MAdCAM-1 Dependent Colonization of Developing Lymph Nodes Involves a Unique Subset of CD4+CD3- Hematolymphoid Cells

References

• Adachi S., Yoshida H., Kataoka H., Nishikawa S.-I. Three distinctive steps in Peyer's patch formation of murine embryo. Int. Immunol. 1997; 9: 507–514
   PubMed Web of Science ®Google Scholar
• Alimzhanov M. B., Kuprash D. V., Kosco-Vilbois M. H., Luz A., Turetskaya R. L., Tarakhovsky A., Rajewsky K., Nedospasov S. A., Pfeffer K. Abnormal development of secondary lymphoid tissue in lymphotoxin β-deficient nice. Proc. Natl. Acad. Sci. USA 1997; 94: 9302–9307
   PubMed Web of Science ®Google Scholar
• Banks T. A., Rouse B. T., Kerley M. K., Blair P. J., Godfrey V. L., Kuklin N. A., Bouley D. M., Thomas J., Kanangat S., Mucenski M. L. Lymphotoxin-α-deficient mice. J. Immunol. 1995; 155: 1685–1693
   PubMed Web of Science ®Google Scholar
• Berg E. L., Robinson M. K., Warnock R. A., Butcher E. C. The human peripheral lymph node vascular addressin is a ligand for LECAM-1, the peripheral lymph node homing receptor. J. Cell Biol. 1991; 114: 343–349
   PubMed Web of Science ®Google Scholar
• Berlin C., Bargatze R. F., Campbell J. J., Andrian U. H.v., Szabo M. C., Hasslen S. R., Nelson R. D., Berg E. L., Erlandsen S. L., Butcher E. C. α4 integrins mediate lymphocyte attachment and rolling under physiologic flow. Cell. 1995; 80: 413–422
   PubMed Web of Science ®Google Scholar
• Berlin C., Berg E. L., Briskin M. J., Andrew D. P., Kilshaw P. J., Holzmann B., Weissman I. L., Hamann A., Butcher E. C. Alpha 4 beta 7 integrin mediates lymphocyte binding to the mucosal vascular addressin MAdCAM-1. Cell. 1993; 74: 185–195
   PubMed Web of Science ®Google Scholar
• Briskin M. J., McEnvoy L. M., Butcher E. C. MAdCAM-1 has homology to immunoglobulin and mucinlike adhesion receptors and to IgA1. Nature 1993; 363: 461–464
   PubMed Web of Science ®Google Scholar
• Burkly L., Hession C., Ogata L., Relly C., Marconi L. A., Olson D., Tizard R., Cate R., Lo D. Expression of relB is required for the development of thymic medulla and dendritic cells. Nature 1995; 373: 531–536
   PubMed Web of Science ®Google Scholar
• Butcher E. C. Leukocyte-endothelial cell recognition: three (or more) steps to specificity and diversity. Cell. 1991; 67: 1033–1036
   PubMed Web of Science ®Google Scholar
• Cao X., Shores E. W., Hu-Li J., Anver M. R., Kelsall B. L., Russell S. M., Drago J., Noguchi M., Grinberg A., Bloom E. T., Paul W. E., Katz S. I., Love P. E., Leonard W. J. Defective lymphoid development in mice lacking expression of the common cytokine receptor γ chain. Immunity. 1995; 2: 223–238
   PubMed Web of Science ®Google Scholar
• Eugster H., Muller M., Karrer U., Car B. D., Schnyder B., Eng V. M., Woerly G., Hir M. L., Padova F. d., Aguet M., Zlnkernagel R., Bluethmann H., Ryffel B. Multiple immune abnormalities in tumor necrosis factor and lymphotoxin-a double-deficient mice. Int. Immunol. 1996; 8: 23–26
   PubMed Web of Science ®Google Scholar
• Förster R., Mattis A. E., Kremmer E., Wolf E., Brem G., Lipp M. A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen. Cell. 1996; 87: 1037–1047
   PubMed Web of Science ®Google Scholar
• Freeden-Jeffry U. v., Vieira P., Lucian L. A., McNeil T., Burdach S. E.G., Murray R. Lymphopenia in Interleukin (IL)-7 gene-deleted mice identifies IL-7 as a nonredunadant cytokine. J. Exp. Med. 1995; 181: 1519–1526
   PubMed Web of Science ®Google Scholar
• Gallatin W. M., Weissman I. L., Butcher E. C. A cell-surface molecule involved in organ-specific homing of lymphocytes. Nature 1983; 304: 30–34
   PubMed Web of Science ®Google Scholar
• Galy A., Travis M., Cen D., Chen B. Human T, B, natural killer, and dendritic cells arise from a common bone marrow progenitor cell subset. Immunity. 1995; 3: 459–473
   PubMed Web of Science ®Google Scholar
