Agranulocitos: linfocitos y monocitos. R: Comprenden aprox. Existen tres tipos: T, B y NK. R : Contiene una cantidad variable de tejido adiposo organizado en lobulillos separados por.
R: Epitelio estratificad plano. R: Tipo celular p redominante de la epidermis. R: Producen la melanina y la distribuyen entre lo s queratinocitos. R: Conjunto de cr estas y surcos qu e se distribuyen en la piel gruesa. R: Al momento de que los melanocitos producen melanina, esta sea secretada de manera. R: Los bordes y las palmas de las manos, los borden y las plantas de l os pies, el borde libre de. Describe cada uno:.
R: La base del bulb o esta invaginada por un ovillejo de tejido conjuntivo laxo vascularizado,. R: Mucosa masticatoria, mucosa de revestimiento y mucosa especializada. R: Epitelio estratificado plano queratinizado y en algunas zonas paraquer atinizado. R: Labios, mejillas, la superficie mucosa alveolar, el piso de la boca, la superficie ventral de la.
R: Estratificado plano no queratinizado, pero en algunos sitios puede estar paraqueratinizado. R: Filiformes, fungiformes, calciformes o circunvaladas y foliadas.
R: Esmalte, dentina y cemento. Es una capa delgada de material similar al hueso. Witmer, M. Dendritic cells are the principal stimulators of the primary mixed leukocyte reaction in mice. Lopez, L.
Amorim, P. Gane, A. Cristoph, D. Bardinet, A. Abina, et al. J Immunol Methods, , pp. Luft, K. Pang, E. Thomas, C. Bradley, H. Savoia, J. Trapani, et al. Exp Hematol, 26 , pp. Berger, B. Feuerstein, E. Strasser, U.
Hirsch, D. Schreiner, G. Schuler, et al. Large-scale generation of mature monocyte-derived dendritic cells for clinical application in cell factories. Felzmann, V. Witt, D. Wimmer, G. Ressmann, D. Wagner, P. Paul, et al. Monocyte enrichment from leukapharesis products for the generation of DCs by plastic adherence, or by positive or negative selection.
Cytotherapy, 5 , pp. Dzionek, A. Fuchs, P. Schmidt, S. Cremer, M. Zysk, S. Miltenyi, et al. J Immunol, , pp.
Niess, S. Brand, X. Gu, L. Landsman, S. Jung, B. McCormick, et al. CX3CR1-mediated dendritic cell access to the intestinal lumen and bacterial clearance. Science, , pp. Rescigno, M.
Urbano, B. Valzasina, M. Francolini, G. Rotta, R. Bonasio, et al. Dendritic cells express tight junction proteins and penetrate gut epithelial monolayers to sample bacteria. Nat Immunol, 2 , pp. Dendritic cells: unique leukocyte populations which control the primary immune response. Blood, 90 , pp. Hart, T. Adhesion molecules in tonsil DC-T cell interactions.
Adv Exp Med Biol, , pp. Banchereau, F. Bazan, D. Blanchard, F. Galizzi, C. Annu Rev Immunol, 12 , pp. Fagnoni, M. Takamizawa, W. Godfrey, A. Rivas, M. Azuma, K. Okumura, et al. Immunology, 85 , pp. Takamizawa, A. Rivas, F. Fagnoni, C. Benike, J. Kosek, H. Hyakawa, et al. McLellan, G. Starling, L. Williams, B. Hock, D. Activation of human peripheral blood dendritic cells induces the CD86 co-stimulatory molecule. Eur J Immunol, 25 , pp. Human follicular dendritic cells: function, origin and development.
Semin Immunol, 14 , pp. Pulendran, J. Banchereau, S. Burkeholder, E. Kraus, E. Guinet, C. Chalouni, et al. Flt3-ligand and granulocyte colony-stimulating factor mobilize distinct human dendritic cell subsets in vivo. MacDonald, D. Munster, G. Clark, A. Dzionek, J. Schmitz, D. Characterization of human blood dendritic cell subsets.
Blood, , pp. Szabolcs, K. Park, M. Reese, L. Marti, G. Broadwater, J. Absolute values of dendritic cell subsets in bone marrow, cord blood, and peripheral blood enumerated by a novel method. Stem Cells, 21 , pp. Palucka, N. Taquet, F. Sanchez-Chapuis, J. Dendritic cells as the terminal stage of monocyte differentiation.
