Peritoneal T lymphocyte regulation by macrophages

Immunobiology

Volumn 216, Issue 1-2, 2011, Pages 256-264

  Composto, G ^a   Gonzalez, D ^a   Bucknum, A ^b   Silberman, D ^c   Taylor, J ^d   Kozlowski, M ^e   Bloomfield, T ^f   Bartlett, T ^a   Riggs, J ^a  

^a RIDER UNIVERSITY   (United States)

^b Molecular Diagnostics Laboratory   (United States)

^c TEMPLE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d NATIONAL JEWISH MEDICAL AND RESEARCH CENTER   (United States)

^e UNIVERSITY OF PENNSYLVANIA   (United States)

^f KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

Macrophages; Peritoneal; Suppression; T cells

Indexed keywords

ARGININE; CD3 ANTIGEN; CD45RB ANTIGEN; GAMMA INTERFERON; GLUCOCORTICOID INDUCED TUMOR NECROSIS FACTOR RECEPTOR; HERMES ANTIGEN; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 2 RECEPTOR ALPHA; L SELECTIN; TRANSCRIPTION FACTOR FOXP3;

AMINO ACID METABOLISM; ANIMAL CELL; ARTICLE; BAGG ALBINO MOUSE; C57BL 6 MOUSE; CD25+ T LYMPHOCYTE; CD4 CD8 RATIO; CONTROLLED STUDY; CYTOKINE PRODUCTION; DBA 2 MOUSE; FEMALE; IMMUNOREGULATION; IN VITRO STUDY; LYMPH NODE; MACROPHAGE; MALE; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REGULATORY T LYMPHOCYTE; SPLEEN; STRAIN DIFFERENCE; T LYMPHOCYTE; T LYMPHOCYTE ACTIVATION;

ANIMALS; CD4-POSITIVE T-LYMPHOCYTES; CD8-POSITIVE T-LYMPHOCYTES; CELL COMMUNICATION; CELLS, CULTURED; FORKHEAD TRANSCRIPTION FACTORS; IMMUNE TOLERANCE; IMMUNOLOGIC MEMORY; INTERLEUKIN-2 RECEPTOR ALPHA SUBUNIT; MACROPHAGES, PERITONEAL; MICE; MICE, INBRED STRAINS; MICE, MUTANT STRAINS; RECEPTORS, NERVE GROWTH FACTOR; RECEPTORS, TUMOR NECROSIS FACTOR; T-LYMPHOCYTES, REGULATORY;

EID: 78649500813     PISSN: 01712985     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.imbio.2010.04.002     Document Type: Article

References (36)

