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Extramedullary tumor as presentation of leukemia: Establishment of a new human GPIIb- and GPIIIa-positive leukemia cell line
Authors:M. Yasunaga  R. Ryo  Y. Konaka  S. Sawada  H. Taniguchi  H. Sawada  M. Goto  J. Jikai  W. Sugano  K. Saigo  N. Yamaguchi
Affiliation:(1) Department of Laboratory Medicine, Kobe University School of Medicine, 7-5-1, Kusunoki-cho, Chuo-ku, 650 Kobe, Japan;(2) Blood Transfusion Service, Kobe University Hospital, Kobe, Japan;(3) Department of Medicine, Kitano Hospital, Osaka, Japan;(4) Department of Clinical Pathology, Kitano Hospital, Osaka, Japan;(5) First Department of Internal Medicine, Kansai Medical School, Osaka, Japan;(6) First Department of Internal Medicine, Kyoto University School of Medicine, Kyoto, Japan
Abstract:Summary A 25-year-old man noted swelling of the right cervical lymph nodes in October 1983. Diagnosis of malignant lymphoma was made on the basis of pathological examination of biopsies. Despite both chemotherapy and irradiation treatment, blast cells appeared in the peripheral blood and bone marrow in April 1984. Immunophenotypic analysis demonstrated that the blasts in the patient's peripheral blood expressed CD13, CD33, CD41a, and no markers for T or B lymphocytes, suggesting that he had been suffering from megakaryocytic sarcoma. We established a new cell line derived from the blasts in the peripheral blood, designated KH184. KH184 cells expressed glycoprotein (GP) Ib (CD42b) and GPIIb/IIIa (CD41a), while platelet peroxidase (PPO) activity was negative in an ultrastructural study. Both Northern blot and flow cytometric analysis of surface antigens and DNA content revealed that treatment with 12-O-tetradecanoylphorbol 13-acetate (TPA) did not induce the maturation of these cells. Various cytokines such as interleukin 3 (IL-3), interleukin 6 (IL-6), and leukemia inhibitory factor (LIF) had no effect in promoting the growth of KH184 cells. KH184 cells expressing CD41a seem to possess unusual characteristics. KH184 cells, human GPIIb- and GPIIIa-positive leukemia cells, which lack response to TPA-induced differentiaton, provide a new and unique model for the characterization of factors that are implicated in the terminal differentiation of megakaryocytes, and should aid in studies of the mechanism underlying the occurrence of megakaryocytic sarcoma.
Keywords:Extramedullary tumor  Malignant lymphoma  Granulocytic sarcoma  GPIIb- and GPIIIa-positive leukemia cell line
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