Assuntos
Citometria de Fluxo/métodos , Cadeias Leves de Imunoglobulina/sangue , Mieloma Múltiplo/sangue , Neoplasia Residual/sangue , Espectrometria de Massas por Ionização por Electrospray/métodos , Medula Óssea/metabolismo , Medula Óssea/patologia , Cromatografia Líquida/métodos , Humanos , Imunoglobulina A/sangue , Imunoglobulina G/sangue , Quimioterapia de Indução/métodos , Quimioterapia de Manutenção/métodos , Espectrometria de Massas/métodos , Mieloma Múltiplo/tratamento farmacológico , Mieloma Múltiplo/patologia , Proteínas do Mieloma/análise , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz/métodosRESUMO
Three annotated CSF3R mRNA splice variants have been described. CSF3R-V1 is the wild-type receptor, while CSF3R-V4 is a truncated form increased in some patients with AML. CSF3R-V3 mRNA was identified in placenta more than 20 years ago, but remains largely uncharacterized due to the lack of a suitable detection assay. Using a novel digital PCR method to quantitate expression of each CSF3R mRNA splice variant in hematopoietic cells, CSF3R-V1 was most highly expressed followed by CSF3R-V3. Functional assays revealed expression of V3 alone conferred a hypoproliferative phenotype associated with defective JAK-STAT activation. However, coexpression of V1 with V3 rescued proliferative responses. Comparative analysis of V3/V1 expression in CD34+ cells from healthy donors and patients with AML revealed a statistically significant increase in the V3/V1 ratio only in the subset of patients with AML harboring SRSF2 mutations. Knockout of SRFS2 in KG-1 and normal CD34+ cells decreased the V3/V1 ratio. Collectively, these data are the first to demonstrate expression of the CSF3R-V3 splice variant in primary human myeloid cells and a role for SRSF2 in modulating CSF3R splicing. Our findings provide confirmatory evidence that CSF3R is a target of SRSF2 mutations, which has implications for novel treatment strategies for SRSF2-mutated myeloid malignancies.