PDGFRA defines the mesenchymal stem cell Kaposi’s sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment
Autoři:
Julian Naipauer aff001; Santas Rosario aff001; Sachin Gupta aff001; Courtney Premer aff003; Omayra Méndez-Solís aff001; Mariana Schlesinger aff001; Virginia Ponzinibbio aff001; Vaibhav Jain aff004; Lauren Gay aff004; Rolf Renne aff004; Ho Lam Chan aff005; Lluis Morey aff005; Daria Salyakina aff001; Martin Abba aff002; Sion Williams aff002; Joshua M. Hare aff003; Pascal J. Goldschmidt-Clermont aff001; Enrique A. Mesri aff001
Působiště autorů:
Tumor Biology Program, Sylvester Comprehensive Cancer Center and Miami Center for AIDS Research, Department of Microbiology and Immunology, Miami, Florida, United States of America
aff001; UM-CFAR/ Sylvester CCC Argentina Consortium for Research and Training in Virally induced AIDS-Malignancies, Miami, Florida, United States of America
aff002; Interdisciplinary Stem Cell Institute; University of Miami Miller School of Medicine, Miami, Florida, United States of America
aff003; Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida, United States of America
aff004; Department of Human Genetics, Universidad Nacional de La Plata, La Plata, Argentina
aff005; Centro de Investigaciones Inmunológicas Básicas y Aplicadas, Facultad de Ciencias Médicas, Universidad Nacional de La Plata, La Plata, Argentina
aff006; Neurology Basic Science Division, Sylvester Comprehensive Cancer Center; University of Miami Miller School of Medicine, Miami, Florida, United States of America
aff007
Vyšlo v časopise:
PDGFRA defines the mesenchymal stem cell Kaposi’s sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment. PLoS Pathog 15(12): e32767. doi:10.1371/journal.ppat.1008221
Kategorie:
Research Article
doi:
https://doi.org/10.1371/journal.ppat.1008221
Souhrn
Kaposi’s sarcoma (KS) is an AIDS-defining cancer caused by the KS-associated herpesvirus (KSHV). Unanswered questions regarding KS are its cellular ontology and the conditions conducive to viral oncogenesis. We identify PDGFRA(+)/SCA-1(+) bone marrow-derived mesenchymal stem cells (Pα(+)S MSCs) as KS spindle-cell progenitors and found that pro-angiogenic environmental conditions typical of KS are critical for KSHV sarcomagenesis. This is because growth in KS-like conditions generates a de-repressed KSHV epigenome allowing oncogenic KSHV gene expression in infected Pα(+)S MSCs. Furthermore, these growth conditions allow KSHV-infected Pα(+)S MSCs to overcome KSHV-driven oncogene-induced senescence and cell cycle arrest via a PDGFRA-signaling mechanism; thus identifying PDGFRA not only as a phenotypic determinant for KS-progenitors but also as a critical enabler for viral oncogenesis.
Klíčová slova:
Carcinogenesis – Endothelial cells – Fluorescence imaging – Gene expression – Kaposi's sarcoma-associated herpesvirus – Mesenchymal stem cells – Kaposi sarcoma – Oncogenic signaling
Zdroje
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Štítky
Hygiena a epidemiologie Infekční lékařství LaboratořČlánek vyšel v časopise
PLOS Pathogens
2019 Číslo 12
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