کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4361309 | 1616212 | 2011 | 14 صفحه PDF | دانلود رایگان |
SummaryKaposi sarcoma (KS), an angioproliferative disease associated with Kaposi sarcoma herpesvirus (KSHV) infection, harbors a diversity of cell types ranging from endothelial to mesenchymal cells of unclear origin. We developed a three-dimensional cell model for KSHV infection and used it to demonstrate that KSHV induces transcriptional reprogramming of lymphatic endothelial cells to mesenchymal cells via endothelial-to-mesenchymal transition (EndMT). KSHV-induced EndMT was initiated by the viral proteins vFLIP and vGPCR through Notch pathway activation, leading to gain of membrane-type-1 matrix metalloproteinase (MT1-MMP)-dependent invasive properties and concomitant changes in viral gene expression. Mesenchymal markers and MT1-MMP were found codistributed with a KSHV marker in the same cells from primary KS biopsies. Our data explain the heterogeneity of cell types within KS lesions and suggest that KSHV-induced EndMT may contribute to KS development by giving rise to infected, invasive cells while providing the virus a permissive cellular microenvironment for efficient spread.
Graphical AbstractFigure optionsDownload high-quality image (291 K)Download as PowerPoint slideHighlights
► KSHV induces mesenchymal reprogramming of lymphatic endothelial cells (LECs) in 3D
► KSHV-activated Notch-MT1-MMP axis regulates LEC reprogramming
► KSHV-reprogrammed LECs are invasive
► 3D microenvironment of infected LECs leads to viral gene expression changes
Journal: - Volume 10, Issue 6, 15 December 2011, Pages 577–590