• Georgopoulos K., Bigby M., Wang J.-H., Molnar A., Wu P., Winandy S. The Ikaros gene is required for the development of all lymphoid lineages. Cell. 1994; 79: 143–156
   PubMed Web of Science ®Google Scholar
• Gowans J. L., Knight E. J. The route of re-circulation of lymphocytes in the rat. Proc. Roy. Soc. Biol. 1964; 159: 257–282
   PubMed Web of Science ®Google Scholar
• Grouard G., Durand I., Filgueira L., Banchereau J., Liu Y. J. Dendritic cells capable of stimulating T cells in germinal centres. Nature 1996; 384: 364–367
   PubMed Web of Science ®Google Scholar
• Hamann A., Andrew D. P., Jablonski-Westrich D., Holzmann B., Butcher E. C. Role of α4-integrins in lymphocyte homing to mucosal tissues in vivo. J. Immunol. 1994; 152: 3282–3293
   PubMed Web of Science ®Google Scholar
• Holzmann B., McIntyre B. W., Weissman I. L. Identification of a murine Peyer's patch-specific lymphocyte homing receptor as an integrin with a chain homologous to human VLA-4. Cell. 1989; 56: 37–46
   PubMed Web of Science ®Google Scholar
• Holzmann B., Weissman I. L. Peyer's patch-specific lymphocyte horning receptors consist of a VLA-4-like α chain associated with either of two integrin beta chains, one of which is novel. EMBO J. 1989; 8: 1735–1741
   PubMed Web of Science ®Google Scholar
• Hu M. C.-T., Crowe D. T., Weissman I. L., Holzmann B. Cloning and expression of mouse integrin βp (β7): a functional role in Peyer's patch-specific homing. Proc. Natl. Acad. Sci. USA 1992; 89: 8254–8258
   PubMed Web of Science ®Google Scholar
• Humphrey J. H., Grennan D., Sundaram V. The origin of follicular dendritic cells in the mouse and the mechanism of trapping of immune complexes on them. Eur. J. Immunol. 1984; 14: 859–864
   PubMed Web of Science ®Google Scholar
• Kaipainen A., Korhonen J., Mustonen T., Hinsbergh V. W.M.v., Fang G.-H., Dumont D., Breitman M., Alitalo K. Expression of the fms-like tyrosine kinase 4 gene becomes restricted to lymphatic endothelium during development. Proc. Natl. Acad. Sci. USA 1995; 92: 3566–3570
   PubMed Web of Science ®Google Scholar
• Kelly K. A., Scollay R. Seeding of neonatal lymph nodes by T cells and identification of a novel population of CD3–CD4+ cells. Eur. J. Immunol. 1992; 22: 329–334
   PubMed Web of Science ®Google Scholar
• Koni P. A., Sacca R., Lawton P., Browning J. L., Ruddle N. H., Flavell R. A. Distinct roles in lymphoid organogenesis for lymphotoxins α and β revealed in lymphotoxin β-deficient mice. Immunity. 1997; 6: 491–500
   PubMed Web of Science ®Google Scholar
• Kraal G., Mebius R. E. High endothelial venules: lymphocyte traffic control and controlled traffic. Adv. hnmunol. 1997; 65: 347–395
   PubMed Web of Science ®Google Scholar
• Leene W. Origin and fate of lymphoid cells in the developing palatine tonsil of the rabbit. Z Zellforschung. 1971; 116: 502–522
   PubMedGoogle Scholar
• Lo D., Quill H., Burkly L, Scott B., Palmiter R. D., Brinster R. L. A recessive defect in lymphocyte or granulocyte function caused by an integrated transgene. Am. J. Pathol. 1992; 141: 1237–1246
   PubMed Web of Science ®Google Scholar
• Mebius R. E., Rennert P., Weissman I. L. Developing lymph nodes selectively collect CD4+CD3–LTb+ cells that can differentiate to dendritic APC, NK cells, and follicular cells, but not T- or B-cells. Immunity. 1997; 7: 494–504
   Web of Science ®Google Scholar
• Mebius R. E., Streeter P. R., Michie S., Butcher E. C., Weissman I. L. A developmental switch in lymphocyte homing receptor and endothelial vascular addressin expression regulates lymphocyte homing and permits CD4+CD3-cells to colonize lymph nodes. Proc. Natl. Acad. Sci. USA 1996; 93: 11019–11024
   PubMed Web of Science ®Google Scholar
• Medvinsky A., Dzierzak E. Definitive hematopoiesis is autonomously initiated by the AGM region. Cell. 1996; 86: 897–906
   PubMed Web of Science ®Google Scholar
• Medvinsky A. L., Samoylina N. L., Muller A. M., Dzierzak E. A. An early pre-liver intra-embryonic source of CFU-S in the developing mouse. Nature 1993; 364: 64–67
