Abstract:The present data indicate that under angiogenic stimulation macrophages develop an endothelial phenotype with expression of specific surface markers and even form cord- and tubular-like structures in vitro suggesting that this cell population may be recruited for vasculogenesis.
“…We also demonstrated that transplantation of both culture-expanded EPCs from MNCs and C6 glioma augmented neovascularization in experimental animals-bearing tumor, which was similar with other reports [26,27], though the culture condition of EPCs is different between our study and other’. We also found that previous studies all employed rat tail collagen fibronectin matrix as solid braces injected subcutaneously into the subject animals, but it was reported that Matrigel could induce cord formation from several non-endothelial cells including fibroblasts [28], baby murine kidney cells [29], aortic smooth muscle cells, murine leydig cells [30], and CD14 + monocytes seeded in Matrigel [31]. …”
BackgroundEPCs were isolated primarily in 1997 by Asahara et al. and recent studies indicated that bone-marrow-derived EPCs contributed little to the endothelium of tumor vessels. Tumors of the CNS system demonstrate various features of angiogenesis.MethodsEPCs derived from rat bone marrow were isolated and cultured in M199 medium without any induced factors. EPCs were studied using immunohistochemical staining, Flow cytometry and culture under three-dimensional condition to determine EPCs’ characteristics in vitro. We also established an animal model by injecting EPCs marked with Hoechst 33342 into the back of BALB/c nude mice and performed hematoxylin-eosin (HE) and immunofluorescent staining to study EPCs’ features in vivo. To research effect of EPCs on glioma, animals bearing tumors model with C6 glioma were established. About 27 day after injection, we performed immunohistochemical staining and Immunofluorescence staining.ResultsOur results showed that EPCs derived from rat bone marrow appeared typical morphological characteristics and were positive of CD34, CD133, KDR and CD31 antigens at different time in vitro under the special M199 medium without any induced factors. The percentage of cells that expressed CD133 decreased gradually. In brief, the present study showed that EPCs derived from rat bone marrow differentiated into ECs in medium the without any induced factors and formed tubular structures in three-dimensional circumstances. Animal experiments suggested that EPCs differentiated into ECs and other else non-endothelial cells, and that EPCs contributed M199 of glioma.DiscussionThese findings provides some novel results about biological characteristics of EPCs in vivo and ex vivo, and an update on the effect of EPCs on glioma and which would be helpful for the overall understanding of EPCs and make EPCs to be implied on the clinical therapy.
“…We also demonstrated that transplantation of both culture-expanded EPCs from MNCs and C6 glioma augmented neovascularization in experimental animals-bearing tumor, which was similar with other reports [26,27], though the culture condition of EPCs is different between our study and other’. We also found that previous studies all employed rat tail collagen fibronectin matrix as solid braces injected subcutaneously into the subject animals, but it was reported that Matrigel could induce cord formation from several non-endothelial cells including fibroblasts [28], baby murine kidney cells [29], aortic smooth muscle cells, murine leydig cells [30], and CD14 + monocytes seeded in Matrigel [31]. …”
BackgroundEPCs were isolated primarily in 1997 by Asahara et al. and recent studies indicated that bone-marrow-derived EPCs contributed little to the endothelium of tumor vessels. Tumors of the CNS system demonstrate various features of angiogenesis.MethodsEPCs derived from rat bone marrow were isolated and cultured in M199 medium without any induced factors. EPCs were studied using immunohistochemical staining, Flow cytometry and culture under three-dimensional condition to determine EPCs’ characteristics in vitro. We also established an animal model by injecting EPCs marked with Hoechst 33342 into the back of BALB/c nude mice and performed hematoxylin-eosin (HE) and immunofluorescent staining to study EPCs’ features in vivo. To research effect of EPCs on glioma, animals bearing tumors model with C6 glioma were established. About 27 day after injection, we performed immunohistochemical staining and Immunofluorescence staining.ResultsOur results showed that EPCs derived from rat bone marrow appeared typical morphological characteristics and were positive of CD34, CD133, KDR and CD31 antigens at different time in vitro under the special M199 medium without any induced factors. The percentage of cells that expressed CD133 decreased gradually. In brief, the present study showed that EPCs derived from rat bone marrow differentiated into ECs in medium the without any induced factors and formed tubular structures in three-dimensional circumstances. Animal experiments suggested that EPCs differentiated into ECs and other else non-endothelial cells, and that EPCs contributed M199 of glioma.DiscussionThese findings provides some novel results about biological characteristics of EPCs in vivo and ex vivo, and an update on the effect of EPCs on glioma and which would be helpful for the overall understanding of EPCs and make EPCs to be implied on the clinical therapy.
