Differentiation of myeloid cells and 1,25-dihydroxyvitamin D3

被引:20
作者
Takahashi, T
Nakamura, K
Iho, S
机构
[1] Department of Immuno-Hematology, Kobe City General Hospital, Kobe
[2] College of Medical Technology, Kyoto University, Kyoto
[3] Dept. of Immunology and Parasitology, Fukui Medical School, Fukui
关键词
1,25(OH)(2)D-3; promyelocyte; differentiation; monocyte/macrophage myeloblast; CFU-GM; CFU-G; determinant gene of monocyte/macrophage differentiation;
D O I
10.3109/10428199709068268
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
It is well established that 1,25(OH)(2)D-3 induces monocyte/macrophage (Mo/M phi) colonies when added to culture of granulocyte/macrophage progenitors. Recently, we demonstrated that one of the target cells of 1,25(OH)(2)D-3 in Mo/M phi differentiation is the neutrophilic promyelocyte that is believed to belong to the neutrophilic lineage. This fact overthrows the established theory that normal hematopoietic precursors are committed to respective cell lineages and do not deviate from their own lineage. The lineage switching from the promyelocyte to Mo/M phi was suggested to be operating in vivo because 1,25(OH)(2)D-3 is a physiological substance produced by M phi. More recently, we have shown that transient exposure (24 h) of promyelocytes to 1,25(OH)(2)D-3 causes Mo/M phi differentiation. This strategy could be useful for examining the effects of 1,25(OH)(2)D-3 on the growth and differentiation of normal myeloblasts and myeloid progenitor cells. Recent advances in molecular biology have enabled investigators to identify a number of genes involved in Mo/M phi differentiation induced by 1,25(OH)(2)D-3. Some of these may be the determinant genes for Mo/M phi differentiation; however, further studies are required to determine the underlying mechanisms of Mo/M phi differentiation.
引用
收藏
页码:25 / &
页数:10
相关论文
共 59 条
[21]  
LARSSON LG, 1994, ONCOGENE, V9, P1247
[22]  
LASKY SR, 1990, CANCER RES, V50, P3087
[23]   THE ROLE OF THE HOMEOBOX GENE, HOX B7, IN HUMAN MYELOMONOCYTIC DIFFERENTIATION [J].
LILL, MC ;
FULLER, JF ;
HERZIG, R ;
CROOKS, GM ;
GASSON, JC .
BLOOD, 1995, 85 (03) :692-697
[24]   Transcriptional activation of the Cdk inhibitor p21 by vitamin D-3 leads to the induced differentiation of the myelomonocytic cell line U937 [J].
Liu, M ;
Lee, MH ;
Cohen, M ;
Bommakanti, M ;
Freedman, LP .
GENES & DEVELOPMENT, 1996, 10 (02) :142-153
[25]  
MARTIN M, 1993, J IMMUNOL, V150, P4395
[26]   THE EFFECT OF VITAMIN-D3 METABOLITES ON NORMAL AND LEUKEMIC BONE-MARROW CELLS-INVITRO [J].
MCCARTHY, D ;
HIBBIN, J ;
MIGUEL, JFS ;
FREAKE, H ;
RODRIGUES, B ;
ANDREWS, C ;
PINCHING, A ;
CATOVSKY, D ;
GOLDMAN, JM .
INTERNATIONAL JOURNAL OF CELL CLONING, 1984, 2 (04) :227-242
[27]   MOLECULAR-CLONING OF COMPLEMENTARY-DNA ENCODING THE AVIAN RECEPTOR FOR VITAMIN-D [J].
MCDONNELL, DP ;
MANGELSDORF, DJ ;
PIKE, JW ;
HAUSSLER, MR ;
OMALLEY, BW .
SCIENCE, 1987, 235 (4793) :1214-1217
[28]  
METCALF CD, 1977, BRIT J HAEMATOL, V37, P127
[29]   1-ALPHA,25-DIHYDROXYVITAMIN-D3 SUPPRESSES PROLIFERATION OF MURINE GRANULOCYTE-MACROPHAGE PROGENITOR CELLS (CFU-C) [J].
MIYAURA, C ;
ABE, E ;
NOMURA, H ;
NISHII, Y ;
SUDA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1982, 108 (04) :1728-1733
[30]   1-ALPHA, 25-DIHYDROXYVITAMIN-D3 INDUCES DIFFERENTIATION OF HUMAN MYELOID-LEUKEMIA CELLS [J].
MIYAURA, C ;
ABE, E ;
KURIBAYASHI, T ;
TANAKA, H ;
KONNO, K ;
NISHII, Y ;
SUDA, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1981, 102 (03) :937-943