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. 1998 Aug 1;102(3):606–618. doi: 10.1172/JCI3162

Nurse-like cells from bone marrow and synovium of patients with rheumatoid arthritis promote survival and enhance function of human B cells.

Y Shimaoka 1, J F Attrep 1, T Hirano 1, K Ishihara 1, R Suzuki 1, T Toyosaki 1, T Ochi 1, P E Lipsky 1
PMCID: PMC508921  PMID: 9691097

Abstract

Thymic nurse cells are known to interact with T cells and play a role in their functional maturation. However, the role of nurse cells in B cell maturation and differentiation is less well established, especially at extralymphoid sites. To address this issue, nurse-like cell clones from bone marrow and synovial tissue of patients with RA (RA-NLC) were established and characterized. RA-NLC constitutively expressed CD29, CD49c, CD54 (ICAM-1), CD106 (VCAM-1), CD157 (BST-1), and class I MHC molecules, and secreted IL-6, IL-7, IL-8, granulocyte-macrophage colony-stimulating factor (GM-CSF) and granulocyte colony-stimulating factor (G-CSF). Bone marrow-derived and synovial RA-NLC differed in that the former secreted IL-7 and expressed a greater density of CD157 constitutively and after stimulation with IFNgamma, whereas the latter secreted G-CSF and more IL-6. Stimulation of both bone marrow and synovial RA-NLC induced expression of CD40 and class II MHC, but not CD154 (CD40L) or CD35. RA-NLC rescued peripheral B cells from spontaneous apoptosis and promoted survival of B cells for > 4 wk. B cell survival was blocked by antibodies to CD106 or CD157. RA-NLC also increased Ig production from B cells. After long-term culture (4-6 wk) with RA-NLC, but not alone or with fibroblasts, outgrowth of B cells was observed. All B cell lines derived from these cultures had been transformed by EBV, although the RA-NLC themselves were not infected with EBV. Precursor frequency analysis indicated that approximately 1 in 12,500 peripheral B cells could give rise to these EBV-transformed B cell lines upon coculture with RA-NLC. These results indicate that RA-NLC from bone marrow and synovium have the capacity to rescue B cells from spontaneous apoptosis, facilitate Ig production, and promote the outgrowth of EBV-transformed B lymphoblastoid cells. These findings suggest that RA-NLC may play a role in the local and systemic hyperreactivity of B cells characteristic of rheumatoid arthritis.

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Selected References

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  1. Arnett F. C., Edworthy S. M., Bloch D. A., McShane D. J., Fries J. F., Cooper N. S., Healey L. A., Kaplan S. R., Liang M. H., Luthra H. S. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988 Mar;31(3):315–324. doi: 10.1002/art.1780310302. [DOI] [PubMed] [Google Scholar]
  2. Bosseloir A., Heinen E., Defrance T., Bouzhazha F., Antoine N., Simar L. J. Moabs MAS516 and 5B5, two fibroblast markers, recognize human follicular dendritic cells. Immunol Lett. 1994 Sep;42(1-2):49–54. doi: 10.1016/0165-2478(94)90034-5. [DOI] [PubMed] [Google Scholar]
  3. Clark E. A., Grabstein K. H., Gown A. M., Skelly M., Kaisho T., Hirano T., Shu G. L. Activation of B lymphocyte maturation by a human follicular dendritic cell line, FDC-1. J Immunol. 1995 Jul 15;155(2):545–555. [PubMed] [Google Scholar]
