TY - JOUR
T1 - New human myelodysplastic cell line, TER-3
T2 - G-CSF specific downregulation of Ca 2+/calmodulin-dependent protein kinase IV
AU - Mishima, Yuji
AU - Terui, Yasuhito
AU - Mishima, Yuko
AU - Katsuyama, Misa
AU - Mori, Masaki
AU - Tomizuka, Hiroshi
AU - Takizawa, Toshiyuki
AU - Miyazato, Akira
AU - Ueda, Masuzu
AU - Yamada, Muneo
AU - Hayasawa, Hirotoshi
AU - Mizunuma, Nobuyuki
AU - Ishizaka, Yukihito
AU - Ikeda, Kazuma
AU - Kato, Takashi
AU - Ozawa, Keiya
AU - Hatake, Kiyohiko
N1 - Funding Information:
This study was financed by a grant for clinical research from the Spanish Society of Cardiology, Instituto de Salud Carlos III – European Regional Development Fund (Cardiovascular Research Network RD12/0042; PI09/90506), AGAUR (2009 SGR 1195).
PY - 2002
Y1 - 2002
N2 - 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.
AB - 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.
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U2 - 10.1002/jcp.10095
DO - 10.1002/jcp.10095
M3 - Article
C2 - 12064461
AN - SCOPUS:18344390536
SN - 0021-9541
VL - 191
SP - 183
EP - 190
JO - Journal of Cellular Physiology
JF - Journal of Cellular Physiology
IS - 2
ER -