Lifespan of γ/δ T cells

被引:92
作者
Tough, DF [1 ]
Sprent, J [1 ]
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
关键词
D O I
10.1084/jem.187.3.357
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Information on the turnover and lifespan of murine gamma/delta cells was obtained by administering the DNA precursor, bromodeoxyuridine (BrdU), in the drinking water and staining lymphoid cells for BrdU incorporation. For TCR-gamma/delta (V gamma 2) transgenic mice, nearly all gamma/delta thymocytes became BrdU(+) within 2 d and were released rapidly into the peripheral lymphoid tissues. These recent thymic emigrants (RTEs) underwent phenotypic maturation in the periphery for several days, but most of these cells died within 4 wk. In adult thymectomized (ATx) transgenic mice, only a small proportion of gamma/delta cells survived as long-lived cells; most of these cells had a slow turnover and retained a naive phenotype. As in transgenic mice, the majority of RTEs generated in normal mice (C57BL/6) appeared to have a restricted lifespan as naive cells. However, in marked contrast to TCR transgenic mice, most of the gamma/delta cells surviving in ATx normal mice had a rapid turnover and displayed an activated/memory phenotype, implying a chronic response to environmental antigens. Hence, in normal mice many gamma/delta RTEs did not die but switched to memory cells.
引用
收藏
页码:357 / 365
页数:9
相关论文
共 45 条
[31]   THE NATURE OF MAJOR HISTOCOMPATIBILITY COMPLEX RECOGNITION BY GAMMA-DELTA-T-CELLS [J].
SCHILD, H ;
MAVADDAT, N ;
LITZENBERGER, C ;
EHRICH, EW ;
DAVIS, MM ;
BLUESTONE, JA ;
MATIS, L ;
DRAPER, RK ;
CHIEN, YH .
CELL, 1994, 76 (01) :29-37
[32]   Positive selection is not required for thymic maturation of transgenic gamma delta T cells [J].
Schweighoer, E ;
Fowlkes, BJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2033-2041
[33]   INDUCTION OF MURINE PERITONEAL GAMMA-DELTA-T-CELLS AND THEIR ROLE IN RESISTANCE TO BACTERIAL-INFECTION [J].
SKEEN, MJ ;
ZIEGLER, HK .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (03) :971-984
[34]   GAMMA-DELTA-T-CELLS DIFFERENTIATE INTO A FUNCTIONAL BUT NONPROLIFERATIVE STATE DURING A NORMAL IMMUNE-RESPONSE [J].
SPANER, D ;
MIGITA, K ;
OCHI, A ;
SHANNON, J ;
MILLER, RG ;
PEREIRA, P ;
TONEGAWA, S ;
PHILLIPS, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (18) :8415-8419
[35]   Immunological memory [J].
Sprent, J .
CURRENT OPINION IN IMMUNOLOGY, 1997, 9 (03) :371-379
[36]   PROPERTIES OF PURIFIED T-CELL SUBSETS .1. INVITRO RESPONSES TO CLASS-I VS CLASS-II H-2 ALLOANTIGENS [J].
SPRENT, J ;
SCHAEFER, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (06) :2068-2088
[37]  
TAKADA H, 1993, J IMMUNOL, V151, P2062
[38]   NATURAL AND SYNTHETIC NONPEPTIDE ANTIGENS RECOGNIZED BY HUMAN GAMMA-DELTA T-CELLS [J].
TANAKA, Y ;
MORITA, CT ;
TANAKA, Y ;
NIEVES, E ;
BRENNER, MB ;
BLOOM, BR .
NATURE, 1995, 375 (6527) :155-158
[39]   TURNOVER OF NAIVE-PHENOTYPE AND MEMORY-PHENOTYPE T-CELLS [J].
TOUGH, DF ;
SPRENT, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 179 (04) :1127-1135
[40]   Induction of bystander T cell proliferation by viruses and type I interferon in vivo [J].
Tough, DF ;
Borrow, P ;
Sprent, J .
SCIENCE, 1996, 272 (5270) :1947-1950