
extracellular and intracellular antigen. Cytosol pathway is responsible for the
processing of endogenous antigen and present on membrane. endocytic pathway is
path that processed exogenic antigen and present it on membrane with molecule
of MHCII.
Two scientist Morrison and Braciale perform experiment
to show that presentation of peptide bond is done by MHCI and MHCII molecule
Two clone of cytotoxin T cell is used in research, molecule of class MHCI
make association with influenza hemagglutinin is recognized by one type of Tc
cell. Same antigen that makes association with MHCII molecule that is
recognized by atypic TC line cell. Expression of both MHCI and MHC II molecule
by target cell and these target cells heated these molecule with infectious influenza
virus or with those virus that are inactivated with the help of UV radiation (non-activated
viruses have antigen but they loss replication ability). Target cells are also
heated with class I and II restricted Tc cell for the determination of lysis of
target cells lysis Class I and II restricted Tc cell were heated together. In
result Tc cells of class II molecule provide response against target cell which
are treated with infectious or non-infectious. The class I restricted cells
provide response against those target cells which were treated with infectious
virus. Using emetine production of viral protein stop when class I restricted
cells treated with viral infection that cause stimulation of class II
restricted cell but no stimulation produces in class I restricted cells. When
chloroquine using in experiment endocytic process pathway has been blocked by
drug it stimulates class I restricted cell. These experiment show that exogenic
antigen associated with class MHCII molecule and endogenic antigen associated
with MHCII molecule.
Antigen presenting cell
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