Kaposi's Sarcoma Cells: Long-Term Culture with Growth Factor from Retrovirus-Infected CD4$^{+}$ T Cells
Studies of the biology and pathogenesis of Kaposi's sarcoma (KS) have been hampered by the inability to maintain long-term cultures of KS cells in vitro. In this study AIDS-KS--derived cells with characteristic spindle-like morphology were cultured with a growth factor (or factors) released by...
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Published in | Science (American Association for the Advancement of Science) Vol. 242; no. 4877; pp. 426 - 430 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington, DC
The American Association for the Advancement of Science
21.10.1988
American Association for the Advancement of Science |
Subjects | |
Online Access | Get full text |
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Summary: | Studies of the biology and pathogenesis of Kaposi's sarcoma (KS) have been hampered by the inability to maintain long-term cultures of KS cells in vitro. In this study AIDS-KS--derived cells with characteristic spindle-like morphology were cultured with a growth factor (or factors) released by CD4$^{+}$ T lymphocytes infected with human T-lymphotropic virus type I or II (HTLV-I or HTLV-II) or with human immunodeficiency virus type 1 or 2 (HIV-1 or HIV-2). Medium conditioned by HTLV-II--infected, transformed lines of T cells (HTLV-II CM) contained large amounts of this growth activity and also supported the temporary growth of normal vascular endothelial cells, but not fibroblasts. Interleukin-1 and tumor necrosis factor--$\alpha $ stimulated the growth of the KS-derived cells, but the growth was only transient and these factors could be distinguished from that in HTLV-II CM. Other known endothelial cell growth promoting factors, such as acidic and basic fibroblast growth factors and epidermal growth factor, did not support the long-term growth of the AIDS-KS cells. The factor released by CD4$^{+}$ T cells infected with human retroviruses should prove useful in studies of the pathogenesis of KS. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0036-8075 1095-9203 |
DOI: | 10.1126/science.3262925 |