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B cell is a type of lymph cell that is the footing for the organic structure ‘s humoral immune system ; it is produced from the root cell in the bone marrow ( Darling, 2010 ) . On its production a ego regenerating haematopoietic root cells give rise to lymphoid and myeloid primogenitor.

Looking chiefly at lymphoid primogenitor, it gives rise to B cell primogenitor, T cell primogenitor and Natural Killer cells ( Kuby et al. 2007, p.25 ) . Lymphoid primogenitor produces primogenitor B cells ; it is the earliest identifiable cell that ‘s committed to the development in the B cell lineage. The cells moves and rearrange their Ig heavy concatenation familial sections to do a functional IgH cistron that are expressed as pre B cell receptors.

The B cell receptor is a membrane bound antibody molecule. From the pre B cell receptor, some of the cells stays in the bone marrow and some moves into secondary lymphoid variety meats and there they reproduce, besides in the secondary lymphoid organs the cells undergo antigen dependent ripening. On the subject of B cell primogenitor, it produces B cell and these B cells further undergo two stages of ripening: an antigen independent stage and an antigen dependent stage ( Kempert, 2010 ) .

During the development, each B cell is genetically programmed or a procedure known as cistron translocation, to show a alone B cell receptor. The molecules of that B cell receptor are topographic point on its surface where it can respond with antigenic determinants of an antigen ( Kaiser, 2010 )

Antigenic determinants are antigenic determiners recognized and bound with B cell receptors and they are located on the surface of the antigen ( Austin, 2010 ) . There are known to be two chief categories of B cell antigenic determinants, one is Linear or uninterrupted, the surface that are interacted with the antibody are located following to each other consecutive on the protein. The 2nd 1 is assembled or discontinuous ; the constituents are located on disparate parts of the protein which are brought conformationally near to each other through side concatenation interactions ( ProImmune, 2010 ) .

Produced B cells contain two types of B lymph cells, Plasma cells and memory cells which express CD19, CD20 and CD21 on these cells ( Kempert, 2010 ) . Plasma cells are a type of white blood cell that produces antibodies. Once produced, B cells chiefly stay within the bone marrow and delay until an antigen invades the organic structure. The antigens bind to the B cell and excite it to organize plasma cells.

Plasma cells are known to hold characteristic looking karyon ; cytol that contains heavy unsmooth endoplasmic Reticulum and which is the site where antibodies are combined and besides a typical perinuclear Golgi composites where the antibody molecules are converted to their concluding signifiers and ready for secernment ( Abbas et al. 2009, p. 22 ) .

Memory cells are produced by antigen stimulation of naive B cells, they have proteins that are expressed on their surface that distinguish them from B cells and Plasma cells and they can last in a functionally province for many old ages after the antigen has been eliminated and besides they are known as B cell bomber types that are formed after an initial infection ( Abbas et al. 2009, p. 22 ) .


The major map of B cell is the secernment of antibodies. When an antigen has invades the organic structure and has been encountered by the immune system, they bind to B cell and a figure of certain B lymph cell are so stimulated and undergo cell division to bring forth plasma cell and memory cells which is known as clonal enlargement.

Clonal enlargement is a procedure that when a naive B cell brush a pathogen ‘s antigen. As the antigen floats through the blood system it gets attaches and binds to the naive B cells. This trigger clonal enlargement and the B cells multiples ( Kuby et al. 2007, p.17 ) .

The B cell receptors are the 1s responsible to adhere to the antigens, the delimited antigen is so engulfed into the B cell by the receptor mediated endocytosis. The antigen are digested and broken down into little fragments and displayed on the cell surface that ‘s sitting inside a category II Histocompatibility molecule.

With the aid of Helper T cells that binds with B cells, the B cells so secretes lymphokines that stimulates the B cells to travel through a cell rhythm that develops and turn the B cells from being B cell receptors to being a plasma cell that secrete antibodies ( Kimball, 2010 ) .

The plasma cell each produces a peculiar antibody that ‘s specifically attached to a specific antigen and these plasma cells are secreted into the blood system. As a particular antibody has attached to a specific antigen, the antibodies produce a humoral response and demobilize the pathogen, and do it easier to removal from the organic structure ( Anglin, 2010 ) . Once this procedure has occurred significance one time the organic structure defence has encountered and destroyed the pathogen ‘s antigen, the organic structure retrieve this pathogen ‘s antigen and this memory procedure is referred to as Memory cell.

Memory cells are produced by stirred B cells, they are the signifier of footing for long term unsusceptibility and responsible for secondary response. Equally shortly as an infection that was antecedently destroyed by the humoral immune system returns the memory cells that has remain hibernating produce a speedy response and the infection is removed as rapidly and efficaciously go forthing the patient immune ( Martin, 2010 ) .

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