KSHV infection of endothelial precursor cells with lymphatic characteristics as a novel model for translational Kaposi's sarcoma studies

• Published in: PLoS pathogens 2023-01, Vol.19 (1), p.e1010753-e1010753
• Main Authors: Tuohinto, Krista, DiMaio, Terri A, Kiss, Elina A, Laakkonen, Pirjo, Saharinen, Pipsa, Karnezis, Tara, Lagunoff, Michael, Ojala, Päivi M
• Format: Article
• Language: English
• Subjects: Analysis; Animals; Biology and Life Sciences; Blood; Blood circulation; Care and treatment; Causes of; Cell culture; Cells; Colonies; Copy number; Cytology; Development and progression; Disease susceptibility; Endothelial Cells; Endothelium; Endothelium, Vascular - pathology; Gene expression; Genomes; Genomics; Health aspects; Herpes viruses; Herpesvirus 8, Human - genetics; Hyperplasia; In vivo methods and tests; Infections; Kaposi's sarcoma; Kaposis sarcoma; Medical research; Medicine and Health Sciences; Medicine, Experimental; Mice; Phenotypes; Precursors; Sarcoma; Sarcoma, Kaposi; Translation; Translational research; Tumor cells; Viruses
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1010753

Kaposi's sarcoma herpesvirus (KSHV) is the etiologic agent of Kaposi's sarcoma (KS), a hyperplasia consisting of enlarged malformed vasculature and spindle-shaped cells, the main proliferative component of KS. While spindle cells express markers of lymphatic and blood endothelium, the origin of spindle cells is unknown. Endothelial precursor cells have been proposed as the source of spindle cells. We previously identified two types of circulating endothelial colony forming cells (ECFCs), ones that expressed markers of blood endothelium and ones that expressed markers of lymphatic endothelium. Here we examined both blood and lymphatic ECFCs infected with KSHV. Lymphatic ECFCs are significantly more susceptible to KSHV infection than the blood ECFCs and maintain the viral episomes during passage in culture while the blood ECFCs lose the viral episome. Only the KSHV-infected lymphatic ECFCs (K-ECFCLY) grew to small multicellular colonies in soft agar whereas the infected blood ECFCs and all uninfected ECFCs failed to proliferate. The K-ECFCLYs express high levels of SOX18, which supported the maintenance of high copy number of KSHV genomes. When implanted subcutaneously into NSG mice, the K-ECFCLYs persisted in vivo and recapitulated the phenotype of KS tumor cells with high number of viral genome copies and spindling morphology. These spindle cell hallmarks were significantly reduced when mice were treated with SOX18 inhibitor, SM4. These data suggest that KSHV-infected lymphatic ECFCs can be utilized as a KSHV infection model for in vivo translational studies to test novel inhibitors representing potential treatment modalities for KS.