Ligand of scavenger receptor class A indirectly induces maturation of human blood dendritic cells via production of tumor necrosis factor-α

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Altschul, S. F., Gish, W., Miller, W., Myers, E. W., & Lipman, D. J. (1990) · Journal of Molecular Biology · doi:10.1006/jmbi.1990.9999 · Cited by 98,669 · see citing works

Dendritic cells and the control of immunity

Banchereau, J., & Steinman, R. M. (1998) · Nature · doi:10.1038/32588 · Cited by 14,244 · see citing works

Inhibition of glycogen synthase kinase-3 by insulin mediated by protein kinase B

Cross, D. A. E., Alessi, D. R., Cohen, P., Andjelkovich, M., & Hemmings, B. A. (1995) · Nature · doi:10.1038/378785a0 · Cited by 5,244 · see citing works

Efficient presentation of soluble antigen by cultured human dendritic cells is maintained by granulocyte/macrophage colony-stimulating factor plus interleukin 4 and downregulated by tumor necrosis factor alpha

Sallusto, F., & Lanzavecchia, A. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.179.4.1109 · Cited by 5,129 · see citing works

Toll-like receptor control of the adaptive immune responses

Iwasaki, A., & Medzhitov, R. M. (2004) · Nature Immunology · doi:10.1038/ni1112 · Cited by 4,166 · see citing works

GM-CSF and TNF-α cooperate in the generation of dendritic Langerhans cells

Caux, C., Dezutter‐Dambuyant, C., Schmitt, D., & Banchereau, J. (1992) · Nature · doi:10.1038/360258a0 · Cited by 1,551 · see citing works

BDCA-2, BDCA-3, and BDCA-4: Three Markers for Distinct Subsets of Dendritic Cells in Human Peripheral Blood

Dzionek, A., Fuchs, A., Schmidt, P., Cremer, S., Zysk, M., Miltenyi, S., Buck, D., & Schmitz, J. (2000) · Journal of Immunology · doi:10.4049/jimmunol.165.11.6037 · Cited by 1,433 · see citing works

Origin, maturation and antigen presenting function of dendritic cells

Cella, M., Sallusto, F., & Lanzavecchia, A. (1997) · Current Opinion in Immunology · doi:10.1016/s0952-7915(97)80153-7 · Cited by 1,339 · see citing works

Activation of human dendritic cells through CD40 cross-linking.

Caux, C., Massacrier, C., Vanbervliet, B., Dubois, B., van Kooten, C., Durand, I., & Banchereau, J. (1994) · The Journal of Experimental Medicine · doi:10.1084/jem.180.4.1263 · Cited by 1,317 · see citing works

Steady-state and inflammatory dendritic-cell development

Shortman, K., & Naik, S. H. (2006) · Nature reviews. Immunology · doi:10.1038/nri1996 · Cited by 1,180 · see citing works

STRUCTURES AND FUNCTIONS OF MULTILIGAND LIPOPROTEIN RECEPTORS: Macrophage Scavenger Receptors and LDL Receptor-Related Protein (LRP)

Krieger, M., & Krieger, J. (1994) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.63.070194.003125 · Cited by 1,160 · see citing works

Pattern Recognition Receptors

Gordon, S. (2002) · Cell · doi:10.1016/s0092-8674(02)01201-1 · Cited by 1,153 · see citing works

CD14+ blood monocytes can differentiate into functionally mature CD83+ dendritic cells.