   PubMed Web of Science ®Google Scholar
• Müller A. M., Medvinsky A. L., Strouboulis J., Grosveld F., Dzierzak E. Development of hematopoietic stem cell activity in the mouse embryo. Immunity. 1994; 1: 291–301
   PubMed Web of Science ®Google Scholar
• Rennert P. D., Browning J. L., Mebius R., Mackay F., Hochman P. S. Surface lymphotoxin alpha/beta complex is required for the development of peripheral lymphoid organs. J. Exp. Med. 1996; 184: 1999–2006
   PubMed Web of Science ®Google Scholar
• Sabin F. R. On the origin of the lymphatic system from the veins, and the development of the lymph hearts and thoracic duct in the pig. Am. J. Anat. 1902; 1: 367–389
   Google Scholar
• Sabin F. R. On the development of the superficial lymphatics in the skin of the pig. Am. J. Anat. 1904; 3: 183–195
   Google Scholar
• Sabin F. R. Further evidence on the origin of the lymphatic endothelium from the endothelium of the blood vascular system. Anal. Rec. 1908; 2: 46–55
   Google Scholar
• Schriever F., Freeman G., Nadler L. M. Follicular dendritic cells contain a unique gene repertoire demonstrated by a single-cell polymerase chain reaction. Blood. 1991; 77: 787–791
   PubMed Web of Science ®Google Scholar
• Shimizu Y., Newman W., Tanaka Y., Shaw S. Lymphocyte interactions with endothelial cells. Inununol. Today. 1992; 13: 106–110
   PubMed Web of Science ®Google Scholar
• Spencer J., MacDonald T. T., Finn T., Isaacson P. G. The development of gut associated lymphoid tissue in the terminal ileum of fetal human intestine. Clin. Exp. Immunol. 1986; 64: 536–543
   PubMed Web of Science ®Google Scholar
• Springer T. A. Traffic signals for lymphocyte recirculation and leukocyte emigration: the multistep paradigm. Cell. 1994; 76: 301–314
   PubMed Web of Science ®Google Scholar
• Streeter P. R., Berg E. L., Rouse B. T.N., Bargatze R. F., Butcher E. C. A tissue-specific endothelial cell molecule involved in lymphocyte homing. Nature 1988; 331: 41–46
   PubMed Web of Science ®Google Scholar
• Streeter P. R., Rouse B. T.N., Butcher E. C. Immunohistologic and functional characterization of a vascular addressin involved in lymphocyte homing into peripheral lymph nodes. J. Cell Biol. 1988–96; 107: 1853–1862
   PubMed Web of Science ®Google Scholar
• Szakal A. K., Kapasi Z. F., Haley S. T., Tew. Multiple lines of evidence favoring a bone marrow derivation of follicular dendritic cells (FDCs). Adv. Exp. Med Biol. 1995; 378: 267–272
   PubMedGoogle Scholar
• Togni P. D., Goellner J., Ruddle N. H., Streeter P. R., Fick A., Mariathasan S., Smith S. C., Carlson R., Shornick L. P., Strauss-Schoenberger J., Russell J. H., Karr R., Chaplin D. D. Abnormal development of peripheral lymphoid organs in mice deficient in lymphotoxin. Science 1994; 264: 703–707
   PubMed Web of Science ®Google Scholar
• Wang J.-H., Nichogiannopoulou A., Wu L., Sun L., Sharpe A. H., Bigby M., Georgopoulous K. Selective defects in the development of the fetal and adult lymphoid system in mice with an Ikaros null mutation. Immunity. 1996; 5: 537–549
   PubMed Web of Science ®Google Scholar
• Weih F., Carrasco D., Durham S. K., Barton D. S., Rizzo C. A., Ryseck R., Lira S. A., Bravo R. Multiorgan inflammation and hematopoietic abnormalities in mice with a targeted disruption of RelB, a member of the NF-kB/Rel family. Cell. 1995; 80: 331–340
   PubMed Web of Science ®Google Scholar
• Wu L., Antica M., Johnson G. R., Scollay R., Shortman K. Developmental potential of the earliest precursor cells from the adult mouse thymus. J. Exp. Med. 1991; 174: 1617–1627
   PubMed Web of Science ®Google Scholar
• Wu L., Li C. L., Shortman K. Thymic dendritic cell precursors: relationship to the T lymphocyte lineage and phenotype of the dendritic cell progeny. J. Exp. Med. 1996; 184: 903–911
   PubMed Web of Science ®Google Scholar