CHARACTERIZATION OF C-KIT POSITIVE INTRATHYMIC STEM-CELLS THAT ARE RESTRICTED TO LYMPHOID DIFFERENTIATION

被引:207
作者
MATSUZAKI, Y
GYOTOKU, J
OGAWA, M
NISHIKAWA, S
KATSURA, Y
GACHELIN, G
NAKAUCHI, H
机构
[1] INST PHYS & CHEM RES,CELL GROWTH & DIFFERENTIAT LAB,3-1-1 KOYADAI,TSUKUBA 305,JAPAN
[2] KUMAMOTO UNIV,SCH MED,INST MOLEC EMBRYOL & GENET,KUMAMOTO 860,JAPAN
[3] UNIV TSUKUBA,SCH MED,TSUKUBA 305,JAPAN
[4] KYOTO UNIV,CHEST DIS RES INST,DEPT IMMUNOL,KYOTO 606,JAPAN
[5] INST PASTEUR,UNITE BIOL MOLEC GENE,F-75724 PARIS 15,FRANCE
关键词
D O I
10.1084/jem.178.4.1283
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We found that c-kit-positive, lineage marker-negative, Thy-1lo cells are present in both bone marrow and thymus (''BM c-kit'' and ''thymus c-kit, cells). Although the two cell types are phenotypically similar, only BM c-kit cells showed the potential to form colonies in vitro as well as in vivo. However, both of them revealed extensive growth and differentiation potential to T cells after direct transfer into an irradiated adult thymus, or a deoxyguanosine-treated fetal thymus. Time course analysis showed that thymus c-kit cells differentiated into CD4CD8 double-positive cells approximately 4 d earlier than BM c-kit cells did. In addition, anti-c-kit antibody blocked T cell generation of BM c-kit cells but not of thymus c-kit cells. intravenous injection of thymus c-kit resulted in the generation of not only T cells, but B as well as NK1.1+ cells. These data provide evidence that thymus c-kit cells represent common lymphoid progenitors with the differentiation potential to T, B, and possibly NK cells. The c-kit-mediated signaling appears to be essential in the transition from BM c-kit to thymus c-kit cells.
引用
收藏
页码:1283 / 1292
页数:10
相关论文
共 44 条
[1]   IDENTIFICATION IN ADULT BONE-MARROW OF PLURIPOTENT AND RESTRICTED STEM-CELLS OF MYELOID AND LYMPHOID SYSTEMS [J].
ABRAMSON, S ;
MILLER, RG ;
PHILLIPS, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1977, 145 (06) :1567-1579
[2]  
BOSWELL HS, 1984, J IMMUNOL, V133, P2940
[3]  
BRADLEY TR, 1979, BLOOD, V54, P1446
[4]  
Coffman R L, 1982, Immunol Rev, V69, P5
[5]   DIFFERENTIATION POTENTIAL OF SUBSETS OF CD4-8- THYMOCYTES [J].
CRISPE, IN ;
MOORE, MW ;
HUSMANN, LA ;
SMITH, L ;
BEVAN, MJ ;
SHIMONKEVITZ, RP .
NATURE, 1987, 329 (6137) :336-339
[6]   THYMUS RECONSTITUTION BY C-KIT-EXPRESSING HEMATOPOIETIC STEM-CELLS PURIFIED FROM ADULT-MOUSE BONE-MARROW [J].
DEVRIES, P ;
BRASEL, KA ;
MCKENNA, HJ ;
WILLIAMS, DE ;
WATSON, JD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 176 (06) :1503-1509
[7]   CHARACTERIZATION OF THE MURINE ANTIGENIC DETERMINANT, DESIGNATED L3T4A, RECOGNIZED BY MONOCLONAL-ANTIBODY GK1.5 - EXPRESSION OF L3T4A BY FUNCTIONAL T-CELL CLONES APPEARS TO CORRELATE PRIMARILY WITH CLASS II MHC ANTIGEN-REACTIVITY [J].
DIALYNAS, DP ;
WILDE, DB ;
MARRACK, P ;
PIERRES, A ;
WALL, KA ;
HAVRAN, W ;
OTTEN, G ;
LOKEN, MR ;
PIERRES, M ;
KAPPLER, J ;
FITCH, FW .
IMMUNOLOGICAL REVIEWS, 1983, 74 :29-56
[8]  
DORSHKIND K, 1985, J IMMUNOL, V134, P3798
[9]   L3T4 ANTIGEN EXPRESSION BY HEMATOPOIETIC PRECURSOR CELLS [J].
FREDRICKSON, GG ;
BASCH, RS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (04) :1473-1478
[10]  
GODFREY DI, 1992, J IMMUNOL, V149, P2281