viernes, 20 de agosto de 2010

Immunity - Development and Migration of Plasma Cells in the Mouse Lymph Node


Development and Migration of Plasma Cells in the Mouse Lymph Immunity, Volume 33, Issue 1, 118-127, 08 July 2010
Copyright 2010 Elsevier Inc. All rights reserved.
10.1016/j.immuni.2010.06.015

Referred to by: Plasma Cell Precursors: Long-Distance Tr...

Authors
David R. Fooksman, Tanja A. Schwickert, Gabriel D. Victora, Michael L. Dustin, Michel C. Nussenzweig, Dimitris SkokosSee AffiliationsHint: Rollover Authors and Affiliations Program in Molecular Pathogenesis and Department of Pathology, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, NY 10016, USA Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10021 USA Laboratory of Molecular Immunology, Howard Hughes Medical Institute, The Rockefeller University, New York, NY 10021 USA Regeneron Pharmaceuticals, Tarrytown, NY 10591-6707, USA Corresponding author These authors contributed equally to this work


Highlights
•Pre-PCs migrate in random directions with long free-path lengths without chemokines
•Pre-PCs migrate by a processive slide, which facilitates a long free-path length
•Pre-PC motility is inversely correlated with differentiation and is cell autonomous
•PC retention in the medullary cords is Ptx sensitive

Summary
In this study, we imaged the differentiation and migratory behavior of nascent plasma cells (PCs) in mouse lymph nodes by intravital microscopy. Pre-PCs exhibited a unique migration pattern characterized by long, linear paths that were randomly oriented. Although chemotaxis via Gαi coupled-receptors has been implicated in PC migration, treatment with Pertussis toxin (Ptx), which ablates these signals, did not prevent movement of pre-PCs while it arrested other lymphocytes. In vitro, pre-PCs displayed processive amoeboid locomotion on surfaces coated with integrin ligand, whereas fully differentiated PCs moved slowly or were arrested. Both PC arrest and differentiation occurred in the medullary cords. Ptx treatment before PC differentiation blocked their accumulation in the medullary cords but pre-PCs still differentiated in other lymph node regions. Taken together, we suggest pre-PCs undergo a persistent random walk to find the medullary cords, where localized chemokines help retain these cells until they undergo differentiation and arrest in situ.
10.1016/j.immuni.2010.06.015


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Immunity - Development and Migration of Plasma Cells in the Mouse Lymph Node




