New insights into the regulation of ICAM-1 gene expression

References

• Rothlein R., Dustin M. L., Marlin S. D., Springer T. A. A human intercellular adhesion molecule (ICAM-1) distinct from LFA-1. J. Immunol. 1986; 137: 1270–1274
   PubMed Web of Science ®Google Scholar
• Marlin S. D., Springer T. A. Purified intercellular adhesion molecule-I (ICAM-1) is a ligand for lymphocyte function-associated antigen 1 (LFA-1). Cell 1987; 51: 813–819
   PubMed Web of Science ®Google Scholar
• Makgoba M. W., Sanders M. E., Ginther-Luce G. E., Dustin M. L., Springer T. A., Clark E. A., Mannoni P., Shaw S. ICAM-1 is a ligand for LFA-1-dependent adhesion of B, T and myeloid cells. Nature 1989; 331: 86–88
   Web of Science ®Google Scholar
• Diamond M. S., Staunton D. E., Marlin S. D., Springer T. A. Binding of integrin Mac-I (CDI Ib/CD18) to the third immunoglobulin-like domain of ICAM-1 (CD54) and its regulation by glycosylation. Cell 1991; 65: 961–971
   PubMed Web of Science ®Google Scholar
• Springer T. A. Adhesion receptors of the immune system. Nature 1990; 346: 425–434
   PubMed Web of Science ®Google Scholar
• Wawryk S. O., Novotny J. R., Wicks I. P., Wilkinson D., Maher D., Salvaris E., Welch K., Fecondo I., Boyd A. W. The role of the LFA-1 fICAM-1 interaction in human leukocyte homing and adhesion. Immunol. Rev. 1989; 108: 135–161
   PubMed Web of Science ®Google Scholar
• Dustin M. L., Rothlein R., Bhan A. K., Dinarello C. A., Springer T. A. A natural adherence molecule (ICAM-1): induction by IL-1 and interferon-γ, tissue distribution, biochemistry and function. J. Immunol. 1986; 137: 245–254
   PubMed Web of Science ®Google Scholar
• Rothlein R., Czajkowski M., O'Neill M. M., Marlin S. D., Mainolfi E., Merluzzi V. J. Induction of intercellular adhesion molecule-I on primary and continuous cell lines by pro-inflammatory cytokines. J. Immunol. 1988; 141: 1665–1669
   PubMed Web of Science ®Google Scholar
• Pober J. S., Gimbrone M. A., Jr., Lapierre L. A., Mendrick D. L., Fiers W., Rothlein R., Springer T. A. Overlapping patterns of activation of human endothelial cells by interleukin-I, tumor necrosis factor, and immune interferon. J. Immunol 1986; 137: 1893–1896
   PubMed Web of Science ®Google Scholar
• Carlos T. M., Harlan J. M. Leukocyte-endothelial adhesion molecules. Blood 1994; 84: 2068–2102
   PubMed Web of Science ®Google Scholar
• Dustin M. L., Springer T. A. Role of lymphocyte adhesion receptors in transient interactions and cell locomotion. Annu. Rev. Immunol. 1991; 9: 27–66
   PubMed Web of Science ®Google Scholar
• Sligh J. E., Ballantyne C. M., Rich S. S., Hawkins H. K., Smith C. W., Bradley A., Beaudet A. L. Inflammatory and immune responses are impaired in mice deficient in intercellular adhesion molecule 1. Chem. Immunol. 1993; 90: 8529–8533
   Google Scholar
• Greve J. M., Davis G., Meyer A. M., Forte C. P., Yost S. C., Marlor C. W., Kamarck M. E., McClelland A. The major human rhinovirus receptor is ICAM-1. Cell 1989; 56: 839–847
   PubMed Web of Science ®Google Scholar
• Merluzzi V. J. D. E., Rothlein R., Barton R., Marlin S. D., Springer T. A. A cell adhesion molecule, ICAM-1, is the major surface receptor for rhinoviruses. Cell 1989; 56: 849–853
   PubMed Web of Science ®Google Scholar
