Detection of tryptase-, chymase plus cells in human CD34+ bone marrow progenitors

被引:15
作者
Shimizu, Y
Suga, T
Maeno, T
Tsukagoshi, H
Kawata, T
Narita, T
Takahashi, T
Ishikawa, S
Morishita, Y
Nakajima, T
Hara, F
Miura, T
Kurabayashi, M
机构
[1] Gunma Univ, Grad Sch Med, Dept Med & Biol Sci, Gunma, Japan
[2] Gunma Univ, Grad Sch Med, Dept Med & Mol Sci, Gunma, Japan
[3] Inst Mol & Cellular Regulat, Mol Genet Lab, Gunma, Japan
[4] Gunma Univ, Grad Sch Med, Dept Thorac & Visceral Organ Surg, Gunma, Japan
[5] Gunma Univ, Grad Sch Med, Dept Tumor Pathol, Gunma, Japan
[6] Kirin Brewery Inc, Takasaki, Gumma, Japan
关键词
bone marrow; CD34; chymase; differentiation; human mast cells;
D O I
10.1111/j.1365-2222.2004.02105.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background Mast cells (MCs) arise from haematopoietic stem cells. We have recently reported that CD34(+) progenitors derived from human bone marrow (BM) develop into tryptase+, chymase+ MCs when cultured in the presence of recombinant human stem cell factor (rhSCF) and recombinant human IL-6 (rhIL-6). In an experiment for the expression of chymase during differentiation, chymase+ cells were detected in human BM, but tryptase+ cells were not found. Objective The purpose of this study was to show the appearance of chymase+ cells in CD34(+) cells with an origin different from MC differentiation. Methods CD34(+) cells from human BM were sorted with anti-CD117 monoclonal antibody (mAb), and cytospins of CD34(+), CD34(+)CD117(+), or CD34(+)CD117(-) were prepared. These cells were cultured with rhSCF+rhIL-6 for 12 weeks. Some of the cells were subjected to either histological stain with Wright-Giemsa or immunocytochemistry with anti-chymase mAb. Real-time RT-PCR was also performed to compare the transcriptional level of chymase from each cell preparation. Results Chymase was expressed in CD34(+) cells as well as human MCs by immunocytochemistry. Substantial CD34(+)CD117(-) cells, but not CD34(+)CD117(+) cells, were stained immunocytochemically with anti-chymase mAb. For 1 week culture with rhSCF+rhIL-6, no cells expressed chymase in any preparation. Real-time RT-PCR revealed positivity for chymase mRNA in CD34(+) cells, but it reduced at 1 week of culture, and increased as cells developed into MCs. Chymase mRNA in CD34(+)CD117(+) cells was negligible compared with that in CD34(+)CD117(-). Tryptase mRNA was below the detectable level in CD34(+) cells, and increased along with MC differentiation. After 12 weeks of culture, CD34(+)CD117(+) developed predominantly into MCs, whereas CD34(+)CD117(-) developed into monocytes/macrophages. Conclusion Our findings suggested that chymase is present not only in MCs but also in CD34(+)CD117(-) BM progenitors, but that its origin is different from the MC lineage.
引用
收藏
页码:1719 / 1724
页数:6
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