Chinese goose (Anser cygnoides) CD8a: Cloning, tissue distribution and immunobiological in splenic mononuclear cells

Gene

Volumn 529, Issue 2, 2013, Pages 332-339

  Zhao, Qiurong ^a   Liu, Fei ^a   Chen, Shun ^a   Yan, Xiaoling ^a   Qi, Yulin ^a   Wang, Mingshu ^a   Jia, Renyong ^a   Zhu, Dekang ^a   Liu, Mafeng ^a   Chen, Xiaoyue ^a   Cheng, Anchun ^a  

^a SICHUAN AGRICULTURAL UNIVERSITY   (China)

Author keywords

CD8 ; Goose; Immunobiological activity; Molecular cloning; NGVEV infection; Tissue distribution

Indexed keywords

CD8ALPHA ANTIGEN; COMPLEMENTARY DNA; MESSENGER RNA; PHYTOHEMAGGLUTININ;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIRD DISEASE; BURSA FABRICII; CECUM; CELLULAR IMMUNITY; CONTROLLED STUDY; ENTERITIS; GOOSE; GOSLING; IMMUNOBIOLOGY; IN VITRO STUDY; MOLECULAR CLONING; MONONUCLEAR CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; OPEN READING FRAME; PHYLOGENY; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SPLEEN; THYMUS; TISSUE DISTRIBUTION; UPREGULATION;

AAP; ABRIDGED ANCHOR PRIMER; ABRIDGED UNIVERSAL AMPLIFICATION PRIMER; ADAPTER PRIMER; AP; AUAP; BASIC LOCAL ALIGNMENT SEARCH TOOL; BF; BLAST; BURSA OF FABRICIUS; CD8Α; CDNA; CECAL TONSIL; CELL-MEDIATED CYTOTOXICITY; CELL-MEDIATED IMMUNE; CHCD8Α; CHICKEN CD8Α; CIS; CMC; CMI; COMPLEMENTARY TO RNA; CT; CTLS; CUTANEOUS IMMUNE SYSTEM; CYTOTOXIC T LYMPHOCYTES; GENE SPECIFIC PRIMER; GOCD8Α; GOOSE; GOOSE CD8Α; GSP; HARDERIAN GLAND; HG; IEL; IMMUNOBIOLOGICAL ACTIVITY; INTESTINAL INTRAEPITHELIAL LYMPHOCYTES; LD(50); LETHAL DOSE; LIPOPOLYSACCHARIDE; LPS; MAJOR HISTOCOMPATIBILITY COMPLEX; MHC; MIS; MNCS; MOLECULAR CLONING; MONOCOLOR CELLS; MUCOSAL IMMUNE SYSTEM; NEW TYPE GOSLING VIRAL ENTERITIS VIRUS; NGVEV; NGVEV INFECTION; OFR; OPEN READING FRAME; PHA; PHYTOHEMAGGLUTININ; PI; POST INFECTION; QPCR; QUANTITATIVE PCR; RACE; RAPID AMPLIFICATION OF CDNA ENDS; REVERSE TRANSCRIPTION-POLYMERASE CHAIN REACTION; RT-PCR; T CELL ANTIGEN RECEPTOR; TCID50; TCR; TISSUE CULTURE INFECTIVE DOSE; TISSUE DISTRIBUTION; TUCD8Α; TURKEY CD8Α; UNTRANSLATED REGION; UTR;

AMINO ACID SEQUENCE; ANIMALS; ANTIGENS, CD8; AVIAN PROTEINS; BASE SEQUENCE; CECUM; CLONING, MOLECULAR; GEESE; LEUKOCYTES, MONONUCLEAR; LIPOPOLYSACCHARIDES; MOLECULAR SEQUENCE DATA; ORGAN SPECIFICITY; PARVOVIRIDAE; PHYTOHEMAGGLUTININS; RNA, MESSENGER; SPLEEN; THYMUS GLAND; TISSUE DISTRIBUTION; TRANSCRIPTION, GENETIC;

ANATIDAE; ANSER; ANSER CYGNOIDES; AVES;

EID: 84883826218     PISSN: 03781119     EISSN: 18790038     Source Type: Journal    
DOI: 10.1016/j.gene.2013.07.104     Document Type: Article

