H2-M3(wt)-restricted, Listeria monocytogenes specific CD8 T cells recognize a novel, hydrophobic, protease-resistant, periodate-sensitive antigen

被引:35
作者
Nataraj, C
Brown, ML
Poston, RM
Shawar, SM
Rich, RR
Lindahl, KF
Kurlander, RJ
机构
[1] DUKE UNIV,MED CTR,DEPT MED,DURHAM,NC 27710
[2] DUKE UNIV,MED CTR,DEPT IMMUNOL,DURHAM,NC 27710
[3] BAYLOR COLL MED,DEPT MICROBIOL & IMMUNOL,HOUSTON,TX 77030
[4] BAYLOR COLL MED,DEPT MED,HOUSTON,TX 77030
[5] UNIV TEXAS,SW MED CTR,HOWARD HUGHES MED INST,DALLAS,TX 75235
[6] UNIV TEXAS,SW MED CTR,DEPT MICROBIOL,DALLAS,TX 75235
[7] UNIV TEXAS,SW MED CTR,DEPT BIOCHEM,DALLAS,TX 75235
关键词
antigen presentation; antigen-presenting cells; antigen processing; macrophage; MHC class l products; T cells;
D O I
10.1093/intimm/8.3.367
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mice infected with Listeria monocytogenes (LM) generate H2-M3(wt)-restricted CD8 effecters which recognize a heat-killed LM-associated antigen (HAA) presented by macrophages, To characterize HAA, we extracted a bioactive component from LM using SDS or NaOH. Extracted HAA aggregated in hydrophilic solvents but dissociated in the presence of SDS into a smaller subunit which migrated in Sephadex G-200 between chymotrypsinogen (25 kDa) and cytochrome c (12.5 kDa). HAA bioactivity and size was unaffected by proteinase K under conditions which degraded virtually all detectable protein, HAA was also unaffected by other proteases, RNase and DNase, but HAA bioactivity was destroyed by periodate, an agent that degrades carbohydrates. These studies demonstrate that H2-M3(wt) can present a hydrophobic, non-peptide, microbial antigen, probably glycolipid in origin, to CD8 T cells.
引用
收藏
页码:367 / 378
页数:12
相关论文
共 51 条
  • [21] SPECIALIZED ROLE FOR A MURINE CLASS-I-B MHC MOLECULE IN PROKARYOTIC HOST DEFENSES
    KURLANDER, RJ
    SHAWAR, SM
    BROWN, ML
    RICH, RR
    [J]. SCIENCE, 1992, 257 (5070) : 678 - 679
  • [22] MONOCLONAL-ANTIBODIES AGAINST RAT IMMUNOGLOBULIN KAPPA-CHAINS
    LANIER, LL
    GUTMAN, GA
    LEWIS, DE
    GRISWOLD, ST
    WARNER, NL
    [J]. HYBRIDOMA, 1982, 1 (02): : 125 - 131
  • [23] IDENTIFICATION OF A MONOCLONAL-ANTIBODY SPECIFIC FOR A MURINE T3 POLYPEPTIDE
    LEO, O
    FOO, M
    SACHS, DH
    SAMELSON, LE
    BLUESTONE, JA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (05) : 1374 - 1378
  • [24] LINDAHL KF, 1986, CURR TOP MICROBIOL, V127, P272
  • [25] LUKACS K, 1989, J IMMUNOL, V143, P3731
  • [26] T-CELL RECOGNITION OF CARBOHYDRATES ON TYPE-II COLLAGEN
    MICHAELSSON, E
    MALMSTROM, V
    REIS, S
    ENGSTROM, A
    BURKHARDT, H
    HOLMDAHL, R
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (02) : 745 - 749
  • [27] VACCINATION OF RHESUS-MONKEYS WITH SYNTHETIC PEPTIDE IN A FUSOGENIC PROTEOLIPOSOME ELICITS SIMIAN IMMUNODEFICIENCY VIRUS-SPECIFIC CD8+ CYTOTOXIC LYMPHOCYTES-T
    MILLER, MD
    GOULDFOGERITE, S
    SHEN, L
    WOODS, RM
    KOENIG, S
    MANNINO, RJ
    LETVIN, NL
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) : 1739 - 1744
  • [28] INTRODUCTION OF SOLUBLE-PROTEIN INTO THE CLASS-I PATHWAY OF ANTIGEN PROCESSING AND PRESENTATION
    MOORE, MW
    CARBONE, FR
    BEVAN, MJ
    [J]. CELL, 1988, 54 (06) : 777 - 785
  • [29] DIFFERENCES IN ANTIGEN PRESENTATION TO MHC CLASS-I-RESTRICTED AND CLASS-II-RESTRICTED INFLUENZA VIRUS-SPECIFIC CYTOLYTIC LYMPHOCYTE-T CLONES
    MORRISON, LA
    LUKACHER, AE
    BRACIALE, VL
    FAN, DP
    BRACIALE, TJ
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1986, 163 (04) : 903 - 921
  • [30] PROPERTIES OF THE SCRAPIE PRION PROTEIN - QUANTITATIVE-ANALYSIS OF PROTEASE RESISTANCE
    OESCH, B
    JENSEN, M
    NILSSON, P
    FOGH, J
    [J]. BIOCHEMISTRY, 1994, 33 (19) : 5926 - 5931