Zhou, L., & Tedder, T. F. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.6.2588 · Cited by 1,090 · see citing works

Toll-like receptor–mediated cytokine production is differentially regulated by glycogen synthase kinase 3

Martin, M., Rehani, K., Jope, R. S., & Michalek, S. M. (2005) · Nature Immunology · doi:10.1038/ni1221 · Cited by 1,080 · see citing works

A comparative study of the anti-inflammatory, anticoagulant, antiangiogenic, and antiadhesive activities of nine different fucoidans from brown seaweeds

Cumashi, A., Ushakova, N. A., Preobrazhenskaya, M. E., D'Incecco, A., Piccoli, A., Totani, L., Tinari, N., Morozevich, G. E., Berman, A. E., Bilan, M. I., et al. (2007) · Glycobiology · doi:10.1093/glycob/cwm014 · Cited by 1,026 · see citing works

Sulfated fucans, fresh perspectives: Structures, functions, and biological properties of sulfated fucans and an overview of enzymes active toward this class of polysaccharide

Berteau, O. (2003) · Glycobiology · doi:10.1093/glycob/cwg058 · Cited by 769 · see citing works

Characterization of human blood dendritic cell subsets

MacDonald, K. P. A., Munster, D. J., Clark, G. J., Dzionek, A., Schmitz, J., & Hart, D. N. J. (2002) · Blood · doi:10.1182/blood-2001-11-0097 · Cited by 755 · see citing works

The Linkage of Innate to Adaptive Immunity via Maturing Dendritic Cells In Vivo Requires CD40 Ligation in Addition to Antigen Presentation and CD80/86 Costimulation

Fujii, S., Liu, K., Smith, C., Bonito, A., & Steinman, R. (2004) · Journal of Experimental Medicine · doi:10.1084/jem.20040317 · Cited by 647 · see citing works

CpG DNA: A potent signal for growth, activation, and maturation of human dendritic cells

Hartmann, G., Weiner, G. J., & KRIEG, A. M. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.16.9305 · Cited by 617 · see citing works

Human blood contains two subsets of dendritic cells, one immunologically mature and the other immature.

O’Doherty, U., Peng, M., Gezelter, S., Swiggard, W. J., Betjes, M. G. H., Bhardwaj, N., & Steinman, R. M. (1994) · PubMed Central · Cited by 601 · see citing works

Intrasplenic steady-state dendritic cell precursors that are distinct from monocytes

Naik, S. H., Metcalf, D., van Nieuwenhuijze, A. E. M., Wicks, I. P., Wu, L., O’Keeffe, M. A., & Shortman, K. (2006) · Nature Immunology · doi:10.1038/ni1340 · Cited by 598 · see citing works

Repetitive Injections of Dendritic Cells Matured with Tumor Necrosis Factor α Induce Antigen-specific Protection of Mice from Autoimmunity

Menges, M., Rößner, S., Voigtländer, C., Schindler, H., Kukutsch, N. A., Bogdan, C., Erb, K. J., Schuler, G., & Lutz, M. B. (2001) · The Journal of Experimental Medicine · doi:10.1084/jem.20011341 · Cited by 556 · see citing works

Reactivity of Langerhans cells with hybridoma antibody.

Fithian, E., Kung, P. C., Goldstein, G., Rubenfeld, M. R., Fenoglio, C. M., & Edelson, R. (1981) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.78.4.2541 · Cited by 555 · see citing works

Recognition and plasma clearance of endotoxin by scavenger receptors

Hampton, R. Y., Golenbock, D. T., Penman, M., Krieger, M., & Raetz, C. R. H. (1991) · Nature · doi:10.1038/352342a0 · Cited by 524 · see citing works

Flt3-Ligand and Granulocyte Colony-Stimulating Factor Mobilize Distinct Human Dendritic Cell Subsets In Vivo

Pulendran, B., Banchereau, J., Burkeholder, S. B., Kraus, E., Guinet, E., Chalouni, C. M., Caron, D. A., Maliszewski, C. R., Davoust, J. M., Fay, J. W., et al. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.165.1.566 · Cited by 407 · see citing works

A Critical Role for p38 Mitogen-Activated Protein Kinase in the Maturation of Human Blood-Derived Dendritic Cells Induced by Lipopolysaccharide, TNF-α, and Contact Sensitizers

Arrighi, J.-F., Rebsamen, M. C., Rousset, F., et al. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.6.3837 · Cited by 403 · see citing works

Selective Suppression of Interleukin-12 Induction after Macrophage Receptor Ligation