  4. Clark E. A., Grabstein K. H., Shu G. L. Cultured human follicular dendritic cells. Growth characteristics and interactions with B lymphocytes. J Immunol. 1992 Jun 1;148(11):3327–3335. [PubMed] [Google Scholar]
  5. Cocks B. G., de Waal Malefyt R., Galizzi J. P., de Vries J. E., Aversa G. IL-13 induces proliferation and differentiation of human B cells activated by the CD40 ligand. Int Immunol. 1993 Jun;5(6):657–663. doi: 10.1093/intimm/5.6.657. [DOI] [PubMed] [Google Scholar]
  6. Dechanet J., Merville P., Durand I., Banchereau J., Miossec P. The ability of synoviocytes to support terminal differentiation of activated B cells may explain plasma cell accumulation in rheumatoid synovium. J Clin Invest. 1995 Feb;95(2):456–463. doi: 10.1172/JCI117685. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Dong C., Wang J., Neame P., Cooper M. D. The murine BP-3 gene encodes a relative of the CD38/NAD glycohydrolase family. Int Immunol. 1994 Sep;6(9):1353–1360. doi: 10.1093/intimm/6.9.1353. [DOI] [PubMed] [Google Scholar]
  8. Dong C., Willerford D., Alt F. W., Cooper M. D. Genomic organization and chromosomal localization of the mouse Bp3 gene, a member of the CD38/ADP-ribosyl cyclase family. Immunogenetics. 1996;45(1):35–43. doi: 10.1007/s002510050164. [DOI] [PubMed] [Google Scholar]
  9. Edwards J. C., Leigh R. D., Cambridge G. Expression of molecules involved in B lymphocyte survival and differentiation by synovial fibroblasts. Clin Exp Immunol. 1997 Jun;108(3):407–414. doi: 10.1046/j.1365-2249.1997.4061306.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Edwards J. C., Wilkinson L. S., Speight P., Isenberg D. A. Vascular cell adhesion molecule 1 and alpha 4 and beta 1 integrins in lymphocyte aggregates in Sjögren's syndrome and rheumatoid arthritis. Ann Rheum Dis. 1993 Nov;52(11):806–811. doi: 10.1136/ard.52.11.806. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ferrero E., Malavasi F. Human CD38, a leukocyte receptor and ectoenzyme, is a member of a novel eukaryotic gene family of nicotinamide adenine dinucleotide+-converting enzymes: extensive structural homology with the genes for murine bone marrow stromal cell antigen 1 and aplysian ADP-ribosyl cyclase. J Immunol. 1997 Oct 15;159(8):3858–3865. [PubMed] [Google Scholar]
  12. Freedman A. S., Munro J. M., Rice G. E., Bevilacqua M. P., Morimoto C., McIntyre B. W., Rhynhart K., Pober J. S., Nadler L. M. Adhesion of human B cells to germinal centers in vitro involves VLA-4 and INCAM-110. Science. 1990 Aug 31;249(4972):1030–1033. doi: 10.1126/science.1697696. [DOI] [PubMed] [Google Scholar]
  13. Galdiero M., de l'Ero G. C., Marcatili A. Cytokine and adhesion molecule expression in human monocytes and endothelial cells stimulated with bacterial heat shock proteins. Infect Immun. 1997 Feb;65(2):699–707. doi: 10.1128/iai.65.2.699-707.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Gorczyca W., Gong J., Darzynkiewicz Z. Detection of DNA strand breaks in individual apoptotic cells by the in situ terminal deoxynucleotidyl transferase and nick translation assays. Cancer Res. 1993 Apr 15;53(8):1945–1951. [PubMed] [Google Scholar]