References (42)

1. Andersson J., Coutinho A., Lernhardt W., Melchers F. Clonal growth and maturation to immunoglobulin secretion in vitro of every growth-inducible B lymphocyte. Cell 1977, 10:27-34.
2. Barry M., Bleackley R.C. Cytotoxic T lymphocytes: all roads lead to death. Nat. Rev. Immunol. 2002, 2:401-409.
3. Bertram E.M., Jilbert A., Kotlarski I. An homologous in vitro assay to detect lymphokines released by PHA-activated duck peripheral blood lymphocytes and spleen cells. Vet. Immunol. Immunopathol. 1997, 56:163-174.
4. Bos J.D., Kapsenberg M.L. The skin immune system: progress in cutaneous biology. Immunol. Today 1993, 14:75-78.
5. Brandtzaeg P. Overview of the mucosal immune system. Curr. Top. Microbiol. Immunol. 1989, 146:13-25.
6. Bromley S.K., Thomas S.Y., Luster A.D. Chemokine receptor CCR7 guides T cell exit from peripheral tissues and entry into afferent lymphatics. Nat. Immunol. 2005, 6:895-901.
7. Chen S., Cheng A., Wang M. Studies on adaptation of NGVEV in duck embryo fibroblasts and multiplication characteristic. Vet. Sci. China 2006, 36:773-778.
8. Chen S., Cheng A.C., Wang M.S. Morphologic observations of new type gosling viral enteritis virus (NGVEV) virulent isolate in infected duck embryo fibroblasts. Avian Dis. 2008, 52:173-178.
9. Chen S., Cheng A.C., Wang M.S., Peng X. Detection of apoptosis induced by new type gosling viral enteritis virus in vitro through fluorescein annexin V-FITC/PI double labeling. World J. Gastroenterol. 2008, 14:2174-2178.
10. Cheng A.C., Wang M.S., Chen X.Y., Guo Y.F., Liu Z.Y., Fang P.F. Pathogenic and pathological characteristic of new type gosling viral enteritis first observed in China. World J. Gastroenterol. 2001, 7:678-684.
11. Cooper S., et al. Analysis of a successful immune response against hepatitis C virus. Immunity 1999, 10(4):439-449.
12. De Totero D., et al. Heterogeneous immunophenotype of granular lymphocyte expansions: differential expression of the CD8 alpha and CD8 beta chains [see comments]. Blood 1992, 80:1765-1773.
13. DiSanto J.P., Knowles R.W., Flomenberg N. The human Lyt-3 molecule requires CD8 for cell surface expression. EMBO J. 1988, 7:3465-3470.
14. + T cell exhaustion versus memory. Immunity 2012, 37:1130-1144.
15. Emmrich F., Kanz L., Eichmann K. Cross-linking of the T cell receptor complex with the subset-specific differentiation antigen stimulates interleukin 2 receptor expression in human CD4 and CD8 T cells. Eur. J. Immunol. 1987, 17:529-534.
16. Gibbings D.J., Marcet-Palacios M., Sekar Y., Ng M.C.Y., Befus A.D. CD8α is expressed by human monocytes and enhances FcγR-dependent responses. BMC Immunol. 2007, 8:12.
17. + T cell effector mechanisms in resistance to infection. Annu. Rev. Immunol. 2000, 18:275-308.
18. Higgins D., Teoh C.S.H. Duck lymphocytes II. Culture conditions for optimum transformation response to phytohaemagglutinin. J. Immunol. Methods 1988, 106:135-145.
19. Hwang E.S., Park C.G., Cha C.Y. Immune responses to viral infection. Immune Netw. 2004, 4:73-80.
20. Jarry A., Cerf-bensussan N., Brousse N., Selz F., Guy-grand D. Subsets of CD3+ (T cell receptor α/β or γ/δ) and CD3- lymphocytes isolated from normal human gut epithelium display phenotypical features different from their counterparts in peripheral blood. Eur. J. Immunol. 1990, 20:1097-1103.
21. Johnson H.L., et al. CD8 T cell-initiated blood-brain barrier disruption is independent of neutrophil support. J. Immunol. 2012, 189:1937-1945.
