iScience · 2025
Characterization of human CD34+ HSPC-derived neutrophils with limited myeloid-derived immunosuppressive cell activity.
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Webbers Steven D S, Gankema Angela A F, van Oosterom Fleur, Rojas-Rodriguez Felipe, Koops Dané S, Klaus Anna K, Geissler Judy, van Dam Teunis J P, Matlung Hanke L, van Bruggen Robin, Tercan Helin, Hoogendijk Arie J, Kuijpers Taco W
Аннотация
Neutrophils have limited utility as a fundamental research model and transfusion product due to their short lifespan. Here, we cultured CD34+ hematopoietic stem and progenitor cell (HSPC)-derived neutrophils and compared them to peripheral blood neutrophils in terms of morphology, phenotype, and function. Our culture system resulted in morphologically mature CD15+CD11b+CD16high neutrophils with effector functions almost indistinguishable from blood neutrophils, confirmed by a high similarity in transcription and protein abundance patterns. While exhibiting microbial killing capacity and antibody-dependent cellular cytotoxicity, these cells were deficient in myeloid-derived suppressor cell activity. This deficiency in immunosuppressive activity correlated with a distinct granular composition in comparison to blood neutrophils, instead of immunosuppressive characteristics that are currently held to define neutrophil-MDSC phenotype. Taken together, our cultured neutrophils closely resemble blood neutrophils, offering a repository for fundamental research and a step toward an effective transfusion product with limited immunosuppressive activity as a functional property.