info:eu-repo/semantics/article
PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment
Fecha
2019-12-27Registro en:
Naipauer, Julian; Rosario, Santas; Gupta, Sachin; Premer, Courtney; Méndez Solís, Omayra; et al.; PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment; Public Library of Science; Plos Pathogens; 15; 12; 27-12-2019; 1-38
1553-7366
1553-7374
CONICET Digital
CONICET
Autor
Naipauer, Julian
Rosario, Santas
Gupta, Sachin
Premer, Courtney
Méndez Solís, Omayra
Schlesinger, Mariana
Ponzinibbio, Maria Virginia
Jain, Vaibhav
Gay, Lauren
Renne, Rolf
Chan, Ho Lam
Morey, Lluis
Salyakina, Daria
Abba, Martín Carlos
Williams, Sion
Hare, Joshua M.
Goldschmidt Clermont, Pascal
Mesri, Enrique Alfredo
Resumen
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.