-1Germinal center dark and light zone organization is mediated by CXCR4 and CXCR5.
Allen, C.D., Ansel, K.M., Low, C., Lesley, R., Tamamura, H., Fujii, N., and Cyster, J.G. (2004)
Nat. Immunol.
5, 943952. View at PubMedView at PublisherImaging of germinal center selection events during affinity maturation.
Allen, C.D., Okada, T., Tang, H.L., and Cyster, J.G. (2007)
Science
315, 528531. View at PubMedView at PublisherCommitment of B lymphocytes to a plasma cell fate is associated with Blimp-1 expression in vivo.
Angelin-Duclos, C., Cattoretti, G., Lin, K.I., and Calame, K. (2000)
J. Immunol.
165, 54625471. View at PubMedStromal cell networks regulate lymphocyte entry, migration, and territoriality in lymph nodes.
Bajénoff, M., Egen, J.G., Koo, L.Y., Laugier, J.P., Brau, F., Glaichenhaus, N., and Germain, R.N. (2006)
Immunity
25, 9891001. View at PubMedView at PublisherAPRIL is critical for plasmablast survival in the bone marrow and poorly expressed by early-life bone marrow stromal cells.
Belnoue, E., Pihlgren, M., McGaha, T.L., Tougne, C., Rochat, A.F., Bossen, C., Schneider, P., Huard, B., Lambert, P.H., and Siegrist, C.A. (2008)
Blood
111, 27552764. View at PubMedView at PublisherRegulatory mechanisms that determine the development and function of plasma cells.
Calame, K.L., Lin, K.I., and Tunyaplin, C. (2003)
Annu. Rev. Immunol.
21, 205230. View at PubMedView at PublisherRandom walk models in biology.
Codling, E.A., Plank, M.J., and Benhamou, S. (2008)
J. R. Soc. Interface
5, 813834. View at PubMedView at PublisherSearch along persistent random walks.
Friedrich, B.M. (2008)
Phys. Biol.
5, 026007. View at PubMedView at PublisherThe subcellular localization of immunoglobulin in mouse plasma cells, as studied with immunoferritin cytochemistry on ultrathin frozen sections.
Geuze, H.J., and Slot, J.W. (1980)
Am. J. Anat.
158, 161169. View at PubMedView at PublisherA coordinated change in chemokine responsiveness guides plasma cell movements.
Hargreaves, D.C., Hyman, P.L., Lu, T.T., Ngo, V.N., Bidgol, A., Suzuki, G., Zou, Y.R., Littman, D.R., and Cyster, J.G. (2001)
J. Exp. Med.
194, 4556. View at PubMedView at PublisherChemotactic responsiveness toward ligands for CXCR3 and CXCR4 is regulated on plasma blasts during the time course of a memory immune response.
Hauser, A.E., Debes, G.F., Arce, S., Cassese, G., Hamann, A., Radbruch, A., and Manz, R.A. (2002)
J. Immunol.
169, 12771282. View at PubMedDistinct short-lived and long-lived antibody-producing cell populations.
Ho, F., Lortan, J.E., MacLennan, I.C., and Khan, M. (1986)
Eur. J. Immunol.
16, 12971301. View at PubMedView at PublisherRequirements for T lymphocyte migration in explanted lymph nodes.
Huang, J.H., Cárdenas-Navia, L.I., Caldwell, C.C., Plumb, T.J., Radu, C.G., Rocha, P.N., Wilder, T., Bromberg, J.S., Cronstein, B.N., and Sitkovsky, M., et al. (2007)
J. Immunol.
178, 77477755. View at PubMedMyosin-IIA and ICAM-1 regulate the interchange between two distinct modes of T cell migration.
Jacobelli, J., Bennett, F.C., Pandurangi, P., Tooley, A.J., and Krummel, M.F. (2009)
J. Immunol.
182, 20412050. View at PubMedView at PublisherPlasma cell S1P1 expression determines secondary lymphoid organ retention versus bone marrow tropism.
Kabashima, K., Haynes, N.M., Xu, Y., Nutt, S.L., Allende, M.L., Proia, R.L., and Cyster, J.G. (2006)
J. Exp. Med.
203, 26832690. View at PubMedView at PublisherPlasma cell ontogeny defined by quantitative changes in blimp-1 expression.
Kallies, A., Hasbold, J., Tarlinton, D.M., Dietrich, W., Corcoran, L.M., Hodgkin, P.D., and Nutt, S.L. (2004)
J. Exp. Med.
200, 967977. View at PubMedView at PublisherPertussis toxin and target eukaryotic cells: Binding, entry, and activation.
Kaslow, H.R., and Burns, D.L. (1992)
FASEB J.
6, 26842690. View at PubMedTwo-photon imaging of lymphocyte motility and antigen response in intact lymph node.
Miller, M.J., Wei, S.H., Parker, I., and Cahalan, M.D. (2002)
Science
296, 18691873. View at PubMedView at PublisherDendritic cells and monocyte/macrophages that create the IL-6/APRIL-rich lymph node microenvironments where plasmablasts mature.
Mohr, E., Serre, K., Manz, R.A., Cunningham, A.F., Khan, M., Hardie, D.L., Bird, R., and MacLennan, I.C. (2009)
J. Immunol.
182, 21132123. View at PubMedView at PublisherThymic microenvironments for T-cell repertoire formation.
