LOCATION AND SEQUENCE OF REARRANGED IMMUNOGLOBULIN GENES IN HUMAN THYMUS

被引:39
作者
DUNNWALTERS, DK [1 ]
HOWE, CJ [1 ]
ISAACSON, PG [1 ]
SPENCER, J [1 ]
机构
[1] UCLMS, DEPT HISTOPATHOL, LONDON WC1E 6JJ, ENGLAND
基金
英国惠康基金;
关键词
IMMUNOGLOBULIN; THYMUS; B CELL; V-H GENE; SEQUENCE;
D O I
10.1002/eji.1830250231
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Thymic B cells are a proliferating B cell population concentrated in normal thymic medulla. They are large cells, some with dendritic morphology, and are not associated with any organized follicular structure. Previous work in this laboratory has shown that most of these B cells are surrounded by tightly adherent thymocytes. The literature on human thymic B cells contains many inconsistencies. There is no consensus on whether they express CD5. Even the existence of thymic B cells has been questioned. In this study we have undertaken the first analysis of rearranged immunoglobulin (Ig) genes, looking in particular for evidence of affinity maturation. The Ig V-H genes of human thymic B cells in this study are those of the fetal repertoire, though the resemblence to fetal Ig genes is limited in other respects. They are mostly unmutated, but the presence of mutated sequences suggests that this is not a uniform population, as has been previously indicated by phenotypic studies.
引用
收藏
页码:513 / 519
页数:7
相关论文
共 47 条
  • [1] THE USE OF CHROMOSOMAL TRANSLOCATIONS TO STUDY HUMAN-IMMUNOGLOBULIN GENE ORGANIZATION - MAPPING DH SEGMENTS WITHIN 35 KB OF THE C-MU GENE AND IDENTIFICATION OF A NEW DH LOCUS
    BULUWELA, L
    ALBERTSON, DG
    SHERRINGTON, P
    RABBITTS, PH
    SPURR, N
    RABBITTS, TH
    [J]. EMBO JOURNAL, 1988, 7 (07) : 2003 - 2010
  • [2] USE OF FAMILY SPECIFIC LEADER REGION PRIMERS FOR PCR AMPLIFICATION OF THE HUMAN HEAVY-CHAIN VARIABLE REGION GENE REPERTOIRE
    CAMPBELL, MJ
    ZELENETZ, AD
    LEVY, S
    LEVY, R
    [J]. MOLECULAR IMMUNOLOGY, 1992, 29 (02) : 193 - 203
  • [3] HUMAN-LYMPHOCYTES MAKING RHEUMATOID-FACTOR AND ANTIBODY TO SSDNA BELONG TO LEU-1+ B-CELL SUBSET
    CASALI, P
    BURASTERO, SE
    NAKAMURA, M
    INGHIRAMI, G
    NOTKINS, AL
    [J]. SCIENCE, 1987, 236 (4797) : 77 - 81
  • [4] CD5+ LYMPHOCYTE-B, POLYREACTIVE ANTIBODIES AND THE HUMAN B-CELL REPERTOIRE
    CASALI, P
    NOTKINS, AL
    [J]. IMMUNOLOGY TODAY, 1989, 10 (11): : 364 - 368
  • [5] THE CDR1 SEQUENCES OF A MAJOR PROPORTION OF HUMAN GERMLINE IG V-H GENES ARE INHERENTLY SUSCEPTIBLE TO AMINO-ACID REPLACEMENT
    CHANG, B
    CASALI, P
    [J]. IMMUNOLOGY TODAY, 1994, 15 (08): : 367 - 373
  • [6] MECHANISMS THAT GENERATE HUMAN-IMMUNOGLOBULIN DIVERSITY OPERATE FROM THE 8TH WEEK OF GESTATION IN FETAL LIVER
    CUISINIER, AM
    GAUTHIER, L
    BOUBLI, L
    FOUGEREAU, M
    TONNELLE, C
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (01) : 110 - 118
  • [7] DEANE M, 1991, LEUKEMIA, V5, P726
  • [8] DETECTION OF MONOCLONALITY IN LOW-GRADE B-CELL LYMPHOMAS USING THE POLYMERASE CHAIN-REACTION IS DEPENDENT ON PRIMER SELECTION AND LYMPHOMA TYPE
    DISS, TC
    PENG, HZ
    WOTHERSPOON, AC
    ISAACSON, PG
    PAN, LX
    [J]. JOURNAL OF PATHOLOGY, 1993, 169 (03) : 291 - 295
  • [9] THE MAJORITY OF HUMAN TONSILLAR CD5+ B-CELLS EXPRESS SOMATICALLY MUTATED V(CHI)4 GENES
    EBELING, SB
    SCHUTTE, MEM
    LOGTENBERG, T
    [J]. EUROPEAN JOURNAL OF IMMUNOLOGY, 1993, 23 (06) : 1405 - 1408
  • [10] EBELING SB, 1993, J IMMUNOL, V151, P6891