2005
DOI: 10.1038/emm.2005.6
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Leukotriene B4 pathway regulates the fate of the hematopoietic stem cells

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Cited by 37 publications
(20 citation statements)
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“…Activated metabolites of FFAs play vital roles in many cellular processes such as cell proliferation. Biologically active metabolites of FFAs act as second messengers to promote progenitor cell proliferation and to induce proliferation of human cord blood hematopoietic stem cells [22]. On the other hand, FFAs could decrease the proliferation of neuroblastoma cell [23].…”
Section: Discussionmentioning
confidence: 99%
“…Activated metabolites of FFAs play vital roles in many cellular processes such as cell proliferation. Biologically active metabolites of FFAs act as second messengers to promote progenitor cell proliferation and to induce proliferation of human cord blood hematopoietic stem cells [22]. On the other hand, FFAs could decrease the proliferation of neuroblastoma cell [23].…”
Section: Discussionmentioning
confidence: 99%
“…The resultant supernatants were assayed for protein and β-galactosidase activity. Luciferase activity was assayed in 10-μl samples of extract; the luciferase luminescence was counted in luminometer (Turner Design, TD-20/20) and normalized to the co-transfected β-galactosidase activity, as described elsewhere (Woo et al, 2000b;Chung et al, 2005;Shin et al, 2007). Transfection experiments were performed in triplicate with two independently isolated sets of cells, and the results were averaged.…”
Section: Transient Transfection and Nf-κb Luciferase Activity Assaymentioning
confidence: 99%
“…Further studies showed by in situ hybridisation that expression of BLT2 is significantly upregulated in a variety of human cancers (Yoo et al, 2004). In addition, it has been suggested that BLT2 is responsible for LTB 4 -induced generation of reactive oxygen species (ROS) through Rac/ERK and that this receptor is involved in cytokineinduced differentiation and expansion of haematopoietic stem cells (Woo et al, 2002;Chung et al, 2005). Stem cell factor and TNF-a are suggested to regulate BLT2 expression (Lundeen et al, 2006;Qiu et al, 2006).…”
mentioning
confidence: 99%