  15. Hiai H., Nishi Y., Miyazawa T., Matsudaira Y., Nishizuka Y. Mouse lymphoid leukemias: symbiotic complexes of neoplastic lymphocytes and their microenvironments. J Natl Cancer Inst. 1981 Apr;66(4):713–722. [PubMed] [Google Scholar]
  16. Hirata Y., Kimura N., Sato K., Ohsugi Y., Takasawa S., Okamoto H., Ishikawa J., Kaisho T., Ishihara K., Hirano T. ADP ribosyl cyclase activity of a novel bone marrow stromal cell surface molecule, BST-1. FEBS Lett. 1994 Dec 19;356(2-3):244–248. doi: 10.1016/0014-5793(94)01279-2. [DOI] [PubMed] [Google Scholar]
  17. 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 Sep;14(9):859–864. doi: 10.1002/eji.1830140916. [DOI] [PubMed] [Google Scholar]
  18. Ishihara K., Kobune Y., Okuyama Y., Itoh M., Lee B. O., Muraoka O., Hirano T. Stage-specific expression of mouse BST-1/BP-3 on the early B and T cell progenitors prior to gene rearrangement of antigen receptor. Int Immunol. 1996 Sep;8(9):1395–1404. doi: 10.1093/intimm/8.9.1395. [DOI] [PubMed] [Google Scholar]
  19. Ishikawa J., Kaisho T., Tomizawa H., Lee B. O., Kobune Y., Inazawa J., Oritani K., Itoh M., Ochi T., Ishihara K. Molecular cloning and chromosomal mapping of a bone marrow stromal cell surface gene, BST2, that may be involved in pre-B-cell growth. Genomics. 1995 Apr 10;26(3):527–534. doi: 10.1016/0888-7543(95)80171-h. [DOI] [PubMed] [Google Scholar]
  20. Itoh M., Ishihara K., Tomizawa H., Tanaka H., Kobune Y., Ishikawa J., Kaisho T., Hirano T. Molecular cloning of murine BST-1 having homology with CD38 and Aplysia ADP-ribosyl cyclase. Biochem Biophys Res Commun. 1994 Sep 15;203(2):1309–1317. doi: 10.1006/bbrc.1994.2325. [DOI] [PubMed] [Google Scholar]
  21. Itoh T., Doi H., Chin S., Nishimura T., Kasahara S. Establishment of mouse thymic nurse cell clones from a spontaneous BALB/c thymic tumor. Eur J Immunol. 1988 May;18(5):821–824. doi: 10.1002/eji.1830180525. [DOI] [PubMed] [Google Scholar]
  22. Iwabuchi K., Nakayama K., McCoy R. L., Wang F., Nishimura T., Habu S., Murphy K. M., Loh D. Y. Cellular and peptide requirements for in vitro clonal deletion of immature thymocytes. Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9000–9004. doi: 10.1073/pnas.89.19.9000. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Iwagami S., Furue S., Toyosaki T., Horikawa T., Doi H., Satomi S., Itoh T., Sakata T., Suzuki R. Establishment and characterization of nurse cell-like clones from human skin. Nurse cell-like clones can stimulate autologous mixed lymphocyte reaction. J Immunol. 1994 Oct 1;153(7):2927–2938. [PubMed] [Google Scholar]
  24. Jumper M. D., Splawski J. B., Lipsky P. E., Meek K. Ligation of CD40 induces sterile transcripts of multiple Ig H chain isotypes in human B cells. J Immunol. 1994 Jan 15;152(2):438–445. [PubMed] [Google Scholar]
  25. Kaisho T., Ishikawa J., Oritani K., Inazawa J., Tomizawa H., Muraoka O., Ochi T., Hirano T. BST-1, a surface molecule of bone marrow stromal cell lines that facilitates pre-B-cell growth. Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5325–5329. doi: 10.1073/pnas.91.12.5325. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Kajimoto Y., Miyagawa J., Ishihara K., Okuyama Y., Fujitani Y., Itoh M., Yoshida H., Kaisho T., Matsuoka T., Watada H. Pancreatic islet cells express BST-1, a CD38-like surface molecule having ADP-ribosyl cyclase activity. Biochem Biophys Res Commun. 1996 Feb 27;219(3):941–946. doi: 10.1006/bbrc.1996.0327. [DOI] [PubMed] [Google Scholar]