22. Kägi D., et al. Fas and perforin pathways as major mechanisms of T cell-mediated cytotoxicity. Science (New York, N.Y.) 1994, 265:528-530.
23. Kavathas P., Sukhatme V.P., Herzenberg L.A., Parnes J.R. Isolation of the gene encoding the human T-lymphocyte differentiation antigen Leu-2 (T8) by gene transfer and cDNA subtraction. Proc. Natl. Acad. Sci. 1984, 81:7688-7692.
24. Kida H., Yanagawa R., Matsuoka Y. Duck influenza lacking evidence of disease signs and immune response. Infect. Immun. 1980, 30:547-553.
25. Kitchen S.G., et al. The CD4 molecule on CD8+ T lymphocytes directly enhances the immune response to viral and cellular antigens. Proc. Natl. Acad. Sci. U. S. A. 2005, 102:3794-3799.
26. König R., Ronald N.G. MHC class II interaction with CD4 mediated by a region analogous to the MHC class I binding site for CD8. Nature 1992, 356:796-798.
27. Kothlow S., Mannes N.K., Schaerer B., Rebeski D.E., Kaspers B., Schultz U. Characterization of duck leucocytes by monoclonal antibodies. Dev. Comp. Immunol. 2005, 29:733-748.
28. Matthews P.C., et al. Co-operative additive effects between HLA alleles in control of HIV-1. PLoS One 2012, 7:e47799.
29. McGhee J.R., Mestecky J., Dertzbaugh M.T., Eldridge J.H., Hirasawa M., Kiyono H. The mucosal immune system: from fundamental concepts to vaccine development. Vaccine 1992, 10:75-88.
30. Norment A.M., Littman D. A second subunit of CD8 is expressed in human T cells. EMBO J. 1988, 7:3433-3439.
31. Pardo J., et al. The biology of cytotoxic cell granule exocytosis pathway: granzymes have evolved to induce cell death and inflammation. Microbes Infect. 2009, 11(4):452-459.
32. Powell F., Lawson M., Rothwell L., Kaiser P. Development of reagents to study the turkey's immune response: identification and molecular cloning of turkey CD4, CD8α and CD28. Dev. Comp. Immunol. 2009, 33:540-546.
33. Reimann J., Rudolphi A. Co-expression of CD8α in CD4+ T cell receptor αβ+ T cells migrating into the murine small intestine epithelial layer. Eur. J. Immunol. 2005, 25:1580-1588.
34. Salter R.D., et al. A binding site for the T-cell co-receptor CD8 on the α3 domain of HLA-A2. Nature 1990, 345:41-46.
35. Sansonno D. Immune-related disorders and extrahepatic diseases in chronic HCV infection. Clin. Dev. Immunol. 2012, 2012:509309.
36. Sung J.M., Lee C.K., Wu-Hsieh B.A. Intrahepatic infiltrating NK and CD8 T cells cause liver cell death in different phases of dengue virus infection. PLoS One 2012, 7:e46292.
37. Tamura K., Dudley J., Nei M., Kumar S. MEGA4: molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol. Biol. Evol. 2007, 24:1596-1599.
38. Tregaskes C., et al. Identification and analysis of the expression of CD8 alpha beta and CD8 alpha alpha isoforms in chickens reveals a major TCR-gamma delta CD8 alpha beta subset of intestinal intraepithelial lymphocytes. J. Immunol. 1995, 154:4485-4494.
39. Vremec D., Pooley J., Hochrein H., Wu L., Shortman K. CD4 and CD8 expression by dendritic cell subtypes in mouse thymus and spleen. J. Immunol. 2000, 164:2978-2986.
40. Xu S., Wu J., Hu K., Ping H., Duan Z., Zhang H. Molecular cloning and expression of orange-spotted grouper (Epinephelus coioides) CD8α and CD8β genes. Fish Shellfish Immunol. 2011, 30:600-608.
41. Yan X.L., et al. Molecular cloning, characterization and tissue expression of CD4 in Chinese goose. Gene 2013, 519(2):298-304.
42. Zamoyska R. The CD8 coreceptor revisited: one chain good, two chains better. Immunity 1994, 1:243-246.