دورية أكاديمية

Tumor-derived interleukin-1α and leukemia inhibitory factor promote extramedullary hematopoiesis.

التفاصيل البيبلوغرافية
العنوان: Tumor-derived interleukin-1α and leukemia inhibitory factor promote extramedullary hematopoiesis.
المؤلفون: Barisas, Derek A. G.1,2,3 (AUTHOR), Kabir, Ashraf Ul1 (AUTHOR), Wu, Jun1 (AUTHOR), Krchma, Karen1 (AUTHOR), Kim, Minseo1 (AUTHOR), Subramanian, Madhav1 (AUTHOR), Zinselmeyer, Bernd H.1 (AUTHOR), Stewart, Colin L.4 (AUTHOR), Choi, Kyunghee1,2 (AUTHOR) kchoi@wustl.edu
المصدر: PLoS Biology. 5/3/2023, Vol. 21 Issue 5, p1-28. 28p. 1 Diagram, 6 Graphs.
مصطلحات موضوعية: *EXTRAMEDULLARY hematopoiesis, *LEUKEMIA inhibitory factor, *HEMATOPOIETIC stem cells, *COOPERATIVE binding (Biochemistry), *HEMATOPOIESIS, *MYELOID cells
مستخلص: Extramedullary hematopoiesis (EMH) expands hematopoietic capacity outside of the bone marrow in response to inflammatory conditions, including infections and cancer. Because of its inducible nature, EMH offers a unique opportunity to study the interaction between hematopoietic stem and progenitor cells (HSPCs) and their niche. In cancer patients, the spleen frequently serves as an EMH organ and provides myeloid cells that may worsen pathology. Here, we examined the relationship between HSPCs and their splenic niche in EMH in a mouse breast cancer model. We identify tumor produced IL-1α and leukemia inhibitory factor (LIF) acting on splenic HSPCs and splenic niche cells, respectively. IL-1α induced TNFα expression in splenic HSPCs, which then activated splenic niche activity, while LIF induced proliferation of splenic niche cells. IL-1α and LIF display cooperative effects in activating EMH and are both up-regulated in some human cancers. Together, these data expand avenues for developing niche-directed therapies and further exploring EMH accompanying inflammatory pathologies like cancer. This study shows that tumor-produced IL-1α and LIF promote extramedullary hematopoiesis. LIF directly expands splenic niche cells while IL-1α induces TNFα production in hematopoietic stem and progenitor cells to activate splenic niche cells; both expand myeloid-biased splenic hematopoiesis. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:15449173
DOI:10.1371/journal.pbio.3001746