Identical expression of CD45R isoforms by CD45RC(+) 'revertant' memory and CD45RC(+) naive CD4 T cells

被引:43
作者
Hargreaves, M [1 ]
Bell, EB [1 ]
机构
[1] UNIV MANCHESTER, SCH MED, IMMUNOL RES GRP, MANCHESTER M13 9PT, LANCS, ENGLAND
关键词
D O I
10.1046/j.1365-2567.1997.00267.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Naive and memory CD4 T cells are frequently defined by exon-specific monoclonal antibodies (mAb) which stain (or not) high- or low-molecular-weight (MW) isoforms of the leucocyte common antigen CD45. The link between isoform and the naive/memory designation is complicated by the fact that CD4 T cells with a 'memory' phenotype (CD45RA(-), RB-, RC-, or CD45RO(+)) may revert ('revertants') and re-express the high mw isoform (CD45RA(+), RB+, RC+). Isoform expression also changes during normal T-cell development. Furthermore, the picture may be incomplete since an exon-specific mAb will not detect all possible isoforms on a cell. We have used molecular techniques to determine whether revertant CD4 memory T cells were different from naive T cells with respect to CD45R isoform expression. Using the anti-CD45RC mAb OX22 to purify rat lymphocyte subsets, CD45R isoform expression was examined at the mRNA level in CD4 T cells at different stages of development and compared with that of B cells and unseparated lymphocytes. B cells contained abundant message for the highest MW 3-exon isoform ABC, the 2-exon isoforms AB and BC, and the null isoform O. Both immature CD45RC(-) (i.e. CD4(+)8(-) 'single positive' thymocytes, and peripheral Thy-1(+) recent thymic emigrants) and mature CD45RC(-) 'antigen-experienced' CD4 T cells had message for single-exons B, possibly C and for the O exon. In contrast, CD45RC(+) CD4 T cells contained mRNA coding for ABC (low level), AB, BC, B, C (low level) and O (low level), Importantly, there was no difference between CD45RC(+) T cells that had not seen antigen ('truly naive') and CD45RC(+) antigen-experienced revertant memory T cells. This observation has implications for understanding long-term immunological memory.
引用
收藏
页码:323 / 330
页数:8
相关论文
共 51 条
[11]   CD45RC isoforms define two types of CD4 memory T cells, one of which depends on persisting antigen [J].
Bunce, C ;
Bell, EB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (04) :767-776
[12]  
BYRNE JA, 1988, J IMMUNOL, V141, P3249
[13]   THE ROLE OF PROTEIN-TYROSINE KINASES AND PROTEIN-TYROSINE PHOSPHATASES IN T-CELL ANTIGEN RECEPTOR SIGNAL-TRANSDUCTION [J].
CHAN, AC ;
DESAI, DM ;
WEISS, A .
ANNUAL REVIEW OF IMMUNOLOGY, 1994, 12 :555-592
[14]  
CLEMENT LT, 1988, J IMMUNOL, V141, P1464
[15]   ANTIGENIC DETERMINANTS ENCODED BY ALTERNATIVELY SPLICED EXONS OF CD45 ARE DETERMINED BY THE POLYPEPTIDE BUT INFLUENCED BY GLYCOSYLATION [J].
CYSTER, JG ;
FOWELL, D ;
BARCLAY, AN .
INTERNATIONAL IMMUNOLOGY, 1994, 6 (12) :1875-1881
[16]  
HATHCOCK KS, 1992, J IMMUNOL, V148, P19
[17]  
HOSSEINZADEH H, 1993, J IMMUNOL, V150, P1670
[18]   THE EXTRA SEGMENTS OF SEQUENCE IN RAT LEUKOCYTE COMMON ANTIGEN (L-CA) ARE DERIVED BY ALTERNATIVE SPLICING OF ONLY 3 EXONS AND SHOW EXTENSIVE O-LINKED GLYCOSYLATION [J].
JACKSON, DI ;
BARCLAY, AN .
IMMUNOGENETICS, 1989, 29 (05) :281-287
[19]   IDENTIFICATION OF THE ALTERNATIVELY SPLICED EXONS OF MURINE CD45 (T200) REQUIRED FOR REACTIVITY WITH B220 AND OTHER T200-RESTRICTED ANTIBODIES [J].
JOHNSON, P ;
GREENBAUM, L ;
BOTTOMLY, K ;
TROWBRIDGE, IS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (03) :1179-1184
[20]   THE COEXPRESSION OF CD45RA AND CD45RO ISOFORMS ON T-CELLS DURING THE S/G2/M STAGES OF CELL-CYCLE [J].
LASALLE, JM ;
HAFLER, DA .
CELLULAR IMMUNOLOGY, 1991, 138 (01) :197-206