The lymphatic cell environment promotes kaposi sarcoma development by prox1-enhanced productive lytic replication of kaposi sarcoma herpes virus

Dongwon Choi, Eunkyung Park, Kyu Eui Kim, Eunson Jung, Young Jin Seong, Luping Zhao, Shrimika Madhavan, George Daghlian, Hansuh H. Lee, Patill T. Daghlian, Saren Daghlian, Khoa Bui, Chester J. Koh, Alex K. Wong, Il Taeg Cho, Young Kwon Hong

Research output: Contribution to journalArticle

2 Scopus citations

Abstract

Kaposi sarcoma is the most common cancer in human immunodeficiency virus-positive individuals and is caused by Kaposi sarcoma-associated herpesvirus (KSHV). It is believed that a small number of latently infected Kaposi sarcoma tumor cells undergo spontaneous lytic reactivation to produce viral progeny for infection of new cells. Here, we use matched donor-derived human dermal blood and lymphatic endothelial cells (BEC and LEC, respectively) to show that KSHV-infected BECs progressively lose viral genome as they proliferate. In sharp contrast, KSHV-infected LECs predominantly entered lytic replication, underwent cell lysis, and released new virus. Continuous lytic cell lysis and de novo infection allowed LEC culture to remain infected for a prolonged time. Because of the strong propensity of LECs toward lytic replication, LECs maintained virus as a population, despite the death of individual host cells from lytic lysis. The master regulator of lymphatic development, Prox1, bound the promoter of the RTA gene to upregulate its expression and physically interacted with RTA protein to coregulate lytic genes. Thus, LECs may serve as a proficient viral reservoir that provides viral progeny for continuous de novo infection of tumor origin cells, and potentially BECs and mesenchymal stem cells, which give rise to Kaposi sarcoma tumors. Our study reveals drastically different host cell behaviors between BEC and LEC and defines the underlying mechanisms of the lymphatic cell environment supporting persistent infection in Kaposi sarcoma tumors.

Original languageEnglish (US)
Pages (from-to)3130-3144
Number of pages15
JournalCancer research
Volume80
Issue number15
DOIs
StatePublished - Aug 1 2020

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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