Cesarman-Maus G, Cantu-Brito C, Barinagarrementeria F, et al. secretion. Together, these findings suggest an emerging, multifaceted role for annexin A2 in human health and disease. The author’s work has been inspired by numerous colleagues and mentors, and by the author’s grandfather, and former ACCA member, Dr. J. Burns up Amberson. INTRODUCTION The annexins constitute a family of more than 60 highly conserved, Ca2+-regulated, phospholipid-binding proteins that have existed for more than 500 million years (1). Humans express 12 annexins (annexins A1-A11 and A13), and, among these, annexin A2 (A2) is usually arguably the most extensively investigated with respect to health and disease (2,3). Common annexins consist of a 30- to 35-kilodalton core domain made up of four alpha helical, Ca2+-binding annexin repeats, and a more hydrophilic amino-terminal tail domain name, which is essentially unique to each family member. Through their capacity for Ca2+-dependent membrane binding, annexins add or annex proteins to membrane surfaces and also facilitate membrane fusion events. These properties allow the annexins to fulfill a wide variety of intra- and extracellular functions, and the term annexinopathy has come to reflect their newly acknowledged roles in human pathophysiology (4). ANNEXIN A2 AND ITS PARTNER PROTEINS In the last 20 years, it has become progressively obvious that this cell surface is usually a major site for protease assembly and activity (5,6). In Batyl alcohol the 1980s, however, the concept that human endothelial cells could assemble components of the fibrinolytic system was novel. Our research began with the observation that human endothelial cells reacted specifically with antibodies directed against plasminogen and its tissue activator (tissue plasminogen activator, tPA) (7,8). Ligand blotting of a plasma membrane portion isolated from human endothelial cell homogenates revealed that both plasminogen and tPA interacted specifically with a 36-kilodalton protein expressed around the cell surface (9). The purified protein bound both plasminogen and tPA in a dose-dependent and high-affinity manner, and amino acid sequencing recognized this cell surface protein as annexin A2 (10). We now know that A2 is usually synthesized by endothelial cells, monocytes, macrophages, dendritic cells, trophoblast cells, epithelial cells, and some tumor cells, and can exist either as a soluble monomer in the cytoplasm, or as Batyl alcohol a complex associated with cellular membranes (11,12). The S100 family consists of low molecular excess weight (9- to 14-kilodalton) dimeric proteins that undergo structural shifts in response to changes in Ca++ concentration, and often interact with annexins (13). By forming a heterotetrameric complex with protein S100A10, A2 increases its sensitivity to Ca++ and its ability to bind to cellular membranes at resting intracellular Ca++ concentrations (14). S100A10 is unique among the family of S100 proteins in that it exists in a permanent calcium-on state, and does not require a Ca++-induced conformational switch to associate with annexin A2 (15). Crystallographic studies have revealed that, in the tetrameric (A2?S100A10)2 complex, two copies of S100A10 are linked non-covalently to create a molecular groove, which is occupied by Batyl alcohol the -helical N-terminal 14 amino acids of A2. In endothelial cells, S100A10 is usually stabilized by this conversation with A2, which masks a polyubiquitination site that would normally destine unpartnered S100A10 for degradation within the proteasome (16). Three additional family members, S100A4, S100A6, and S100A11, have been reported to bind A2 gene are associated with increased risk of stroke (47,48), whereas additional SNPs have been associated with elevated risk of avascular necrosis of bone (osteonecrosis) (49). In acute promyelocytic leukemia, which, conversely, is usually associated with life-threatening hemorrhage Batyl alcohol at the time of presentation (50), there is typically robust expression of A2 in leukemic blast cells (51). The producing coagulopathy appears to reflect a combination of disseminated intravascular coagulation and hyperfibrinolysis, the latter evidenced by elevated fibrin degradation products, depletion of plasma fibrinogen, and consumption of alpha2-antiplasmin (51). In cultured acute promyelocytic leukemia?like cells, elevated steady state levels of A2 mRNA returned to normal after treatment with the therapeutic differentiating agent all-retinoic acid (51). Follow-up studies have confirmed these findings and shown that S100A10 is also elevated in these cells (52,53). ANNEXIN A2 IN PROLIFERATIVE RETINAL ANGIOPATHY In several models of stimulated postnatal angiogenesis, 1970;46:663?5. Courtesy of the New York Academy of Medicine. Dr. Amberson was elected to the American Clinical and Climatological Association (ACCA) in 1922 at the age of 32, and served as its Vice President in 1940 (69). His first publication in the ACCA Transactions was entitled Clinical Studies of the Healing of Tuberculosis: I. Absorption of Pulmonary Deposits, and exhibited the importance of correlating serial clinical and radiologic findings in the treatment of tuberculosis (70). This paper revealed that pulmonary tuberculosis can heal by resolution, in addition to fibrosis and calcification, the more commonly acknowledged modes of healing. Rabbit polyclonal to PITPNM2 In his ACCA Memorial to J. Burns up Amberson, Dr. George W. Wright explained him as a scholarly, gentle persona teacher par.