Oehler, O. Majdic, W. Pickl, J. Stockl, E. Riedl, J. Drach, et al. Neitrophil granulocyte-committed cells can be driven to acquire dendritic cells characteristics. Sylva-Steenland, J. Bos, M. Kapsenberg, E. De Jong, M. Klechevsky, M. Liu, R. Morita, R. Banchereau, L. Thompson-Snipes, A. Palucka, et al. Understanding human myeloid dendritic cell subsets for the rational design of novel vaccines.
Hum Immunol, 70 , pp. Flacher, M. Bouschbacher, E. Massacrier, V. Sisirak, O. Berthier-Vergnes, et al. Human Langerhans cells express a specific TLR profile and differentially respond to viruses and Gram-positive bacteria. Klechevsky, R. Morita, M. Liu, Y. Cao, S. Coquery, L. Thompson-Snipes, et al. Immunity, 29 , pp. Schmitt, R. Morita, L. Bourdery, S. Bentebibel, S. Zurawski, J.
Banchereau, et al. Human dendritic cells induce the differentiation of interleukinproducing T follicular helper-like cells through interleukin Immunity, 31 , pp. Oh, L. Perera, D. Burke, T. Waldmann, J. Kadowaki, S. Ho, S. Antonenko, R. Malefyt, R. Kastelein, F. Bazan, et al. Subsets of human dendritic cell precursors express different toll-like receptors and respond to different microbial antigens.
Dzionek, Y. Sohma, J. Nagafune, M. Cella, M. Colonna, F. Facchetti, et al. Cella, D. Jarrossay, F. Facchetti, O. Alebardi, H. Nakajima, A. Lanzavecchia, et al. Plasmacytoid monocytes migrate to inflamed lymph nodes and produce large amounts of type I interferon.
Nat Med, 5 , pp. Grouard, M. Rissoan, L. Filgueira, I. Durand, J. Banchereau, Y. The enigmatic plasmacytoid T cells develop into dendritic cells with interleukin IL -3 and CDligand. Krug, S. Rothenfusser, V. Hornung, B. Blackwell, Z. Ballas, et al. Eur J Immunol, 31 , pp. CO;2-U Medline. Fonteneau, M. Gilliet, M. Larsson, I. Dasilva, C. Liu, et al. Ito, M. Yang, Y. Wang, R. Lande, J. Gregorio, O. Perng, et al. Plasmacytoid dendritic cells prime ILproducing T regulatory cells by inducible costimulator ligand.
Gilliet, Y. Matsui, J. Connolly, M. Michnevitz, D. Chaussabel, C. Yu, C. Glaser, et al. CD2 distinguishes two subsets of human plasmacytoid dendritic cells with distinct phenotype and functions.
Arpinati, C. Green, S. Heimfeld, J. Heuser, C. Granulocyte-colony stimulating factor mobilizes T helper 2-inducing dendritic cells. Blood, 95 , pp. Shortman, Y. Nat Rev Immunol, 2 , pp. Robert, R. Fuhlbrigge, J. Kieffer, S. Ayehunie, R. Hynes, G. Cheng, et al. Interaction of dendritic cells with skin endothelium: A new perspective on immunosurveillance. Greaves, W. Wang, D. Dairaghi, M.
Dieu, B. Saint-Vis, K. Franz-Bacon, et al. CCR6, a CC chemokine receptor that interacts with macrophage inflammatory protein 3alpha and is highly expressed in human dendritic cells. Sozzani, P. Allavena, G. Luini, G. Bianchi, M. Kataura, et al. Differential regulation of chemokine receptors during dendritic cell maturation: a model for their trafficking properties.
Rafiq, A. Bergtold, R. Immune complex-mediated antigen presentation induces tumor immunity. J Clin Invest, , pp. Albert, S.
Pearce, L. Francisco, B. Sauter, P. Roy, R. Silverstein, et al. Immature dendritic cells phagocytose apoptotic cells via alphavbeta5 and CD36, and cross-present antigens to cytotoxic T lymphocytes.
Bonifaz, D. Bonnyay, K. Mahnke, M. Rivera, M. Nussenzweig, R. Peiser, S. Mukhopadhyay, S. Curr Opin Immunol, 14 , pp. Ackerman, P. Cellular mechanisms governing cross-presentation of exogenous antigens. Nat Immunol, 5 , pp. Joyce, L. Van Kaer. CD1-restricted antigen presentation: an oily matter.
Curr Opin Immunol, 15 , pp. Briere, C. Caux, J. Davoust, S. Lebecque, Y. Annu Rev Immunol, 18 , pp. Rossi, J. Human dendritic cells: potent antigen-presenting cells at the crossroads of innate and adaptative immunity. The danger model: a renewed sense of self.
Skoberne, A.
0コメント