129809647049742500_115Introduction to b-lymphocytes (HE dyed) 1 b-lymphocytes called b cells. Derived from the bone marrow stem cells. Poultry is a development build in the Bursa, also known as SAC-dependent lymphocytes (Bursa dependent lymphocyte)/dependent lymphocytes called b cells in bone marrow, are made of bone marrow hematopoietic stem cellsDevelopment and differentiation. Compared with the t-lymphocytes, its slightly larger size. This lymphocyte Antigen stimulation, proliferation and differentiation of a large number of plasma cells. Plasma cells and synthesis and secretion of antibodies circulating in the blood. B-cell lymphoma is the most common type of Lymphocytic Leukemia, about study on the emergence of this disease. In bone marrow of mammals are in the thylakoid structure in organizationsFertility. Also known as dependent on lymphocytes in bone marrow. From bone marrow stem cells or b cells, after moving into the Bursa SAC organs or class, progressive differentiation potential of immune b cells. Mature b cells in peripheral blood to move out into the spleen, lymph nodes, and summary are mainly located in the spleen, spleen-cable and cable and gastrointestinal submucosal lymph nodules and Lymphoma lymph nodules, after Antigen stimulation,Proliferation of plasma cells, synthesis of antibodies, play to the function of humoral immunity. Most vaccines are being used by stimulating this type of b lymphocytes produce antibodies. B cells in the bone marrow, and lymph nodes in the collection number of t-cells, in less than the number of t cells in the blood and lymph nodes, thoracic duct is less, only a few participate in recycling. B cell membrane has manyDifferent signs, major surface antigen and surface receptors.��These flags are combined with huge protein molecules in the cell membrane. B1 cells t cell-independent cells. T-cell-dependent cell B2. B cells in vivo survival time is short, only a few days to a few weeks, but its memory cell can persist in the body. Summary of mammalian b cells differentiationDifferentiation can be divided into the former b-cells, b cell immature, mature b cells, activating b cells and plasma cells in five stages. Where b cells and immature b cell differentiation Antigen non-trusted, the differentiation made in the bone marrow. Antigen-dependent phase refers to the mature b cells in Antigen-stimulated activation after and continues to differentiate into plasma cells of the synthesis and secretion of antibodies, theStage in differentiation of primarily peripheral immune organs. B cells (pre-Bcell) b before spraying plant cells from bone marrow stem cell differentiation, and only exists in the bone marrow and fetal liver hematopoietic tissue. B cell cytoplasm detected IgM heavy chain in supply chain, but the light chain-free, has no surface expression of the Ig, therefore lack of reaction to the Antigen.End of Deoxy-nucleotide transferase (Terminal Deoxy nucleotidyl transferase TdT) and common acute lymphoblastic leukemia Antigen (common acute lymphoblastic leukaemia Antigen CALLA), CD10 expression in b cell, enter the immature b cells after both of these signs disappear, TdT and CD10 differentiated b cells and b-cells very useful at other stages. CD19, CD20, and expression of MHC �� Antigen begin at this stage. B cells against the Yuan before answering. Immature b cells (immatuRe b cell) began expressing mIgM unless combined with Antigen, the negative answer, b cells into a depressed state, cannot continue to differentiate into mature b cells, this is one of the formation mechanism of immune tolerance. CD19
SWTOR CD-key, CD20, and immature b cells increase expression of MHC �� Antigen, and may begin to express CD21�� Mature b cells (cell matrue b) mature in the bone marrow blood b cells migrate to the peripheral Lymphoid organs, simultaneous mIgM and mIgD,mIgD expression of membrane surface prevents the combination of b-cells and antigen expression induced immune tolerance. Mature b cells express complement receptor 1 (CR1), mitogen-induced by receptorAnd many other cytokine receptors. Activated b cells (activated b cell) mature b cell Antigen and Polyclonal stimulating agents become activated b cells after stimulation, broken and proliferation and differentiation, in this process, membrane binding Ig
level gradually reduced, gradually increased secretory Ig, there can be genes of immunoglobulin heavy chain class conversion�� Part of the activated b cells can differentiate into small lymphocytes, stopping proliferation and differentiation, and can survive for a few months to a few years, when you contact with the same antigen again, fast activation and differentiation occur, antibody incubation period is short, high