Nitta, T., Murata, S., Ueno, T., Tanaka, K., and Takahama, Y. (2008)
Adv. Immunol.
99, 5994. View at PubMedView at PublisherB cell migration and interactions in the early phase of antibody responses.
Okada, T., and Cyster, J.G. (2006)
Curr. Opin. Immunol.
18, 278285. View at PubMedView at PublisherCutting edge: egress of newly generated plasma cells from peripheral lymph nodes depends on beta 2 integrin.
Pabst, O., Peters, T., Czeloth, N., Bernhardt, G., Scharffetter-Kochanek, K., and Förster, R. (2005)
J. Immunol.
174, 74927495. View at PubMedEBI2 mediates B cell segregation between the outer and centre follicle.
Pereira, J.P., Kelly, L.M., Xu, Y., and Cyster, J.G. (2009)
Nature
460, 11221126. View at PubMedCompetence and competition: The challenge of becoming a long-lived plasma cell.
Radbruch, A., Muehlinghaus, G., Luger, E.O., Inamine, A., Smith, K.G., Dörner, T., and Hiepe, F. (2006)
Nat. Rev. Immunol.
6, 741750. View at PubMedSphingosine 1-phosphate and its receptors: An autocrine and paracrine network.
Rosen, H., and Goetzl, E.J. (2005)
Nat. Rev. Immunol.
5, 560570. View at PubMedTranscriptional repressor Blimp-1 promotes CD8(+) T cell terminal differentiation and represses the acquisition of central memory T cell properties.
Rutishauser, R.L., Martins, G.A., Kalachikov, S., Chandele, A., Parish, I.A., Meffre, E., Jacob, J., Calame, K., and Kaech, S.M. (2009)
Immunity
31, 296308. View at PubMedView at PublisherFinding a way out: Lymphocyte egress from lymphoid organs.
Schwab, S.R., and Cyster, J.G. (2007)
Nat. Immunol.
8, 12951301. View at PubMedView at PublisherIn vivo imaging of germinal centres reveals a dynamic open structure.
Schwickert, T.A., Lindquist, R.L., Shakhar, G., Livshits, G., Skokos, D., Kosco-Vilbois, M.H., Dustin, M.L., and Nussenzweig, M.C. (2007)
Nature
446, 8387. View at PubMedView at PublisherBlimp-1 orchestrates plasma cell differentiation by extinguishing the mature B cell gene expression program.
Shaffer, A.L., Lin, K.I., Kuo, T.C., Yu, X., Hurt, E.M., Rosenwald, A., Giltnane, J.M., Yang, L., Zhao, H., Calame, K., et al. (2002)
Immunity
17, 5162. View at PubMedView at PublisherRole of antigen receptor affinity in T cell-independent antibody responses in vivo.
Shih, T.A., Roederer, M., and Nussenzweig, M.C. (2002)
Nat. Immunol.
3, 399406. View at PubMedView at PublisherThe phenotype and fate of the antibody-forming cells of the splenic foci.
Smith, K.G., Hewitson, T.D., Nossal, G.J., and Tarlinton, D.M. (1996)
Eur. J. Immunol.
26, 444448. View at PubMedView at PublisherSphingosine-1-phosphate: An enigmatic signalling lipid.
Spiegel, S., and Milstien, S. (2003)
Nat. Rev. Mol. Cell Biol.
4, 397407. View at PubMedView at PublisherIn situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. V. Affinity maturation develops in two stages of clonal selection.
Takahashi, Y., Dutta, P.R., Cerasoli, D.M., and Kelsoe, G. (1998)
J. Exp. Med.
187, 885895. View at PubMedView at PublisherPlasma cell differentiation and survival.
Tarlinton, D., Radbruch, A., Hiepe, F., and Dörner, T. (2008)
Curr. Opin. Immunol.
20, 162169. View at PubMedView at PublisherBlimp-1, a novel zinc finger-containing protein that can drive the maturation of B lymphocytes into immunoglobulin-secreting cells.
Turner, C.A., Mack, D.H., and Davis, M.M. (1994)
Cell
77, 297306. View at PubMedView at PublisherChanging responsiveness to chemokines allows medullary plasmablasts to leave lymph nodes.
Wehrli, N., Legler, D.F., Finke, D., Toellner, K.M., Loetscher, P., Baggiolini, M., MacLennan, I.C., and Acha-Orbea, H. (2001)
Eur. J. Immunol.
31, 609616. View at PubMedView at PublisherPosition effect variegation and imprinting of transgenes in lymphocytes.
Williams, A., Harker, N., Ktistaki, E., Veiga-Fernandes, H., Roderick, K., Tolaini, M., Norton, T., Williams, K., and Kioussis, D. (2008)
Nucleic Acids Res.
36, 23202329. View at PubMedView at PublisherDirected migration of positively selected thymocytes visualized in real time.
Witt, C.M., Raychaudhuri, S., Schaefer, B., Chakraborty, A.K., and Robey, E.A. (2005)
PLoS Biol.
3, e160. View at PubMedView at PublisherQuantification and regulation of cell migration.
Zygourakis, K. (1996)
Tissue Eng.
2, 116. View at PubMed

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