“…According to their initial discovery, EPCs were defined as cells positive for both hematopoietic stem cell markers such as CD34 and the endothelial marker protein KDR (Asahara et al 1997). However, increasing evidence suggests that myeloid cells can also give rise to endothelial cells (Rehman et al 2003;Gulati et al 2003;Romagnani et al 2005;Burger et al 2002;Fernandez Pujol et al 2000;Schmeisser et al 2001). Also, a recently identified population of peripheral blood-derived CD34 − CD133 + KDR + cells may differentiate into CD34 + CD133 + KDR + and eventually mature EC (Friedrich et al 2006).…”
Section: Determinants Of Circulating Cd14 + -Epcs Levelsmentioning
confidence: 99%
“…However, EPCs defined in this way represent a mixed population since it has become clear that at least two types of endothelial-lineage cells can be obtained from the in vitro culture of mononuclear cells (Rehman et al 2003;Hur et al 2004). Early EPCs, termed circulating angiogenic cells (CACs), are derived mainly from monocytic cells co-expressing some endothelial markers (Rehman et al 2003;Romagnani et al 2005;Fernandez Pujol et al 2000;Schmeisser et al 2001;Hur et al 2004). Early EPCs secrete large amounts of angiogenic growth factors (Rehman et al 2003;Hur et al 2004).…”
Section: Determinants Of Circulating Cd14 + -Epcs Levelsmentioning
confidence: 99%
“…Nevertheless, it has been convincingly demonstrated that EPCs bear various other cell surface markers, including markers of the monocytic cell lineage such as CD14 (Rehman et al 2003;Gulati et al 2003;Romagnani et al 2005;Burger et al 2002;Fernandez Pujol et al 2000;Schmeisser et al 2001). Importantly, both types of EPCs showed comparable vasculogenic capacity in vivo (Hur et al 2004).…”
There is evidence for two subpopulations among circulating endothelial progenitor cells (EPCs), i.e., CD34 + -EPCs and CD14 + -EPCs. Prior studies on the relationship between the level of EPCs and coronary artery disease (CAD), either did not distinguish between the two types of EPCs or studied only CD34 + -EPCs. We therefore investigated whether the number of circulating CD14 + -EPCs correlates with either CAD and/or cardiovascular risk factors. Circulating CD14 + -EPCs-as defined by the surface markers CD14 + KDR + -were analyzed by flow cytometry in 100 individuals [34 control subjects, 41 patients with stable CAD and 25 patients with acute coronary syndromes (ACS)]. The level of circulating CD14 + -EPCs was not significantly different in patients with normal coronary arteries compared to those with stable CAD or ACS. Neither was there any association between the severity of CAD or risk factors and the number of circulating CD14 + -EPCs. Thus, the number of circulating CD14 + -EPCs was not significantly correlated either with the severity of coronary disease or with cardiovascular risk factors.
“…They can develop an EC phenotype, especially when stimulated by VEGF and/or bFGF (Fernandez Pujol et al, 2000;Zhao et al, 2003), and produce a functional capillary-like mesh (Schmeisser et al, 2001) permeable by blood cells (Anghelina et al, 2004), hence recapitulating embryo vasculogenesis (Risau et al, 1988). Unlike these reports on the vascular ability by monocytes, mature macrophages have been found to form capillary-like lumina and branching patterns in vitro, confirming their propensity to participate to the de novo formation of microvessels (Anghelina et al, 2006b).…”
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