levels of antibodies, to maintain for a long time, the b cells called memory b cells (memory b cell). Plasma cells (plasmA cell PC) also known as antibody-secreting cells (the antibody secreting cell). Accepted after Antigen stimulation of mature b cells, antigen presenting cells, and aided by Th cells become activated b cells, which differentiate into plasma cells, synthesis and secretion of immunoglobulin, while also gaining PC-1 (plasmA cell Antigen-1) plasma cell-specific flags, and mIg,MHC Class �� antigens, CD19, CD20, CD21, mark disappears. Development survey of birds in place Bursa is the differentiation of b cells. Mammalian embryos, yolk sac is the first part of b cell differentiation, since then in the spleen and bone marrow, after the birth of theDifferentiation and maturation in the bone marrow. B-cell differentiation process can be divided into two phases, that is, antigens and antigen-dependent phase-independent period. Non-dependent Antigen, b-cell differentiation and antigens stimulation unrelated to take place mainly in Central immune organs. Antigen-dependent refers to a mature b cell after Antigen stimulation may continue to stage of differentiation for the synthesis and secretion of antibodies against plasma cells, primarily in the peripheral immuneWithin the organ. Early b cell proliferation and differentiation of bone marrow microenvironment, its happening and bone marrow hematopoietic microenvironment (hemopoietic inductive microenviroment HIM) are closely related. HIM is a hematopoietic stromal cells outside of the cell (stroma cell) and its fineExtracellular matrix and cell factor (extracellular matrix ECM). Stromal cells including macrophages, endothelial cells, fibroblasts and preadipocytes, fat cells, and so on. By interstitial cells secrete fibronectin, laminin, collagen and extracellular matrix formation, as well as synthesis and secretion of a number ofCytokines. HIM mainly through cytokine regulation of proliferation and differentiation of hematopoietic cells through adhesion to the hematopoietic cells and stromal cells in direct contact with each other, positioned in favour of hematopoietic cells mature and move out of the cell. B-cells in the development of b cells in the bone marrow and other blood cells, differentiation of stem cells in the bone marrow. View tCommon lymphoid stem cells and b cells may come from, but on the differentiation of radical ways, differentiation of position and its specific surface markers are not yet clear, pending further study. Proved that development of b cells within the bone marrow, can go through progenitor b cells (pro-B), b-cell (pre-B), immature b cells (immature b) and mature b cells(Mature) stage. Release of mature b cells to lymphocytes in peripheral lymphoid tissues, form b-cell library, after Antigen stimulation at this stage may continue to differentiate into plasma cells of the synthesis and secretion of antibodies, antigen-dependent differentiation. B the main stages in the differentiation of cells within the bone marrow changes to rearrangements of the immunoglobulin genes and expression of membrane surface markers.B-cell development and differentiation in the process, also experienced selection to remove non-functional gene rearrangement self reactive b cells and b cells to form mature peripheral b cells. 1. This early development of b-cell progenitor b cells, occurs in human embryo around the 9th week, starting around the 14th day of mice. Not express b-cell surface markers of specific, norLG gene rearrangement, still in the germline gene (germline) stage.
Progenitor of b cells with advanced b-specific flags may appear, Thy-1, Tdt, B200, MB-1, and so on. 2. B cells are progenitor differentiation of b cells, and accounted for 5% of adult bone marrow nucleated cells. B cells to check out is the earliest sign of LGHeavy chain gene rearrangement, then can be detected in the cytoplasmic IgM heavy chain of molecules, that is, supply chain.
Free light chain gene rearrangement, and therefore no expression of membrane Ig. But before the mouse b cells, cloned before two b-cell-specific genes, and c gamma and gamma v with homologous, named lambda 5 and Vpre-B genes, respectively, in front of the people have proven this gene is present in b cells.They encode non-Covalent protein Vpre-B and lambda 5, form a pseudo-light chain (chain �� pseudo l l) or replace the light chain (surrogate l chain). This pseudo-l chain and supply chain to form �� heavy chain and pseudo-l chain complexes and constitute its expression in b cell membrane receptors, and signaling about, the formerFurther differentiation of b cells play an important role. This phase also expression of MHC ��, Tdt, CD19, CD10, differentiation Antigen CD20 and CD24. CD19, CD20, and CD22 appears in the cytoplasm are early in the supply chain.
B cells against the original no answer, no immune function.
3. Immature b cells in this orderL-chain gene rearrangement, IgM molecules to form complete, and expressed in the film surface (IgM), �� may be called b cells. This kind of cell and Antigen binding, easy to make membrane receptor Crosslinking, negative signals, the b cells in a frustrated State, cannot continue to differentiate into mature b cells. This may lead to miscarriage of self reactive b cells cloned, is the formation of fine bOne of the mechanisms of cell self-tolerance. Immature b cells begin to lose Tdt and CD10, but expression of CD22, CD21 and FcR.
And CD19, CD20, and MHC Class �� molecules expression increases. 4. With further differentiation of b cells mature b cells, developing into mature b cells, and leave the bone marrow into the peripheral immune organs. ThisMembrane surface can be expressed when sIgM and sIgD, but the v zone the same, c district, so the identification of Antigen specific is the same.
