No abstract

The effect of chronic expression of flt3 ligand (FL) on in vivo hematopoiesis was studied. Retroviral vector-mediated gene transfer was used in a mouse model of bone marrow transplantation to enforce expression of mouse FL cDNA in hematopoietic tissues. As early as 2 weeks posttransplantation, peripheral blood white blood cell counts in FL-overexpressing recipients were significantly elevated compared with controls. With the exception of eosinophils, all nucleated cell lineages studied were similarly affected in these animals. Experimental animals also exhibited severe anemia and progressive loss of marrow-derived erythropoiesis. All of the FL-overexpressing animals, but none of the controls, died between 10 and 13 weeks posttransplantation. Upon histological examination, severe splenomegaly was noted, with progressive fibrosis and infiltration by abnormal lymphoreticular cells. Abnormal cell infiltration also occurred in other organ systems, including bone marrow and liver. In situ immunocytochemistry on liver sections showed that the cellular infiltrate was CD3+/NLDC145+/CD11c+, but B220− and F4/80−, suggestive of a mixed infiltrate of dendritic cells and activated T lymphocytes. Infiltration of splenic blood vessel perivascular spaces resulted in vascular compression and eventual occlusion, leading to splenic necrosis consistent with infarction. These results show that FL can affect both myeloid and lymphoid cell lineages in vivo and further demonstrate the potential toxicity of in vivo treatment with FL.

The effect of chronic expression of flt3 ligand (FL) on in vivowith progressive fibrosis and infiltration by abnormal lymphoreticular cells. Abnormal cell infiltration also occurred in hematopoiesis was studied. Retroviral vector-mediated gene transfer was used in a mouse model of bone marrow other organ systems, including bone marrow and liver. In situ immunocytochemistry on liver sections showed that the transplantation to enforce expression of mouse FL cDNA in hematopoietic tissues. As early as 2 weeks posttransplanta-cellular infiltrate was CD3 " /NLDC145 " /CD11c " , but B220 Ï and F4/80 Ï , suggestive of a mixed infiltrate of dendritic cells tion, peripheral blood white blood cell counts in FL-overexpressing recipients were significantly elevated compared and activated T lymphocytes. Infiltration of splenic blood vessel perivascular spaces resulted in vascular compression with controls. With the exception of eosinophils, all nucleated cell lineages studied were similarly affected in these and eventual occlusion, leading to splenic necrosis consistent with infarction. These results show that FL can affect animals. Experimental animals also exhibited severe anemia and progressive loss of marrow-derived erythropoiesis. All both myeloid and lymphoid cell lineages in vivo and further demonstrate the potential toxicity of in vivo treatment with of the FL-overexpressing animals, but none of the controls, died between 10 and 13 weeks posttransplantation. Upon FL. ᭧ 1997 by The American Society of Hematology. histological examination, severe splenomegaly was noted, 76