• Berendt A. R., Simmons D. L., Tansey J., Newbold C. I., Marsh K. Intercellular adhesion molecule-I is an endothelid cell adhesion receptor for. Plasmodiumfalciparum. Nature 1989; 341: 57–59
   PubMed Web of Science ®Google Scholar
• Johnson J. P., Stade B. G., Holzmann B., Schwable W., Riethmuller G. Lk novo expression of intercellular adhesion molecule 1 in melanoma correlates with increased risk of metastasis. Proc. Natl. Acad. Sci. USA 1989; 86: 641–644
   PubMed Web of Science ®Google Scholar
• Moses H., Panek R. B., Benveniste E. N., Ting J. P.-Y. Usage of primary cells to delineate IFN–responsive DNA elements in the HLA-DRA promoter and to identify a novel IFN–enhanced nuclear factor. J. Immunol. 1992; 148: 3643–3651
   PubMed Web of Science ®Google Scholar
• Degitz K., Lian-Jie L., Caughman S. W. Cloning and characterization of the 5′-transcriptional regulatory region of the human intercellular adhesion molecule 1 gene. J. Biol. Chem 1991; 266: 14024–14030
   PubMed Web of Science ®Google Scholar
• Voraberger G., Schafer R., Stratowa C. Cloning of the human gene for intercellular adhesion molecule 1 and analysis of its 5′-regulatory region: induction by cytokines and phorbol ester. J. Immunol. 1991; 147: 2777–2786
   Web of Science ®Google Scholar
• Wertheimer S. J., Myers C. L., Wallace R. W., Parks T. P. Intercellular adhesion molecule-1 gene expression in human endothelial cells: differential regulation by tumor necrosis factor-a and phorbol myristate acetate. J. Biol. Chem. 1992; 267: 12030–12035
   PubMed Web of Science ®Google Scholar
• Lenardo M. J., Baltimore D. NK-κB: a pleiotropic mediator of inducible and tissue-specific gene control. Cell 1989; 58: 227–229
   PubMed Web of Science ®Google Scholar
• Montgomery K. F., Osbom L., Hession C., Tizard R., Goff D., Vassallo C., Tam P. I., Bomsztyk K., Lobb R., Harlan J. M., Pohlman T. H. Proc. Natl. Acad. Sci. USA 1991; 88: 6523–6527
   PubMed Web of Science ®Google Scholar
• Sachs A. B. Messenger RNA degradation in eukaryotes. Cell 1993; 74: 413–421
   PubMed Web of Science ®Google Scholar
• Schuler G. D., Cole M. D. GM-CSF and oncogene mRNA stabilities are independently regulated in trans in a mouse monocytic tumor. Cell. 1988; 55: 1115–1122
   PubMed Web of Science ®Google Scholar
• Shaw G., Kamen R. A conserved AU sequence from the 3′ untranslated region of GM-CSF mRNA mediates selective mRNA degradation. Cell 1986; 46: 659–667
   PubMed Web of Science ®Google Scholar
• Horley K. J., Carpenito C., Baker B., Takei F. Mdecular cloning of murine intercellular adhesion molecule (ICAM-1). EMBO J. 1989; 8: 2889–2896
   PubMed Web of Science ®Google Scholar
• Staunton D. E., Marlin S. D., Stratowa D., Dustin M. L., Springer T. A. Primary structuer of ICAM-1 demonstrates interaction between members of the immunoglobulin and intgrin supergene families. Cell 1988; 52: 925–933
   PubMed Web of Science ®Google Scholar
• Ohh M., Smith C. A., Carpenito C., Takei F. Regulation of intercellular adhesion molecule-I gene expression involves multiple mRNA stabilization mechanisms: Effects of interferon-y and phorbol myristate acetate. Blood 1994; 84: 2632–2639
   PubMed Web of Science ®Google Scholar
