首页 | 本学科首页   官方微博 | 高级检索  
     


Growth factors derived from a human malignant glioma cell line,U-251MG
Authors:Jun-ichi Kuratsu  John E. Estes  Shumpei Yokota  M. Stephen Mahaley Jr.  G. Yancey Gillespie
Affiliation:(1) Department of Neurological Surgery, Kumamoto School of Medicine, Kumamoto University, Kumamoto, Japan;(2) Division of Neurological Surgery, University of Alabama at Birmingham, Birmingham, AL, USA;(3) Department of Microbiology and Immunology, University of North Carolina School of Medicine, Chapel Hill, NC, USA;(4) Division of Neurological Surgery, University of Alabama at Birmingham, Tinsley Harrison Tower, P.O. Box 65, 35294 Birmingham, AL, USA
Abstract:Summary A human malignant glioma cell line, U-251 Mg, cultured under serum free conditions, was shown to produce a growth factor for BALB/c 3T3 cells (glioma-derived growth factor-1, GDGF-1). The biological activity of GDGF-1 resided in a heat- and acid-resistant protein with a molecular weight (MW) of 25 kDa estimated by gel permeation chromatography. GDGF-1 activity was neutralized by a goat anti-human platelet derived growth factor (PDGF) antibody, indicating that the two factors were immunologically related. Furthermore, U-251 Mg cells constitutively expressed c-sis mRNA. When U-251 Mg cells were stimulated with bacterial lipopolysaccharide, 2 novel growth factors (GDGF-2 and GDGF-3) were produced in addition to the PDGF-like substance. GDGF-2 was determined to be >100 kDa MW and was not neutralized by the goat anti-PDGF antiserum. The biological activity of GDGF-3 was also heat- and acid- resistant with an apparent 14 kDa MW This factor also did not show any common antigenicity with PDGF. GDGF-2 and GDGF-3 are currently under investigation and evidence as to their natures will be published elsewhere. Our findings with this glioma cell line provide further evidence that inappropriate expression of growth factor-related genes could play important autocrine role(s) in the processes leading to malignant transformation and/or uncontrolled proliferation and may provide a paracrine stimulus for such processes as glioma neovascularization.
Keywords:glioma  growth factor  oncogene
本文献已被 SpringerLink 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号