Generation of macrophages from early T progenitors in vitro

被引:50
作者
Lee, CK [1 ]
Kim, JK
Kim, Y
Lee, MK
Kim, K
Kang, JK
Hofmeister, R
Durum, SK
Han, SS
机构
[1] Chungbuk Natl Univ, Coll Pharm, Cheongju 361763, South Korea
[2] Chungbuk Natl Univ, Coll Vet Med, Cheongju 361763, South Korea
[3] Sahm Yook Univ, Dept Pharm, Seoul, South Korea
[4] NCI, Mol Immunoregulat Lab, Frederick, MD 21702 USA
关键词
D O I
10.4049/jimmunol.166.10.5964
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Early T progenitors in the thymus have been reported to have the capacity to develop into B cells, thymic dendritic cells, and NK cells. Here we describe conditions that induce early T progenitors to develop into macrophages. Initially, we observed that early T progenitors could be induced to develop into macrophages by cytokines produced from a thymic stromal cell line, TFGD, and later we found that the cytokine mixture of M-CSF plus IL-6 plus IL-7 also induced macrophage differentiation from pro-T cells. M-CSF by itself was unable to induce macrophage differentiation from early T progenitors. To correlate this observation with the developmental potential of early T progenitors, mouse embryonic thymocytes were sorted into four populations, pro-T1 to pro-T4, based on the expression of CD44 and CD25, and then cultured with TFGD culture supernatant. We found that pro-T1 and pro-T2 cells, but not pro-T3 and pro-T4 cells, generate macrophages. Limiting dilution analysis of the differentiation capability of sorted pro-T2 cells also confirmed that pro-T2 cells could generate macrophages. These results suggest that T cells and thymic macrophages could originate from a common intrathymic precursor.
引用
收藏
页码:5964 / 5969
页数:6
相关论文
共 32 条
[1]   Thymocyte selection: not by TCR alone [J].
Amsen, D ;
Kruisbeek, AM .
IMMUNOLOGICAL REVIEWS, 1998, 165 :209-229
[2]   THYMIC DENDRITIC CELLS AND T-CELLS DEVELOP SIMULTANEOUSLY IN THE THYMUS FROM A COMMON PRECURSOR POPULATION [J].
ARDAVIN, C ;
WU, L ;
LI, CL ;
SHORTMAN, K .
NATURE, 1993, 362 (6422) :761-763
[3]  
Björck P, 1998, J IMMUNOL, V161, P5795
[4]   SELECTIVE IMMORTALIZATION OF MURINE MACROPHAGES FROM FRESH BONE-MARROW BY A RAF/MYC RECOMBINANT MURINE RETROVIRUS [J].
BLASI, E ;
MATHIESON, BJ ;
VARESIO, L ;
CLEVELAND, JL ;
BORCHERT, PA ;
RAPP, UR .
NATURE, 1985, 318 (6047) :667-670
[5]   Defective T-cell receptor gamma gene rearrangement in interleukin-7 receptor knockout mice [J].
Candeias, S ;
Peschon, JJ ;
Muegge, K ;
Durum, SK .
IMMUNOLOGY LETTERS, 1997, 57 (1-3) :9-14
[6]   BIPOTENTIAL PRECURSORS OF B-CELLS AND MACROPHAGES IN MURINE FETAL LIVER [J].
CUMANO, A ;
PAIGE, CJ ;
ISCOVE, NN ;
BRADY, G .
NATURE, 1992, 356 (6370) :612-615
[7]   INTERLEUKIN-6 IS A PERMISSIVE FACTOR FOR MONOCYTIC COLONY FORMATION BY HUMAN HEMATOPOIETIC PROGENITOR CELLS [J].
JANSEN, JH ;
KLUINNELEMANS, JC ;
VANDAMME, J ;
WIENTJENS, GJHM ;
WILLEMZE, R ;
FIBBE, WE .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (04) :1151-1154
[8]   In vitro tracking of IL-7 responsiveness and gene expression during commitment of bipotent B-cell/macrophage progenitors [J].
Kee, BL ;
Paige, CJ .
CURRENT BIOLOGY, 1996, 6 (09) :1159-1169
[9]   Immunohistochemical and ultrastructural evidence for myelopoiesis in the scid/scid mouse thymus [J].
Kendall, MD ;
Lane, DP ;
Schumacher, U .
HISTOCHEMICAL JOURNAL, 1999, 31 (10) :651-660
[10]   Withdrawal of IL-7 induces Bax translocation from cytosol to mitochondria through a rise in intracellular pH [J].
Khaled, AR ;
Kim, K ;
Hofmeister, R ;
Muegge, K ;
Durum, SK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (25) :14476-14481