1. Ansel K., Harris R., Cyster J. CXCL13 is required for B1 cell homing, natural antibody production, and body cavity immunity. Immunity 2002, 16:67-76.
2. + T cell proliferation via an IFN-γ and nitric oxide-dependent mechanism. J. Immunol. 2001, 167:4293-4302.
3. Boldizsar F., Tarjanyi O., Nemeth P., Mikecz K., Giant T. Th1/Th17 polarization and acquisition of an arthritogenic phenotype in arthritis-susceptible BALB/c, but not in MHC-matched, arthritis-resistant DBA/2 mice. Int. Immunol. 2009, 21:511-522.
4. Carlow D., Gold M., Ziltener H. Lymphocytes in the peritoneum home to the omentum and are activated by resident dendritic cells. J. Immunol. 2009, 183:1155-1165.
5. Davies J., Gordon S. Isolation and culture of murine macrophages. Meth. Mol. Biol. 2005, 290:91-103.
6. Festing M., Legg R., Eydmann T., Brammall A. Mouse strain differences in resident peritoneal cells: a flow cytometric analysis. Lab. Anim. 1990, 24:53-62.
7. Fontenot J., Rudensky A. A well adapted regulatory contrivance: regulatory T cell development and the forkhead family transcription factor Foxp3. Nat. Immunol. 2005, 6:331-337.
8. Fortier A. Activation of Murine Macrophages. Current Protocols in Immunology 2001, May, Chapter 14, Unit 14.4.
9. Gabrilovitch D., Nagaraj S. Myeloid-derived suppressor cells as regulators of the immune system. Nat. Rev. Immunol. 2009, 9:162-174.
10. + T cells. Curr. Opin. Immunol. 2003, 15:690-696.
11. Geissman F., Jung S., Littman D. Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity 2003, 19:71-82.
12. Hardy R. B-1 B cells: development, selection, natural autoantibody and leukemia. Curr. Opin. Immunol. 2006, 18:547-555.
13. Hayakawa K., Hardy R., Honda M., Herzenberg L.A., Steinberg A. Ly-1 B cells: functionally distinct lymphocytes that secrete IgM autoantibodies. Proc. Natl. Acad. Sci. U.S.A. 1984, 81:2494-2498.
14. Hoerauf A., Solbach W., Lohoff M., Rollinghoff M. The Xid defect determines an improved clinical course of murine leishmaniasis in susceptible mice. Int. Immunol. 1994, 6:1117-1127.
15. Kamei M., Carman C. New observations on the trafficking and diapedesis of monocytes. Curr. Opin. Hematol. 2010, 17:43-52.
16. LaGasse E., Weissman I. Flow cytometric identification of murine neutrophils and monocytes. J. Immunol. Meth. 1996, 197:139-150.
17. Mackay C., von Andrian U. Memory T cells - local heroes in the struggle for immunity. Science 2001, 291:2323-2324.
18. Masopust D., Vezys V., Marzo A., Lefrancois L. Preferential localization of effector memory cells in nonlymphoid tissue. Science 2001, 291:2413-2417.
19. Matlack R., Yeh K., Rosini L., Gonzalez D., Taylor J., Silberman D., Pennello A., Riggs J. Peritoneal macrophages suppress T cell activation by amino acid catabolism. Immunology 2006, 117:386-395.
20. + regulatory T cells in mice infected with the filarial parasite Brugia malayi. J. Immunol. 2008, 181:6456-6466.
21. Popi A., Lopes J., Mariano M. Interleukin-10 secreted by B-1 cells modulates the phagocytic activity of murine macrophages in vitro. Macrophages from wild-type mice have a lower ability to release nitric oxide and hydrogen peroxide when compared with macrophages from Xid mice. Immunology 2004, 113:348-358.
22. Rangel-Moreno J., Moyron-Quiroz J., Carragher D., Kusser K., Hartson L., Moquin A., Randall T. Omental milky spots develop in the absence of lymphoid tissue-inducer cells and support B and T cell responses to peritoneal antigens. Immunity 2009, 30:731-740.
23. Reinhardt R., Khoruts A., Merica R., Zell T., Jenkins M. Visualizing the generation of memory CD4 T cells in the whole body. Nature 2001, 410:101-105.
24. Riggs J., Howell K., Taylor J., Mahjied T., Prokopenko N., Alvarez J., Coleman C. Mls presentation by peritoneal cavity B cells. Immunobiology 2004, 209:255-264.
25. Rosini L., Matlack R., Taylor J., Howell K., Yeh K., Pennello A., Riggs J. Nonlymphoid peritoneal cells suppress the T cell response to Mls. Immunobiology 2004, 209:575-584.
26. Shimizu T., Sano C., Tomioka H. The role of B7 molecules in the cell contact-mediated suppression of T cell mitogenesis by immunosuppressive macrophages induced with mycobacterial infection. Clin. Exp. Immunol. 2004, 135:373-379.
27. Silberman D., Bucknum A., Kozlowski M., Matlack R., Riggs J. Cytokine treatment of macrophage suppression of T cell activation. Immunobiology 2010, 215:70-80.
28. Solvason N., Lehuenm A., Kearney J. An embryonic source of Ly1 but not conventional B cells. Int. Immunol. 1991, 3:543-550.
29. Stadler B., de Week A. Flow cytometric analysis of mouse peritoneal macrophages. Cell. Immunol. 1980, 54:36-48.
30. + T cell hyporesponsiveness at sites peripheral to filarial infection. J. Immunol. 2006, 176:6918-6927.
31. Turchyn L., Baginski T., Renkiewicz R., Lesch C., Mobley J. Phenotypic and functional analysis of murine resident and induced peritoneal macrophages. Comp. Med. 2007, 57:574-580.
32. Turley S., Lee J.-W., Dutton-Swain N., Mathis D., Benoist C. Endocrine self and gut non-self intersect in the pancreatic lymph nodes. Proc. Natl. Acad. Sci. 2005, 102:17729-17733.
33. Vaarala O., Atkinson M., Neu J. The "perfect storm" for type 1 diabetes: the complex interplay between intestinal microbiota, gut permeability, and mucosal immunity. Diabetes 2008, 57:2555-2562.
34. + T cells in vivo. J. Immunol. 2009, 182:7490-7500.
35. Walsh K., Brady M., Finlay C., Boon L., Mills K. Infection with a helminth parasite attenuates autoimmunity through TGF-β-mediated suppression of Th17 and Th1 responses. J. Immunol. 2009, 183:1577-1586.
36. Williams R., White H. The greater omentum: its applicability to cancer surgery and cancer therapy. Curr. Probl. Surg. 1986, 23:789-865.