A metalloproteinase disintegrin that releases tumour-necrosis factor-α from cells (original) (raw)
References
Rose-John, S. & Heinrich, P. C. Soluble receptors for cytokines and growth factors: generation and biological function. Biochem. J.300, 281–290 (1994). ArticleCAS Google Scholar
Walcheck, B. et al. Neutrophil rolling altered by inhibition of L-selectin shedding in vitro. Nature380, 720–723 (1996). ArticleADSCAS Google Scholar
Mohler, K. M. et al. Protection against a lethal dose of endotoxin by an inhibitor of tumour necrosis factor processing. Nature370, 218–220 (1994). ArticleADSCAS Google Scholar
Decker, T., Lohmann-Matthes, M. L. & Gifford, G. E. Cell-associated tumour necrosis factor (TNF) as a killing mechanism of activated cytotoxic macrophages. J. Immunol.138, 957–962 (1987). CASPubMed Google Scholar
Kriegler, M., Perez, C., De Fay, K., Albert, I. & Lu, S. D. A novel form of TNF/cachectin is a cell surface cytotoxic transmembrane protein: ramifications for the complex physiology of TNF. Cell53, 45–53 (1988). ArticleCAS Google Scholar
Bazzoni, F. & Beutler, B. The tumor necrosis factor ligand and receptor families. N. Engl. J. Med.334, 1717–1725 (1996). ArticleCAS Google Scholar
Sherry, B. & Cerami, A. Cachectin/tumor necrosis factor exerts endocrine, paracrine, and autocrine control of inflammatory responses. J. Cell Biol.107, 1269–1277 (1988). ArticleCAS Google Scholar
McGeehan, G. M. et al. Regulation of tumour-necrosis factor-α processing by a metalloproteinase inhibitor. Nature370, 558–561 (1994). ArticleADSCAS Google Scholar
Gearing, A. J. et al. Processing of tumour-necrosis factor-α precursor by metalloproteinases. Nature370, 555–557 (1994). ArticleADSCAS Google Scholar
Wolfsberg, T. G. & White, J. M. ADAMs in fertilization and development. Dev. Biol.180, 389–401 (1996). ArticleCAS Google Scholar
Black, R. A. et al. Relaxed specificity of matrix metalloproteinases (MMPs) and TIMP-insensitivity of tumor necrosis factor-α (TNF-α) production suggest the major TNF-α converting enzyme is not an MMP. Biochem. Biophys. Res. Commun.225, 400–405 (1996). ArticleCAS Google Scholar
Stocker, W. et al. The metzincins—topological and sequential relations between the astacins, adamalysins, serralysins, and matrixins (collagenases) define a superfamily of zinc-peptidases. Protein Sci.4, 823–840 (1995). ArticleCAS Google Scholar
Howard, L., Lu, X., Mitchell, S., Griffiths, S. & Glynn, P. Molecular cloning of MADM: a catalytically active mammalian disintegrin-metalloprotease expressed in various cell types. Biochem. J.317, 45–50 (1996). ArticleCAS Google Scholar
Cerretti, D. P. et al. Molecular cloning of the interleukin-1β converting enzyme. Science256, 97–100 (1992). ArticleADSCAS Google Scholar
Woessner, J. F. Jr Matrix metalloproteinases and their inhibitors in connective tissue remodeling. FASEB J.5, 2145–2154 (1991). ArticleCAS Google Scholar
Barr, P. J. Mammalian subtilisins: the long-sought dibasic processing endoproteases. Cell66, 1–3 (1991). ArticleCAS Google Scholar
Teeter, M. M., Roe, S. M. & Heo, N. H. Atomic resolution (0.83 A) crystal structure of the hydrophobic protein crambin at 130K. J. Mol. Biol.230, 292–311 (1993). ArticleCAS Google Scholar
Wolfsberg, T. G. et al. The precursor region of a protein active in sperm-egg fusion contains a metalloprotease and a disintegrin domain: structural, functional, and evolutionary implications. Proc. Natl Acad. Sci. USA90, 10783–10787 (1993). ArticleADSCAS Google Scholar
Yoshida, S., Setoguchi, M., Higuchi, Y., Akizuki, S. & Yamamoto, S. Molecular cloning of cDNA encoding MS2 antigen, a novel cell surface antigen strongly expressed in murine monocytic lineage. Int. Immunol.2, 585–591 (1990). ArticleCAS Google Scholar
Krätzschmar, J., Lum, L. & Blobel, C. P. Metargidin, a membrane-anchored metalloprotease-disintegrin protein with an RGD integrin binding sequence. J. Biol. Chem.271, 4593–4596 (1996). Article Google Scholar
Yagami-Hiromasa, T. et al. A metalloprotease-disintegrin participating in myoblast fusion. Nature377, 652–656 (1995). ArticleADSCAS Google Scholar
Weskamp, G., Krätzschmar, J., Reid, M. S. & Blobel, C. P. MDC9, a widely expressed cellular disintegrin containing cytoplasmic SH3 ligand domains. J. Cell. Biol.132, 717–726 (1996). ArticleCAS Google Scholar
McMahan, C. J. et al. A novel IL-1 receptor, cloned from B cells by mammalian expression, is expressed in many cell types. EMBO J.10, 2821–2832 (1991). ArticleCAS Google Scholar
Peschon, J. J. et al. Early lymphocyte expansion is severely impaired in interleukin 7 receptor-deficient mice. J. Exp. Med.180, 1955–1960 (1994). ArticleCAS Google Scholar
Mortensen, R. M., Conner, D. A., Chao, S., Geisterfer-Lowrance, A. A. & Seidman, J. G. Production of homozygous mutant ES cells with a single targeting construct. Mol. Cell. Biol.12, 2391–2395 (1992). ArticleCAS Google Scholar
Dexter, T. M., Allen, T. D. & Lajtha, L. G. Conditions controlling the proliferation of haemopoietic stem cells in vitro. J. Cell. Physiol.91, 335–344 (1976). Article Google Scholar
Snell, W. J. & White, J. M. The molecules of mammalian fertilization. Cell85, 629–637 (1996). ArticleCAS Google Scholar
Libby, P., Alroy, J. & Pereira, M. E. A neuraminidase from Trypanosoma cruzi removes sialic acid from the surface of mammalian myocardial and endothelial cells. J. Clin. Invest.77, 127–135 (1986). ArticleCAS Google Scholar
Warner, S. J. & Libby, P. Human vascular smooth muscle cells. Target for and source of tumor necrosis factor. J. Immunol142, 100–109 (1989). CASPubMed Google Scholar
Meier, T., Arni, S., Malarakannan, S., Poincelet, M. & Hoessli, D. Immunodetection of biotinylated lymphocyte-surface proteins by enhanced chemiluminescence: a nonradioactive method for cell-surface protein analysis. Anal. Biochem.204, 220–226 (1992). ArticleCAS Google Scholar