Morphologic,cytochemical and neurochemical characterization of the human medulloblastoma cell line TE671 |
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Authors: | Paul M. Zeltzer Sandra L. Schneider Daniel D. Von Hoff |
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Affiliation: | (1) Department of Pediatrics, Division of Hematology/Oncology, University of Texas Health Science Center at San Antonio, 78284 San Antonio, TX, USA;(2) Department of Medicine, Division of Oncology, University of Texas Health Science Center at San Antonio, 78284 San Antonio, TX, USA;(3) Department of Pediatrics, The University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, 78284 San Antonio, TX, USA |
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Abstract: | Summary Medulloblastoma cell line TE671 was characterized by morphologic, cytochemical, neurochemical, and growth criteria. In contrast to the uniform, in vivo histopathologic appearance of the tumor, TE671 in vitro exhibits six morphologic subtypes (Types I–VI) in varying percentages over 14 days in culture. TE671 grows as a monolayer by the merging of separate foci. Cells were positive for Periodic acid Schiff (PAS) and reticulum, and negative for the glial marker, glial fibrillary acid protein (GFAP). Receptors for human Cab (EAC) were present on 19% of the cells. Neural associated isoenzymes, neuron specific enolase (NSE) and creatine kinase (CK-BB) were demonstrated in TE671. Progeny of a single clonogenic cell manifested the morphologic heterogeneity of cell types (I–VI). The absence of markers specific for glial cells suggests that TE671 is an early (less differentiated) precursor. TE671, the only continuous human medulloblastoma cell line, provides an experimental model with which to compare and identify the subpopulation of neoplastic cells in medulloblastoma ex vivo. |
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Keywords: | medulloblastoma clonogenicity complement enolase isoenzymes kinase |
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