• Wager R. E., Assoian R. K. A phorbol ester-regulated ribonuclease system controlling transforming growth factor PI gene expression in hematopoietic cells. Mol. Cell. Biol. 1990; 10: 5983–5990
   PubMed Web of Science ®Google Scholar
• Yomom K., El-Hajjaoui Z., Koeffler H. P. Regulation of levels of IL-1 mRNA in human fibroblasts. J. Cell Physiol. 1989; 139: 610–616
   PubMed Web of Science ®Google Scholar
• Wodnar-Filipowicz A., Moroni C. Regulation of interleukin 3 mRNA expression in mast cells occurs at the posttranscriptional level and is mediated by calcium ions. Proc. Natl. Acad. Sci. USA 1990; 87: 777–781
   PubMed Web of Science ®Google Scholar
• Weber B., Horiguchi J., Luebbers R., Sherman M., Kufe D. Post-transcriptional stabilization of c-fms mRNA by a labile protein during human monocytic differentiation. Mol. Cell. Biol. 1989; 9: 769–775
   PubMed Web of Science ®Google Scholar
• Gillis P., Malter J. S. The adenosineuridine binding factor recognizes the AU-rich elements of cytokine. lymphokine, and oncogene mRNAs. J. Biol. Chem. 1991; 266: 3172–3177
   PubMed Web of Science ®Google Scholar
• Bohjanen R. P., Petryniak B., June C. H., Thompson C. B., Lindsten T. An inducible cytoplasmic factor (AU-B) binds selectively to AUUUA multimers in the 3′ untranslated region of lymphokine mRNA. Mot. Cell. Bio. 1991; 11: 3288–3295
   Web of Science ®Google Scholar
• Ohh M., Takei F. Interferon-yand phorbol myristate acetate-responsive elements involved in intercellular adhesion molecule-1 mRNA stabilization. J. Biol. Chem. 1994; 269: 30117–30120
   PubMed Web of Science ®Google Scholar
• Bevilacqua M. P., Pober J. S., Mendrick D. L., Cotran R. S., Gimbrone M. A. ldentification of an inducible endothelial-leucocyte adhesion molecule. Proc. Natl. Acad. Sci. USA 1987; 84: 9238–9242
   PubMed Web of Science ®Google Scholar
• Staunton D. E., Dustin M. L., Springer T. A. Functional cloning of ICAM-2, a cell adhesion ligand for LFA 1 homologous to ICAM-1. Nature 1989; 339: 6164
   Web of Science ®Google Scholar
• Xu H., De Fougerolles Tong I. L., Springer T. A. A. R. Isolation, characterization, and expression of mouse ICAM-2 complementary and genomic DNA. J. Immunol. 1992; 149: 2650–2655
   PubMed Web of Science ®Google Scholar
• DeFougerolles A. R., Stacker S. A., Schwarting R., Springer T. A. Characterization of ICAM-2 and evidence for a thii counter-receptor for LFA-1. J. Exp. Med. 1991; 174: 253–267
   PubMed Web of Science ®Google Scholar
• Fawcett J., Holness C. L. L., Needham L. A., Turley H., Gatter K. C., Mason D. Y., Simmons D. L. Molecular cloning of ICAM-3, a third ligand for LFA-1, constitutively expressed on resting leukocytes. Nature 1992; 360: 481–484
   PubMed Web of Science ®Google Scholar
• Vazeux R., Hoffman P. A., Tomita S. K., Dickinson E. S., Jasman R. L., John T., St., Gallatin M. W. Cloning and characterization of a new intercellular adhesion molecule ICAM-R. Nature 1992; 360: 485–488
   PubMed Web of Science ®Google Scholar
• Jackson R. J. Cytoplasmic regulation of mRNA function: The importance of the 3′ untranslated region. Cell 1993; 74: 9–14
   PubMed Web of Science ®Google Scholar
• Ohh M., Takei F. Regulation of ICAM-1 mRNA stability by cycloheximide: Rde of serindthreonine phosphorylation and protein synthesis. J. Cell. Biochem. 1995, in press
   PubMed Web of Science ®Google Scholar