Sutterwala, F. S., Noel, G. J., Clynes, R., & Mosser, D. M. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.185.11.1977 · Cited by 351 · see citing works

Toll-like receptors and dendritic cells: for whom the bug tolls

Sousa, C. R. E. (2004) · Seminars in Immunology · doi:10.1016/j.smim.2003.10.004 · Cited by 341 · see citing works

Prostaglandin E2 and Tumor Necrosis Factor α Cooperate to Activate Human Dendritic Cells: Synergistic Activation of Interleukin 12 Production

Rieser, C., Böck, G., Klocker, H., Bartsch, G. H., & Thurnher, M. (1997) · The Journal of Experimental Medicine · doi:10.1084/jem.186.9.1603 · Cited by 274 · see citing works

Mammalian target of rapamycin and glycogen synthase kinase 3 differentially regulate lipopolysaccharide-induced interleukin-12 production in dendritic cells

Ohtani, M., Nagai, S., Kondo, S., Mizuno, S., Nakamura, K., Tanabe, M., Takeuchi, T., Matsuda, S., & Koyasu, S. (2008) · Blood · doi:10.1182/blood-2008-02-137430 · Cited by 265 · see citing works

Myeloid blood CD11c+ dendritic cells and monocyte-derived dendritic cells differ in their ability to stimulate T lymphocytes

Osugi, Y., Vučković, S., & Hart, D. N. J. (2002) · Blood · doi:10.1182/blood.v100.8.2858 · Cited by 215 · see citing works

A Role for Class A Scavenger Receptor in Dendritic Cell Nibbling from Live Cells

Harshyne, L. A., Zimmer, M. I., Watkins, S. C., et al. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.5.2302 · Cited by 189 · see citing works

Ligands of Macrophage Scavenger Receptor Induce Cytokine Expression via Differential Modulation of Protein Kinase Signaling Pathways

Hsu, H., Chiu, S.-L., Wen, M., Chen, K.-Y., & Hua, K. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m011117200 · Cited by 169 · see citing works

Advanced Glycosylation End Products Might Promote Atherosclerosis Through Inducing the Immune Maturation of Dendritic Cells

Ge, J., Jia, Q., Liang, C., et al. (2005) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000181744.58265.63 · Cited by 129 · see citing works

Oxidized Low-Density Lipoprotein Promotes Mature Dendritic Cell Transition from Differentiating Monocyte

Perrin‐Cocon, L., Coutant, F., Agaugué, S., Deforges, S., André, P., & Lotteau, V. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.7.3785 · Cited by 129 · see citing works

Structures and Functions of Multiligand and Lipoprotein Receptors

Krieger, M. (1994) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.63.1.601 · Cited by 118 · see citing works

GSK-3 mediates differentiation and activation of proinflammatory dendritic cells

Rodionova, E., Conzelmann, M., Maraskovsky, E., Heß, M., Kirsch, M., Giese, T., Ho, A. D., Zöller, M., Dreger, P., & Luft, T. (2006) · Blood · doi:10.1182/blood-2006-06-028951 · Cited by 108 · see citing works

Ligand Binding to Macrophage Scavenger Receptor-A Induces Urokinase-type Plasminogen Activator Expression by a Protein Kinase-dependent Signaling Pathway

Hsu, H., Hajjar, D. P., Khan, K. M. F., & Falcone, D. J. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.2.1240 · Cited by 99 · see citing works

Whence Interferon? Variety in the Production of Interferon in Response to Viral Infection

Levy, D. E. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20020075 · Cited by 92 · see citing works

The Many Roles of the Class A Macrophage Scavenger Receptor

Platt, N., Haworth, R., Darley, L., & Gordon, S. (2002) · International review of cytology · doi:10.1016/s0074-7696(01)12002-4 · Cited by 80 · see citing works

Scavenger Receptor-A Negatively Regulates Antitumor Immunity

Wang, X., Facciponte, J. G., Chen, X., et al. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-3138 · Cited by 75 · see citing works

