| ID | 30761 |
| JaLCDOI | |
| FullText URL | |
| Author |
Mizobuchi, Noriko
Takahashi, Isao
Horimi, Tadashi
Yamamoto, Megumi
Hamada, Kyoko
Yorimitsu, Seiichi
Kubonishi, Ichiro
|
| Abstract | A new myeloid cell line, MTO-94, was established from the bone marrow of a patient with myelodysplastic syndrome (MDS). MTO-94 cells matured in culture medium without the addition of growth factors, and yielded neutrophils with pseudo-Pelger Huët anomaly or hypersegmentation until 6 months. Ten months after the start of cell cultivation, MTO-94 consisted of myeloblasts. Surface phenotypes were as follows: CD7 90.3%, CD13 99.6%, CD33 75.6%, HLA-DR 96.3% and CD34 0.9%. The karyotype was 46, XY, i(17q). The proliferation of MTO-94 cells was enhanced by rhlL-3, G-CSF, rhGM-CSF and rhSCF but not by rhlL-6 and erythropoietin. MTO-94 cells with i(17q) might be useful in the study of biological aspects of not only MDS, but also hematological malignancies with i(17q) as the sole chromosomal anomaly. |
| Keywords | isochromosome 17q
myeloid cell line
myelodysplastic syndrome
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| Amo Type | Article
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| Publication Title |
Acta Medica Okayama
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| Published Date | 1997-08
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| Volume | volume51
|
| Issue | issue4
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| Publisher | Okayama University Medical School
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| Start Page | 227
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| End Page | 232
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| ISSN | 0386-300X
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| NCID | AA00508441
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| Content Type |
Journal Article
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| language |
English
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| File Version | publisher
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| Refereed |
True
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| PubMed ID | |
| Web of Science KeyUT |