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Untitled - D Ank Unlimited

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FcμR 267 Fc receptors on human T cells<br />

Peptides<br />

pFc´<br />

F(ab´) 2<br />

Pepsin<br />

digestion<br />

comprised of two C terminal heavy chain segments<br />

(C H2, C H3) and a portion of the hinge region linked by the<br />

central disulfide bond and noncovalent forces. This 50-kDa<br />

fragment is unable to bind antigen, but it has multiple<br />

other biological functions, including complement fixation,<br />

interaction with Fc receptors on cell surfaces, and placental<br />

transmission of IgG. One Fc fragment is produced by<br />

papain digestion of each IgG molecule. The Fc region of an<br />

intact IgG molecule mediates effector functions by binding<br />

to cell surface receptors or C1q complement protein.<br />

FcμR<br />

IgM Fc receptors have been described but remain to be<br />

well characterized.<br />

Fc piece<br />

Refer to Fc fragment.<br />

Fc receptor<br />

A structure on the surfaces of some lymphocytes, macrophages,<br />

or mast cells that specifically binds the Fc region<br />

of immunoglobulin, often when the Fc is aggregated.<br />

Effector cells express isoforms FcαcR, FcγR, or FcεR and<br />

activate signaling that mediates receptor-mediated endocytosis,<br />

phagocytosis, and ADCC in addition to neutrophil<br />

and mast cell degranulation with the release of inflammatory<br />

mediators and cytokines. Numerous FcRs belong to the<br />

immunoglobulin (Ig) superfamily and contain ITAMs. The<br />

Fc receptors for immunoglobulin G (IgG) are designated<br />

FcγR. Those for IgE are designated FcεR. IgM and IgD<br />

Fc receptors have yet to be defined. Neutrophils, eosinophils,<br />

mononuclear phagocytes, B lymphocytes, selected T<br />

lymphocytes, and accessory cells bear Fc receptors for IgG<br />

on their surfaces. When the Fc region of immunoglobulin<br />

binds to the cation permease Fc receptor, there is an influx<br />

of Na + or K + that activates phagocytosis, H 2O 2 formation,<br />

and cell movement by macrophages.<br />

Fc receptors on human T cells<br />

Fc receptors (FcRs) are carried on 95% of human peripheral<br />

blood T lymphocytes. On about 75% of the cells, the FcRs<br />

are specific for immunoglobulin M (IgM); the remaining<br />

20% are specific for IgG. The FcR-bearing T cells are also<br />

designated T M and T G or Tμ and Tγ. The T M cells act as<br />

helpers in B cell function. They are required for the B cell<br />

responses to pokeweed mitogen (PWM). In cultures of B<br />

cells with PWM, the T M cells also proliferate, supporting<br />

the views on their helper effects. Binding of IgM to FcR of<br />

IgG<br />

Fc fragment.<br />

Papain<br />

digestion<br />

Fab<br />

Fc<br />

Fab<br />

Fc (IgG) receptor (neonatal).<br />

Fcε RI Fcε RII Fcα R<br />

Fcα and Fcε receptors.<br />

Fcγ RI Fcγ RII Fcγ RIII<br />

Fcγ receptors.<br />

T M cells is not a prerequisite for helper activity. In contrast<br />

to the T M cells, the T G cells effectively suppress B cell differentiation.<br />

They act on the T M cells, and their suppressive<br />

F

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