ID | 30761 |
JaLCDOI | |
フルテキストURL | |
著者 |
Mizobuchi, Noriko
Kochi Municipal Central Hospital
Takahashi, Isao
Kochi Municipal Central Hospital
Horimi, Tadashi
Kochi Municipal Central Hospital
Yamamoto, Megumi
Kochi Municipal Central Hospital
Hamada, Kyoko
Kochi Municipal Central Hospital
Yorimitsu, Seiichi
Kochi Municipal Central Hospital
Kubonishi, Ichiro
Kochi Medical School
|
抄録 | 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. |
キーワード | isochromosome 17q
myeloid cell line
myelodysplastic syndrome
|
Amo Type | Article
|
出版物タイトル |
Acta Medica Okayama
|
発行日 | 1997-08
|
巻 | 51巻
|
号 | 4号
|
出版者 | Okayama University Medical School
|
開始ページ | 227
|
終了ページ | 232
|
ISSN | 0386-300X
|
NCID | AA00508441
|
資料タイプ |
学術雑誌論文
|
言語 |
英語
|
論文のバージョン | publisher
|
査読 |
有り
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PubMed ID | |
Web of Science KeyUT |