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Jay Unkeless

  • PROFESSORIAL LECTURER Medicine
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Research

Structure and function of receptors for IgG that are found on neutrophils, macrophages, and NK cells; events that occur following activation of these receptors and identification of the various proteins involved in the reactions.

Our group studies the structure and function of receptors for IgG (Fc[gamma]R) that are found on neutrophils, macrophages and NK cells. Fc[gamma]R's link the effector cells of the immune system to the production of IgG following an immune response. Fc[gamma]Rs on effector cells, following crosslinking by multivalent immune complexes, can trigger the secretion of superoxide, release of hydrolytic enzymes, synthesis of cytokines, and killing of sensitized target cells.\r\n\r\n

A major aim of the laboratory is to analyze signaling pathways leading from Fc[gamma]R activation (by crosslinking) to cell effector activity. In particular, we are interested in the signaling mechanisms of glycan-phosphatidyl inositol-anchored Fc[gamma]R IIIb, and with the architecture of Fc[gamma]RIIIb in the plasma membrane. We have recently observed that crosslinking Fc[gamma]RIIIb results in the co-capping of Fc[gamma]RIIa and in the rapid partition into the Fc[gamma]RIIIb cap of a lipid probe, dI-I, that is initially diffusely distributed in the plasma membrane. It is thus likely that GPI-anchored protein capping results in a lipid membrane domain with significantly different physical properties from the bulk membrane. The properties of these domains, and the proteins that associate with the capped Fc[gamma]RIIIb caps are under investigation.

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Following our interest in phagocytosis, we have derivsed a screen for proteins that bind inositol hexaphosphate (IP6) and have probed a recently constructed macrophage expression library with a multivalent complex consisting of biotinylated IP6 conjugated to 125I-BSA. We have identified a serine/threonine kinase reported to be expressed strongly in spermatids, where it associates with microtubule associated proteins. This kinase is likely to be involved with exocytic events. The proteins that interact with the kinase are being studied biochemically, and by yeast two-hybrid interaction analysis. We are also mapping the domain(s) of the protein that bind IP6, and have mapped 5' genomic clones for use in isolating a knockout mutant.

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We have developed a system for obtaining synchronous and maximal stimulation of macrophages by Fc[gamma]R ligation to glass, and are screening for transcripts activated by this stimulation. Initial efforts in this direction used differential display PCR (ddPCR), and resulted in the isolation of a protein that may play a role in control of deubiquitination. However, ddPCR is fraught with technical difficulties, and we are now revisiting this problem utilizing a recently developed subtractive hybridization/PCR protocol.

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Publications

Qu Z, Odin J, Glass JD, Unkeless JC. Expression and characterization of a truncated murine Fc gamma receptor. J Exp Med 1988; 167: 1195-1210.

Odin JA, Edberg JC, Painter CJ, Unkeless JC. Regulation of phagocytosis and [Ca2+]i flux by distinct regions of an Fc receptor. Science 1991; 254: 1785-1788.

Shen Z, Lin CT, Unkeless J. Correlations among tyrosine phosphorylation of Shc, p72syk, PLC-gamma1, and [Ca2+]i flux in FcgammaRIIA signaling. J Immunol 1994; 152: 3017.

Boros P, Odin JA, Chen J, Unkeless JC. Specificity and class distribution of Fc gamma receptor autoantibodies in patients with autoimmune disease. J Immunol 1994; 152: 302-306.

Lin CT, Shen Z, Boros P, Unkeless J. Fc receptor-mediated signal transduction. J Clin Immunol 1994; 14.

Ghirlando R, Keown MB, Mackay GA, Lewis MS, Unkeless J, Gould HJ. Stoichiometry and thermodynamics of the interaction between the Fc fragment of human IgG1 and its low-affinity receptor FcgammaRIII. Biochemistry 1995; 34: 13320.

Unkeless J, Shen Z, Lin C, DeBeus E. Function of human FcgammaRIIA and FcgammaRIIIB. Semin. Immunol 1995; 7: 37.

Zhang F, Odin JA, Shen Z, Lin CT, Unkeless JC, Jacobson K. Lateral mobility of Fc gamma RIIa is reduced by protein kinase C activation. FEBS Lett 1995; 376(1-2): 77-80.

Edberg JC, Lin CT, Lau D, Unkeless J, Kimberly RP. The Ca2+ dependence of human Fcgamma receptor-initiated phagocytosis. J Biol Chem 1995; 270: 22301.

Industry Relationships

Physicians and scientists on the faculty of the Icahn School of Medicine at Mount Sinai often interact with pharmaceutical, device and biotechnology companies to improve patient care, develop new therapies and achieve scientific breakthroughs. In order to promote an ethical and transparent environment for conducting research, providing clinical care and teaching, Mount Sinai requires that salaried faculty inform the School of their relationships with such companies.

Dr.Unkeless is not currently required to report Industry relationships.

Mount Sinai's faculty policies relating to faculty collaboration with industry are posted on our website at http://icahn.mssm.edu/about-us/services-and-resources/faculty-resources/handbooks-and-policies/faculty-handbook. Patients may wish to ask their physician about the activities they perform for companies.

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