Human cell line that differentiates to all myeloid lineages and expresses neutrophil secondary granule genes

被引:14
作者
Paul, CC
Aly, ES
Lehman, JA
Page, SM
Gomez-Cambronero, J
Ackerman, SJ
Baumann, MA
机构
[1] Dept Vet Affairs, Res Serv, Dayton, OH USA
[2] Wright State Univ, Dept Med, Dayton, OH 45435 USA
[3] Wright State Univ, Dept Physiol & Biophys, Dayton, OH 45435 USA
[4] Univ Illinois, Dept Biochem & Mol Biol, Chicago, IL USA
[5] Univ Illinois, Dept Med, Chicago, IL USA
关键词
cell line; differentiation; neutrophil; secondary granules; eosinophil;
D O I
10.1016/S0301-472X(00)00552-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The aim of this study was to characterize a human leukemic cell line that appears capable of spontaneous differentiation to all myeloid lineages. Materials and Methods. The MPD cell line was derived using standard tissue culture techniques from the peripheral blood of a patient with an aggressive nonchronic myelogenous leukemia myeloproliferative disorder. Immunophenotyping, cytogenetic analysis, reverse transcriptase polymerase chain reaction, Northern blotting, immunoblotting, and colony assays were used to characterize the line and to assess its ability to express lineage-specific genes representative of advanced differentiation. Results. Light microscopic morphologic analysis of the MPD cell line suggests that it has the unique property of spontaneous differentiation to mature-appearing neutrophils, macrophages, eosinophils, and basophils in proportions that approximate those found in normal bone marrow or peripheral blood. It was demonstrated that this cell line is capable of producing lineage-specific mRNA and granule proteins of at least two myeloid lineages, neutrophil and eosinophil, including neutrophil secondary granule proteins, which are not expressed in other available human cell lines. MPD cells were found to be capable of producing differentiated myeloid colonies (neutrophil, eosinophil, macrophge, mixed) in semisolid medium. Conclusion. The ability of MPD cells to express genetic programs associated with advanced differentiation of multiple myeloid lineages will make it a valuable tool for the study of the processes underlying lineage commitment and the regulation of expression of lineage-specific genes. (C) 2000 International Society for Experimental Hematology. Published by Elsevier Science Inc.
引用
收藏
页码:1373 / 1380
页数:8
相关论文
共 18 条
[1]   The Aml14 and Aml14.3D10 cell lines: A long-overdue model for the study of eosinophils and more [J].
Baumann, MA ;
Paul, CC .
STEM CELLS, 1998, 16 (01) :16-24
[2]   BIOSYNTHESIS OF GRANULE PROTEINS IN NORMAL HUMAN BONE-MARROW CELLS - GELATINASE IS A MARKER OF TERMINAL NEUTROPHIL DIFFERENTIATION [J].
BORREGAARD, N ;
SEHESTED, M ;
NIELSEN, BS ;
SENGELOV, H ;
KJELDSEN, L .
BLOOD, 1995, 85 (03) :812-817
[3]  
COLLINS SJ, 1987, BLOOD, V70, P1233
[4]   Cloning, expression, and characterization of the human eosinophil eotaxin receptor [J].
Daugherty, BL ;
Siciliano, SJ ;
DeMartino, JA ;
Malkowitz, L ;
Sirotina, A ;
Springer, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2349-2354
[5]  
FABIAN I, 1992, BLOOD, V80, P788
[6]  
FISCHKOFF SA, 1998, LEUKEMIA RES, V12, P679
[7]   HUMAN-LEUKEMIC MODELS OF MYELOMONOCYTIC DEVELOPMENT - A REVIEW OF THE HL-60 AND U937 CELL-LINES [J].
HARRIS, P ;
RALPH, P .
JOURNAL OF LEUKOCYTE BIOLOGY, 1985, 37 (04) :407-422
[8]   A new cytokine-dependent monoblastic cell line with t(9;11)(p22;q23) differentiates to macrophages with macrophage colony-stimulating factor (M-CSF) and to osteoclast-like cells with M-CSF and interleukin-4 [J].
Ikeda, T ;
Sasaki, K ;
Ikeda, K ;
Yamaoka, G ;
Kawanishi, K ;
Kawachi, Y ;
Uchida, T ;
Takahara, J ;
Irino, S .
BLOOD, 1998, 91 (12) :4543-4553
[9]  
JOHNSTON JJ, 1992, BLOOD, V79, P2998
[10]   S6 kinase p90(rsk) in granulocyte-macrophage colony-stimulating factor-stimulated proliferative and mature hematopoietic cells [J].
Joseph, DE ;
Paul, CC ;
Baumann, MA ;
GomezCambronero, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (22) :13088-13093