Figure 2
Figure 2. Sequence of events leading to cellular activation by β2GPI-antibody complexes. β2GPI is not recognized by pathologic anti-β2GPI antibodies in the circulation. When negatively charged, phospholipids become exposed, and β2GPI will bind to this surface and change conformation. This step exposes a cryptic epitope in domain I that is recognized by the pathologic antibodies. The antibody fixes β2GPI in this conformation, and the antibody–β2GPI complex can subsequently interact with several surface receptors, such as glycoprotein Ibα (GPIbα), LRP8, annexin A2, and several members of the TLR family (TLR2, -4, and -8). Because receptor and phospholipid binding are mutually exclusive, the β2GPI–antibody complex probably dissociates from the surface before it can interact with a surface receptor.

Sequence of events leading to cellular activation by β2GPI-antibody complexes. β2GPI is not recognized by pathologic anti-β2GPI antibodies in the circulation. When negatively charged, phospholipids become exposed, and β2GPI will bind to this surface and change conformation. This step exposes a cryptic epitope in domain I that is recognized by the pathologic antibodies. The antibody fixes β2GPI in this conformation, and the antibody–β2GPI complex can subsequently interact with several surface receptors, such as glycoprotein Ibα (GPIbα), LRP8, annexin A2, and several members of the TLR family (TLR2, -4, and -8). Because receptor and phospholipid binding are mutually exclusive, the β2GPI–antibody complex probably dissociates from the surface before it can interact with a surface receptor.

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