  27. Klein G. Epstein-Barr virus strategy in normal and neoplastic B cells. Cell. 1994 Jun 17;77(6):791–793. doi: 10.1016/0092-8674(94)90125-2. [DOI] [PubMed] [Google Scholar]
  28. Knecht H., Sahli R., Shaw P., Meyer C., Bachmann E., Odermatt B. F., Bachmann F. Detection of Epstein-Barr virus DNA by polymerase chain reaction in lymph node biopsies from patients with angioimmunoblastic lymphadenopathy. Br J Haematol. 1990 Aug;75(4):610–614. doi: 10.1111/j.1365-2141.1990.tb07807.x. [DOI] [PubMed] [Google Scholar]
  29. Koide J., Takada K., Sugiura M., Sekine H., Ito T., Saito K., Mori S., Takeuchi T., Uchida S., Abe T. Spontaneous establishment of an Epstein-Barr virus-infected fibroblast line from the synovial tissue of a rheumatoid arthritis patient. J Virol. 1997 Mar;71(3):2478–2481. doi: 10.1128/jvi.71.3.2478-2481.1997. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Koopman G., Parmentier H. K., Schuurman H. J., Newman W., Meijer C. J., Pals S. T. Adhesion of human B cells to follicular dendritic cells involves both the lymphocyte function-associated antigen 1/intercellular adhesion molecule 1 and very late antigen 4/vascular cell adhesion molecule 1 pathways. J Exp Med. 1991 Jun 1;173(6):1297–1304. doi: 10.1084/jem.173.6.1297. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Kriegsmann J., Keyszer G. M., Geiler T., Bräuer R., Gay R. E., Gay S. Expression of vascular cell adhesion molecule-1 mRNA and protein in rheumatoid synovium demonstrated by in situ hybridization and immunohistochemistry. Lab Invest. 1995 Feb;72(2):209–214. [PubMed] [Google Scholar]
  32. Lee B. O., Ishihara K., Denno K., Kobune Y., Itoh M., Muraoka O., Kaisho T., Sasaki T., Ochi T., Hirano T. Elevated levels of the soluble form of bone marrow stromal cell antigen 1 in the sera of patients with severe rheumatoid arthritis. Arthritis Rheum. 1996 Apr;39(4):629–637. doi: 10.1002/art.1780390414. [DOI] [PubMed] [Google Scholar]
  33. Lindhout E., Lakeman A., Mevissen M. L., de Groot C. Functionally active Epstein-Barr virus-transformed follicular dendritic cell-like cell lines. J Exp Med. 1994 Apr 1;179(4):1173–1184. doi: 10.1084/jem.179.4.1173. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Lindhout E., Mevissen M. L., Kwekkeboom J., Tager J. M., de Groot C. Direct evidence that human follicular dendritic cells (FDC) rescue germinal centre B cells from death by apoptosis. Clin Exp Immunol. 1993 Feb;91(2):330–336. doi: 10.1111/j.1365-2249.1993.tb05904.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Marlor C. W., Webb D. L., Bombara M. P., Greve J. M., Blue M. L. Expression of vascular cell adhesion molecule-1 in fibroblastlike synoviocytes after stimulation with tumor necrosis factor. Am J Pathol. 1992 May;140(5):1055–1060. [PMC free article] [PubMed] [Google Scholar]
  36. McNagny K. M., Bucy R. P., Cooper M. D. Reticular cells in peripheral lymphoid tissues express the phosphatidylinositol-linked BP-3 antigen. Eur J Immunol. 1991 Feb;21(2):509–515. doi: 10.1002/eji.1830210238. [DOI] [PubMed] [Google Scholar]
