Vasculogenesis: A process of vessel formation and its role during Ewing's sarcoma development

Vasculogenesis is the process by which Endothelial Precursor Cells (EPCs) form a vasculature. This process has been traditionally regarded as an embryological process of vessel formation. However, as early as in the 60's the concept of postnatal vasculogenesis was introduced, with a strong resurface of this idea in recent years. Similarly, previous work on a mouse skin tumor model provided us with the grounds to consider the role of vasculogenesis during tumor formation. ^ We examined the contribution of donor bone marrow (BM)-derived cells to neovascularization in recipient nude mice with Ewing's sarcoma. Ewing's sarcoma is a primitive neuroectodermal tumor that most often affects children and young adults between 5 and 30 years of age. Despite multiple attempts to improve the efficacy of chemotherapy for the disease, the 2-year metastases-free survival rate for patients with Ewing's sarcoma has not improved over the past 15 years. New therapeutic approaches are therefore needed to reduce the mortality rate. ^ The contribution of BM endothelial precursor cells in the development of Ewing's sarcoma was examined using different strategies to track the donor-derived cells. Using a BMT model that takes advantage of MHC differences between donor and recipient mice, we have found that donor BM cells were involved in the formation of Ewing's sarcoma vasculature. ^ Cells responsible for this vasculogenesis activity may be located within the stem cell population of the murine BM. These stem cells would not only generate the hematopoietic lineage but they would also generate ECs. Bone marrow SP (Side Population) cells pertain to a subpopulation that can be identified using flow cytometric analysis of Hoechst 33342-stained BM. This population of cells has HSC activity. We have tested the ability of BM SP cells to contribute to vasculogenesis in Ewing's sarcoma using our MHC mismatched transplant model. Mice transplanted with SP cells developed tumor neovessels that were derived from the donor SP cells. Thus, SP cells not only replenished the hematopoietic system of the lethally irradiated mice, but also differentiated into a non-hematopoietic cell lineage and contributed to the formation of the tumor vasculature. ^ In summary, we have demonstrated that BM-derived cells are involved in the generation of the new vasculature during the growth of Ewing's sarcoma. The finding that vasculogenesis plays a role in Ewing's sarcoma development opens the possibility of using genetically modified BM-derived cells for the treatment of Ewing's sarcomas. ^

Data Compilation of the Research Vessel METEOR (1964)

In 2008, the 50th anniversary of the IGY (International Geophysical Year), WDCMARE presents with this CD publication 3632 data sets in Open Access as part of the most important results from 73 cruises of the research vessel METEOR between 1964 and 1985. The archive is a coherent organized collection of published and unpublished data sets produced by scientists of all marine research disciplines who participated in Meteor expeditions, measured environmental parameters during cruises and investigated sample material post cruise in the labs of the participating institutions. In most cases, the data was gathered from the Meteor Forschungsergebnisse, published by the Deutsche Forschungsgemeinschaft (DFG). A second important data source are time series and radiosonde ascensions of more than 20 years of ships weather observations, which were provided by the Deutscher Wetterdienst, Hamburg. The final inclusion of all data into the PANGAEA information system ensures secure archiving, future updates, widespread distribution in electronic, machine-readable form with longterm access via the Internet. To produce this publication, all data sets with metadata were extracted from PANGAEA and organized in a directory structure on a CD together with a search capability.