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Status |
Public on Dec 12, 2019 |
Title |
PDGFRA Defines the Mesenchymal Stem Cell Kaposi’s Sarcoma Progenitors by Enabling KSHV Oncogenesis in an Angiogenic Environment [ChIP-seq] |
Organism |
Mus musculus |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
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.
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Overall design |
We designed a novel model of “de novo” KSHV oncogenesis based on infection of PDGFRA-positive mesenchymal stem cell progenitors cultured in pro-angiogenic/vasculogenic KS-like growth conditions. This system serves as a unique and robust platform to identify KSHV oncogenic-pathways and their relationship with cellular lineages and extracellular growth environments. Additionally, it can further be exploited to genetically dissect and elucidate viral, host-cell and environmental features of KS pathobiology.
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Contributor(s) |
Mesri EA, Naipauer J, Chan HL |
Citation(s) |
31881074 |
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Submission date |
Dec 11, 2019 |
Last update date |
Feb 18, 2020 |
Contact name |
Martin Carlos Abba |
E-mail(s) |
mcabba@gmail.com
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Phone |
054-221-4236711
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Organization name |
School of Medical Sciences - UNLP
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Lab |
CINIBA
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Street address |
60 y 120
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City |
La Plata |
State/province |
Buenos Aires |
ZIP/Postal code |
1900 |
Country |
Argentina |
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Platforms (1) |
GPL19057 |
Illumina NextSeq 500 (Mus musculus) |
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Samples (16)
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GSM4214102 |
KSHV positive Pα(+)S MSCs in KS media H3K4me3 ChIP rep1 |
GSM4214103 |
KSHV positive Pα(+)S MSCs in KS media H3K4me3 ChIP rep2 |
GSM4214104 |
KSHV positive Pα(+)S MSCs in KS media H3K4me3 ChIP rep3 |
GSM4214105 |
KSHV positive Pα(+)S MSCs in KS media H3K27me3 ChIP rep1 |
GSM4214106 |
KSHV positive Pα(+)S MSCs in KS media H3K27me3 ChIP rep2 |
GSM4214107 |
KSHV positive Pα(+)S MSCs in KS media H3K27me3 ChIP rep3 |
GSM4214108 |
KSHV positive Pα(+)S MSCs in KS media IgG ChIP |
GSM4214109 |
KSHV positive Pα(+)S MSCs in KS media ChIP input |
GSM4214110 |
KSHV positive Pα(+)S MSCs in MEM alpha media H3K4me3 ChIP rep1 |
GSM4214111 |
KSHV positive Pα(+)S MSCs in MEM alpha media H3K4me3 ChIP rep2 |
GSM4214112 |
KSHV positive Pα(+)S MSCs in MEM alpha media H3K4me3 ChIP rep3 |
GSM4214113 |
KSHV positive Pα(+)S MSCs in MEM alpha media H3K27me3 ChIP rep1 |
GSM4214114 |
KSHV positive Pα(+)S MSCs in MEM alpha media H3K27me3 ChIP rep2 |
GSM4214115 |
KSHV positive Pα(+)S MSCs in MEM alpha media H3K27me3 ChIP rep3 |
GSM4214116 |
KSHV positive Pα(+)S MSCs in MEM alpha media IgG ChIP |
GSM4214117 |
KSHV positive Pα(+)S MSCs in MEM alpha media ChIP input |
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This SubSeries is part of SuperSeries: |
GSE141868 |
PDGFRA Defines the Mesenchymal Stem Cell Kaposi’s Sarcoma Progenitors by Enabling KSHV Oncogenesis in an Angiogenic Environment |
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Relations |
BioProject |
PRJNA594954 |
SRA |
SRP236882 |