  37. McNagny K. M., Cazenave P. A., Cooper M. D. BP-3 alloantigen. A cell surface glycoprotein that marks early B lineage cells and mature myeloid lineage cells in mice. J Immunol. 1988 Oct 15;141(8):2551–2556. [PubMed] [Google Scholar]
  38. Miyake K., Hasunuma Y., Yagita H., Kimoto M. Requirement for VLA-4 and VLA-5 integrins in lymphoma cells binding to and migration beneath stromal cells in culture. J Cell Biol. 1992 Nov;119(3):653–662. doi: 10.1083/jcb.119.3.653. [DOI] [PMC free article] [PubMed] [Google Scholar]
  39. Morales-Ducret J., Wayner E., Elices M. J., Alvaro-Gracia J. M., Zvaifler N. J., Firestein G. S. Alpha 4/beta 1 integrin (VLA-4) ligands in arthritis. Vascular cell adhesion molecule-1 expression in synovium and on fibroblast-like synoviocytes. J Immunol. 1992 Aug 15;149(4):1424–1431. [PubMed] [Google Scholar]
  40. Mosmann T. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J Immunol Methods. 1983 Dec 16;65(1-2):55–63. doi: 10.1016/0022-1759(83)90303-4. [DOI] [PubMed] [Google Scholar]
  41. Muraoka O., Tanaka H., Itoh M., Ishihara K., Hirano T. Genomic structure of human BST-1. Immunol Lett. 1996 Dec 1;54(1):1–4. doi: 10.1016/s0165-2478(96)02633-8. [DOI] [PubMed] [Google Scholar]
  42. Nakajima-Iijima S., Hamada H., Reddy P., Kakunaga T. Molecular structure of the human cytoplasmic beta-actin gene: interspecies homology of sequences in the introns. Proc Natl Acad Sci U S A. 1985 Sep;82(18):6133–6137. doi: 10.1073/pnas.82.18.6133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Namen A. E., Lupton S., Hjerrild K., Wignall J., Mochizuki D. Y., Schmierer A., Mosley B., March C. J., Urdal D., Gillis S. Stimulation of B-cell progenitors by cloned murine interleukin-7. Nature. 1988 Jun 9;333(6173):571–573. doi: 10.1038/333571a0. [DOI] [PubMed] [Google Scholar]
  44. Newkirk M. M., Watanabe Duffy K. N., Leclerc J., Lambert N., Shiroky J. B. Detection of cytomegalovirus, Epstein-Barr virus and herpes virus-6 in patients with rheumatoid arthritis with or without Sjögren's syndrome. Br J Rheumatol. 1994 Apr;33(4):317–322. doi: 10.1093/rheumatology/33.4.317. [DOI] [PubMed] [Google Scholar]
  45. Okuyama Y., Ishihara K., Kimura N., Hirata Y., Sato K., Itoh M., Ok L. B., Hirano T. Human BST-1 expressed on myeloid cells functions as a receptor molecule. Biochem Biophys Res Commun. 1996 Nov 21;228(3):838–845. doi: 10.1006/bbrc.1996.1741. [DOI] [PubMed] [Google Scholar]
  46. Okuyama Y., Ishihara K., Kimura N., Hirata Y., Sato K., Itoh M., Ok L. B., Hirano T. Human BST-1 expressed on myeloid cells functions as a receptor molecule. Biochem Biophys Res Commun. 1996 Nov 21;228(3):838–845. doi: 10.1006/bbrc.1996.1741. [DOI] [PubMed] [Google Scholar]
  47. Pallesen G., Myhre-Jensen O. Immunophenotypic analysis of neoplastic cells in follicular dendritic cell sarcoma. Leukemia. 1987 Jul;1(7):549–557. [PubMed] [Google Scholar]
  48. Pezzano M., Li Y., Philp D., Omene C., Cantey M., Saunders G., Guyden J. C. Thymic nurse cell rescue of early CD4+CD8+ thymocytes from apoptosis. Cell Mol Biol (Noisy-le-grand) 1995 Dec;41(8):1099–1111. [PubMed] [Google Scholar]
