HIV-1 induction of CD40 on endothelial cells promotes the outgrowth of AIDS-associated B-cell lymphomas

被引:42
作者
Moses, AV
Williams, SE
Strussenberg, JG
Heneveld, ML
Ruhl, RA
Bakke, AC
Bagby, GC
Nelson, JA
机构
[1] OREGON HLTH SCI UNIV,DEPT MED,PORTLAND,OR 97201
[2] OREGON HLTH SCI UNIV,DEPT MOL & MED GENET,PORTLAND,OR 97201
[3] VET AFFAIRS MED CTR,PORTLAND,OR 97201
[4] OREGON HLTH SCI UNIV,DEPT PATHOL,PORTLAND,OR 97201
[5] OREGON HLTH SCI UNIV,DEPT MOL MICROBIOL & IMMUNOL,PORTLAND,OR 97201
关键词
D O I
10.1038/nm1197-1242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human immunodeficiency virus (HIV)-1 infection is associated with the development of aggressive extranodal B-cell non-Hodgkin's lymphomas. Using microvascular endothelial cell (MVEC)enriched bone marrow stromal cultures, HIV infection of stromal MVECs from lymphoma patients induced the outgrowth of malignant B cells. MVECs were the only HIV-infected cells in the stroma, and purified brain MVECs also induced a phenotype supportive of neoplastic B-cell attachment and proliferation. HIV infection of MVECs stimulated surface expression of CD40 and allowed preferential induction of the vascular cell adhesion molecule VCAM-1 after CD40 triggering. B-lymphoma cells expressed the CD40 ligand (CD40L), and blocking of CD40-CD40L interactions between HIV-infected MVECs and B-lymphoma cells inhibited B-cell attachment and proliferation. These observations suggest that HIV promotes B-lymphoma cell growth through facilitating attachment of lymphoma cells to HIV-infected MVECs and represent a novel mechanism through which viruses may induce malignancies.
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页码:1242 / 1249
页数:8
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