Mature b-cell molecular changes can occur in a number of films, flag can be expressing various other films, such as the mitogen-receptor, complement receptors, Fc receptors, cytokine receptors, receptor, as well as other differentiation Antigen of the virus. 5.Plasma cells (PC) mature b cells in peripheral lymph BA accepted Antigen stimulation, with the help of TH cell and antigen-presenting cells, and under the action of cytokines may b cell activation, proliferation and differentiation for the synthesis and secretion of antibodies against plasma cells. This stage gradually lost membrane molecules such as CD19 b cells and CD22. And Ig classConversion, convert from IgM to Igg, IgA or IgE b cell. During this stage differentiation, there is some b cells can be recovered as small lymphocytes, and to stop the proliferation and differentiation, SIgD may disappear, and long life, can survive for a few months to a few years. When you contact with the same antigen again ease of activation and differentiation, so call this kind of memory b cells cells, andAgain the immune response of the body. When you mature b cells differentiate into plasma cells, b cell surface signs disappear, and there have been some new signs unique to plasma cells, such as plasma cell Antigen-1 (PCA-1). A plasma cells can produce only one category of Ig molecule, and loss of ability to produce other types. Plasma cell long life short, its lifetimeJust a few days, then died. Film reviews a variety of surface molecules on the surface of b cells, subjects to recognize antigens, immune cells and interactions between immune molecules, is the important basis for separation and identification of b cells. B principal cell surface molecules are leucocyte differentiation Antigen and MHC as well as a variety of membrane surface receptor. CD antigens important CD on b cell surface antigens, And b cell recognition and adhesion, b lymphocyte activation CD molecules related to the structure and function. Some CD of b cell Antigen monoclonal antibody identification and detection
Diablo 3 CD-KEY, scale, the number of different b cell differentiation and function of State. Major Antigen tissue compatibility complex (MHC) b cells not only MHCI antigen expression and expressionHigher proportion and density of MHC �� Antigen. In addition to plasma cells, b cells to activate b cells express MHC Class �� antigens. MHC �� Antigen on the surface of b cells in patients with b-cell and t-cell interaction plays an important role when, in addition, is also involved in b cell as the supporting role of antigen presenting cell. B multiple types of membrane surface of membrane surface receptorReceptor. 1. surface immunoglobulin (surface membrane immunoglobulin mIg) this is a b-cell-specific antigen receptor, is also a major feature of b-cell markers. Immature b cells express mIgM, mature b cells also express mIgD, mIgM both expression and mIGD, mature b-cell surface mIgG, mIgA or mIgE. In b-cell differentiation during b cell cytoplasmic IgM heavy chain in supply chain, but not the mIgM; when immature b cells is development, supply chain disappeared in the cytoplasm, expression mIgM began on the cell membrane. In a single b cell surface of all Ig variable region VH is the same andVL genes encoding their unique combination of type and therefore Antigen specificity is the same. After Antigen stimulation of b cell mIgD soon wore off, and memory b cell surface mIgD does not exist. As the b-cell receptor (b cell receptor BCR) outside the mIgM, and Ig both �� and Ig beta polypeptide chain, named as CD79A and CD79b, together with the mIg formation complex of BCR. 2. complement receptor (complement receptor CR) b CR1 and membrane surface CD2. CR1 (CD
35) can be combined and complement C
3b and C4b
wow power leveling, so as to promote the activation of b cells. CD2 (CD21) ligand isC
3d,C
3d b, and b cell surface with CR2 may also regulate cell growth and differentiation.
3.EB virus receptor CR2 (CD21) EB virus receptor, the EB virus infection of selective b cell-related. EB virus infection in vitro b-cell, b-Cell Immortalization (immortlaized) constructed as b-cellsParent cell-like cell lines, and Immunology of human monoclonal antibody technology has significant value.
In the body, increased mononuclear cells of EB virus infection and contagious disease, Burkitt's lymphoma and nasopharyngeal carcinoma, disease-related. 4. America Lu Si mitogen induced by receptor split the original (poke weed mitogen PWM) on tMitosis cells and b cells are run. In mice, LPs (lipopolysaccharide LPS) are commonly used by mitogen. In addition CowanI strains of Staphylococcus aureus (Staphylococcus aureusstrain CowanI SAC) for containing goldStaphylococcus protein a (Staphylococcal protein ASPA), through stimulation in combination with mIg b cell proliferation.
In addition, soybean agglutinin (soybean agglutinin SBA) b cell lectin. 5. multiple cytokines regulating b cell cytokine receptor activation,Proliferation and differentiation through corresponding to the b cell surface cytokine receptors and the role of regulation. B cell cytokine receptor mainly include IL-1R, IL-2R, IL-4R, IL-5R, IL-6R, and IL-7R, and IL-11R, and IL-12R, and IL-1
3R, IL-14R, and IL-�� r, and IL-�� TGF-�� r and r, and so on.
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tag : SWTOR CD-key,Diablo 3 CD-KE,wow power leve