  49. Pezzano M., Philp D., Stephenson S., Li Y., Reid V., Maitta R., Guyden J. C. Positive selection by thymic nurse cells requires IL-1 beta and is associated with an increased Bcl-2 expression. Cell Immunol. 1996 May 1;169(2):174–184. doi: 10.1006/cimm.1996.0108. [DOI] [PubMed] [Google Scholar]
  50. Prasad G. S., McRee D. E., Stura E. A., Levitt D. G., Lee H. C., Stout C. D. Crystal structure of Aplysia ADP ribosyl cyclase, a homologue of the bifunctional ectozyme CD38. Nat Struct Biol. 1996 Nov;3(11):957–964. doi: 10.1038/nsb1196-957. [DOI] [PubMed] [Google Scholar]
  51. Salmon M., Scheel-Toellner D., Huissoon A. P., Pilling D., Shamsadeen N., Hyde H., D'Angeac A. D., Bacon P. A., Emery P., Akbar A. N. Inhibition of T cell apoptosis in the rheumatoid synovium. J Clin Invest. 1997 Feb 1;99(3):439–446. doi: 10.1172/JCI119178. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Silvy A., Altevogt P., Mondière P., Bella C., Defrance T. A role for the VLA-4 integrin in the activation of human memory B cells. Eur J Immunol. 1997 Nov;27(11):2757–2764. doi: 10.1002/eji.1830271103. [DOI] [PubMed] [Google Scholar]
  53. Smiley J. D., Sachs C., Ziff M. In vitro synthesis of immunoglobulin by rheumatoid synovial membrane. J Clin Invest. 1968 Mar;47(3):624–632. doi: 10.1172/JCI105758. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Tohma S., Lipsky P. E. Analysis of the mechanisms of T cell-dependent polyclonal activation of human B cells. Induction of human B cell responses by fixed activated T cells. J Immunol. 1991 Apr 15;146(8):2544–2552. [PubMed] [Google Scholar]
  55. Tsunoda R., Nakayama M., Heinen E., Miyake K., Suzuki K., Sugai N., Kojima M. Emperipolesis of lymphoid cells by human follicular dendritic cells in vitro. Virchows Arch B Cell Pathol Incl Mol Pathol. 1992;62(2):69–78. doi: 10.1007/BF02899667. [DOI] [PubMed] [Google Scholar]
  56. Veale D. J., Maple C. Cell adhesion molecules in rheumatoid arthritis. Drugs Aging. 1996 Aug;9(2):87–92. doi: 10.2165/00002512-199609020-00003. [DOI] [PubMed] [Google Scholar]
  57. Vicari A. P., Bean A. G., Zlotnik A. A role for BP-3/BST-1 antigen in early T cell development. Int Immunol. 1996 Feb;8(2):183–191. doi: 10.1093/intimm/8.2.183. [DOI] [PubMed] [Google Scholar]
  58. Wekerle H., Ketelsen U. P., Ernst M. Thymic nurse cells. Lymphoepithelial cell complexes in murine thymuses: morphological and serological characterization. J Exp Med. 1980 Apr 1;151(4):925–944. doi: 10.1084/jem.151.4.925. [DOI] [PMC free article] [PubMed] [Google Scholar]
  59. Wekerle H., Ketelsen U. P. Thymic nurse cells--Ia-bearing epithelium involved in T-lymphocyte differentiation? Nature. 1980 Jan 24;283(5745):402–404. doi: 10.1038/283402a0. [DOI] [PubMed] [Google Scholar]
  60. Wernick R. M., Lipsky P. E., Marban-Arcos E., Maliakkal J. J., Edelbaum D., Ziff M. IgG and IgM rheumatoid factor synthesis in rheumatoid synovial membrane cell cultures. Arthritis Rheum. 1985 Jul;28(7):742–752. doi: 10.1002/art.1780280704. [DOI] [PubMed] [Google Scholar]
  61. Wysocki L. J., Sato V. L. "Panning" for lymphocytes: a method for cell selection. Proc Natl Acad Sci U S A. 1978 Jun;75(6):2844–2848. doi: 10.1073/pnas.75.6.2844. [DOI] [PMC free article] [PubMed] [Google Scholar]

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