| Literature DB >> 12064461 |
Yuji Mishima1, Yasuhito Terui, Yuko Mishima, Misa Katsuyama, Masaki Mori, Hiroshi Tomizuka, Toshiyuki Takizawa, Akira Miyazato, Masuzu Ueda, Muneo Yamada, Hirotoshi Hayasawa, Nobuyuki Mizunuma, Yukihito Ishizaka, Kazuma Ikeda, Takashi Kato, Keiya Ozawa, Kiyohiko Hatake.
Abstract
We have established a new hematopoietic cell line from a patient with myelodysplastic syndrome (MDS), which was refractory anemia with excess blasts (RAEB). This cell line, designated TER-3, depends on several cytokines for long-term survival and growth, and requires interleukin-3 (IL-3) for continuous growth. Cytochemical analysis revealed that TER-3 cells are weakly dianisidine positive and nonspecific esterase positive, but peroxidase negative. The surface marker profile shows that the TER-3 cells are strongly positive for myeloid, lymphoid, and megakaryocytic antigens such as CD15, CD19, and CD61, and negative for some common multilineage antigens such as CD13, CD33, and CD34. Thus, this cell line has a multilineage phenotype, suggesting that the transformation event occurred in multipotent stem cells. Dianisidine- and nonspecific esterase-positive TER-3 cells increase with granulocyte-colony stimulating factor (G-CSF) rather than with IL-3. These results suggest that the cell line is useful for understanding the mechanism underlying G-CSF-associated hematopoietic cell differentiation and activation in the patient with MDS.Entities:
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Year: 2002 PMID: 12064461 DOI: 10.1002/jcp.10095
Source DB: PubMed Journal: J Cell Physiol ISSN: 0021-9541 Impact factor: 6.384