LABORATORY RESEARCH Induction of Multipotential Hematopoietic Progenitors from Human Pluripotent Stem Cells via Respecification of Lineage-Restricted Precursors Researchers report a strategy to respecify lineage-restricted CD34+CD45+ myeloid precursors derived from human pluripotent stem cells into multilineage progenitors that can be expanded in vitro and engrafted in vivo. [Cell Stem Cell] Abstract | Graphical Abstract RhoA GTPase Controls Cytokinesis and Programmed Necrosis of Hematopoietic Progenitors By using a RhoA conditional knockout mouse model, scientists showed that RhoA deficiency causes a multilineage hematopoietic failure that is associated with defective multipotent hematopoietic progenitor cells. [J Exp Med] Abstract TRIM28 Is Essential for Erythroblast Differentiation in the Mouse The authors tested the contribution of TRIM28 to globin gene regulation and erythropoiesis using a conditional loss of function in vivo model. They discovered that Trim28 genetic loss in the adult mouse leads to defective immature erythropoiesis in the bone marrow and consequently to anemia. [Blood] Abstract Osteoclasts Are Not Crucial for Hematopoietic Stem Cell Maintenance in Adult Mice Researchers transplanted hematopoietic stem cells from two osteopetrotic mouse models, with lack of osteoclasts or defective osteoclast function, to normal adult mice and examined the bone phenotype and hematopoiesis in the recipients. [Haematologica] Abstract | Full Article Cited2 Is Required for the Maintenance of Glycolytic Metabolism in Adult Hematopoietic Stem Cells Scientists showed that conditional deletion of Cited2 in murine hematopoietic stem cells results in elevated levels of reactive oxygen species, decreased cellular glutathione content, increased mitochondrial activity, and decreased glycolysis. [Stem Cell Dev] Abstract Adipocytic Cells Augment the Support of Primitive Hematopoietic Cells In Vitro, but Have No Effect in the Bone Marrow Niche under Homeostatic Conditions Researchers compared the ability of adipocytic and non-adipocytic cell lines to support primitive hematopoietic cells in vitro. Pre-adipocytic cell lines demonstrated enhanced support of hematopoietic cells. [Stem Cell Dev] Abstract Rapamycin Enhances Long-Term Hematopoietic Reconstitution of Ex Vivo Expanded Mouse Hematopoietic Stem Cells by Inhibiting Senescence A well-established ex vivo expansion system for mouse bone marrow hematopoietic stem cells (HSCs) was used to investigate whether inhibition of overactivated mammalian target of rapamycin with rapamycin can promote long-term hematopoiesis of ex vivo expanded HSCs and to elucidate the mechanisms of action of rapamycin. [Transplantation] Abstract Hematopoietic Stem Cell Expansion Caused by a Synthetic Fragment of Leptin Mice were treated with 1 mg/kg LEP5 for three days. The mature and primitive hematopoietic populations were quantified. Investigators observed that the mature populations from the bone marrow and spleen were not affected by LEP5. However, the peptide caused at least a two-fold increase in the number of hematopoietic stem cells, the most primitive population of the bone marrow. [Peptides] Abstract CLINICAL RESEARCH Efficacy of Deferred Dosing of Granulocyte Colony-Stimulating Factor in Autologous Hematopoietic Transplantation for Multiple Myeloma To determine whether delayed G-CSF dosage could result in equivalent ANC recovery and thereby improve cost effectiveness, researchers deferred the administration of G-CSF until WBC recovery had begun. There was no difference between groups in the incidence or duration of febrile neutropenia, duration of greater than or equal to grade III mucositis, weight gain, rash, engraftment syndrome or early death (100 days). [Bone Marrow Transpl] Full Article Outcome and Prognostic Factors for Patients Who Relapse after Allogeneic Stem Cell Transplantation Scientists studied 1080 patients that received hematopoietic stem cell transplantation between 2004 and 2008, among whom 351 relapsed. The 3-year post-relapse overall survival was 19%. Risk factors for mortality after relapse included shorter time to relapse, higher disease risk index at hematopoietic stem cell transplantation, myeloablative conditioning, high pre-transplantation co-morbidity index, and graft-versus-host disease occurring prior to relapse. [Biol Blood Marrow Transpl] Abstract  |