Expression of the class A macrophage scavenger receptor on specific subpopulations of murine dendritic cells limits their endotoxin response

Becker, M. O., Cotena, A., Gordon, S., & Platt, N. (2006) · European Journal of Immunology · doi:10.1002/eji.200535660 · Cited by 67 · see citing works

Inhibition of complement activation by water-soluble polysaccharides of some far-eastern brown seaweeds

Николаевна, З. Т., Шевченко, Н. М., Nazarova, I. V., Scobun, A. S., Lukyanov, P. A., & Elyakova, L. A. (2000) · Comparative Biochemistry and Physiology Part C Pharmacology Toxicology and Endocrinology · doi:10.1016/s0742-8413(00)00114-6 · Cited by 41 · see citing works

Scavenger receptor-A functions in phagocytosis of E. coli by bone marrow dendritic cells

Amiel, E., Nicholson-Dykstra, S., Walters, J. J., et al. (2007) · Experimental Cell Research · doi:10.1016/j.yexcr.2007.02.011 · Cited by 33 · see citing works

Differential maturation of murine bone-marrow derived dendritic cells with lipopolysaccharide and tumor necrosis factor-α

Efron, P. A., Tsujimoto, H., Bahjat, F. R., Ungaro, R. F., Debernardis, J., Tannahill, C. L., Baker, H. V., Edwards, C. K., & Moldawer, L. L. (2005) · Journal of Endotoxin Research · doi:10.1179/096805105x46583 · Cited by 24 · see citing works

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(1999) · doi:10.1002/(sici)1521-4141(199909)29:09

Anticancer and Cancer Preventive Properties of Marine Polysaccharides: Some Results and Prospects

Fedorov, S., Ermakova, S., Zvyagintseva, T., & Stonik, V. (2013) · Marine Drugs · doi:10.3390/md11124876 · Cited by 189 · see citing works

Fucoidan Can Function as an Adjuvant In Vivo to Enhance Dendritic Cell Maturation and Function and Promote Antigen-Specific T Cell Immune Responses

Jin, J.-O., Zhang, W., Du, J.-Y., Wong, K.-W., Oda, T., & Yu, Q. (2014) · PLoS ONE · doi:10.1371/journal.pone.0099396 · Cited by 160 · see citing works

Fucoidans from Brown Alga Fucus evanescens: Structure and Biological Activity

Menshova, R. V., Shevchenko, N. M., Imbs, T. I., Zvyagintseva, T. N., Malyarenko, O. S., Zaporoshets, T. S., Besednova, N. N., & Ermakova, S. P. (2016) · Frontiers in Marine Science · doi:10.3389/fmars.2016.00129 · Cited by 85 · see citing works

FUCOIDAN FROM BROWN SEAWEED AND ITS BIOACTIVITY

Sinurat, E., & Marraskuranto, E. (2013) · SQUALEN Bulletin of Marine and Fisheries Postharvest and Biotechnology · doi:10.15578/squalen.v7i3.8 · Cited by 16 · see citing works

In-vitro anticoagulant activity of fucoidan derivatives from brown seaweed Laminaria japonica

王晶, 张全斌, 张忠山, et al. (2011) · Acta Scientiarum Naturalium Universitatis Sunyatseni

Evaluation of Fucoidan Bioactivity as Anti Gastric Ulcers in Mice

Sinurat, E., & Rosmawaty, P. D. (2015) · Procedia Environmental Sciences · doi:10.1016/j.proenv.2015.01.058 · Cited by 9 · see citing works

Induction of hepatocyte growth factor by fucoidan and fucoidan-derived oligosaccharides

Fukuta, K., & Nakamura, T. (2008) · Journal of Pharmacy and Pharmacology · doi:10.1211/jpp.60.4.0013 · Cited by 21 · see citing works

Physicochemical characterization of Sargassum fusiforme fucoidan fractions and their antagonistic effect against P-selectin-mediated cell adhesion

Wu, S., Zhang, X., Liu, J., et al. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.03.218 · Cited by 47 · see citing works