| Literature DB >> 34921959 |
Debra Van Egeren1, Baransel Kamaz2, Shichen Liu3, Maximilian Nguyen4, Christopher R Reilly5, Maria Kalyva6, Daniel J DeAngelo5, Ilene Galinsky5, Martha Wadleigh5, Eric S Winer5, Marlise R Luskin5, Richard M Stone5, Jacqueline S Garcia5, Gabriela S Hobbs7, Franziska Michor8, Isidro Cortes-Ciriano9, Ann Mullally10, Sahand Hormoz11.
Abstract
The JAK2-V617F mutation is the most common cause of myeloproliferative neoplasms. Although experiments have revealed that this gain-of-function mutation is associated with myeloid blood cell expansion and increased production of white cells, red cells, and platelets, the transcriptional consequences of the JAK2-V617F mutation in different cellular compartments of the bone marrow have not yet been fully elucidated. To study the direct effects of JAK2-V617F on bone marrow cells in patients with myeloproliferative neoplasms, we performed joint single-cell RNA sequencing and JAK2 genotyping on CD34+-enriched cells from eight patients with newly diagnosed essential thrombocythemia or polycythemia vera. We found that the JAK2-V617F mutation increases the expression of interferon-response genes (e.g., HLAs) and the leptin receptor in hematopoietic progenitor cells. Furthermore, we sequenced a population of CD34- bone marrow monocytes and found that the JAK2 mutation increased expression of intermediate monocyte genes and the fibrocyte-associated surface protein SLAMF7 in these cells.Entities:
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Year: 2021 PMID: 34921959 PMCID: PMC9332124 DOI: 10.1016/j.exphem.2021.12.364
Source DB: PubMed Journal: Exp Hematol ISSN: 0301-472X Impact factor: 3.249