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10.1182/bloodadvances.2017015073 http://scihub22266oqcxt.onion/10.1182/bloodadvances.2017015073 C5965045!5965045 !29776986     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=29776986 &cmd=llinks): Failed to open stream: HTTP request failed! 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The characteristics of vessel lining cells in normal spleens and their role in the pathobiology of myelofibrosis |pdf=|usr=}}{{29776986 }} gab.com Text The characteristics of vessel lining cells in normal spleens and their role in the pathobiology of myelofibrosis JO: Blood Adv http://www.kidney.de/pget.php?&tw=1&pmid=29776986 #FOAvip The CD34(-)CD8?(+), sinusoid lining, littoral cells (LCs), and CD34(+)CD8?(-), splenic vascular endothelial cells (SVECs) represent 2 distinct cellular types that line the vessels within normal spleens and those of patients with myelofibrosis (MF). To further understand the respective roles of LCs and SVECs, each was purified from normal and MF spleens, cultured, and characterized. Gene expression profiling indicated that LCs were a specialized type of SVEC. LCs possessed a distinct gene expression profile associated with cytoskeleton regulation, cellular interactions, endocytosis, and iron transport. LCs also were characterized by strong phagocytic activity, less robust tube-forming capacity and a limited proliferative potential. These characteristics underlie the role of LCs as cellular filters and scavengers. Although normal LCs and SVECs produced overlapping as well as distinct hematopoietic factors and adhesion molecules, the gene expression profile of MF LCs and SVECs distinguished them from their normal counterparts. MF SVECs were characterized by activated interferon signaling and cell cycle progression pathways and increased vascular endothelial growth factor receptor, angiopoietin-2, stem cell factor, interleukin (IL)-33, Notch ligands, and IL-15 transcripts. In contrast, the transcription profile of MF LCs was associated with mitochondrial dysfunction, reduced energy production, protein biosynthesis, and catabolism. Normal SVECs formed in vitro confluent cell layers that supported MF hematopoietic colony formation to a greater extent than normal colony formation. These data provide an explanation for the reduced density of LCs observed within MF spleens and indicate the role of SVECs in the development of extramedullary hematopoiesis in MF. Twit Text FOAVip The characteristics of vessel lining cells in normal spleens and their role in the pathobiology of myelofibrosis ????Blood Adv http://www.kidney.de/pget.php?&tw=1&pmid=29776986 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29776986 #FOAvip English Wikipedia <ref>{{Cite pmid|29776986 }}</ref> The characteristics of vessel lining cells in normal spleens and their role in the pathobiology of myelofibrosis #MMPMID29776986 Qiu J ; Salama ME ; Hu CS ; Li Y ; Wang X ; Hoffman R Blood Adv 2018[May]; 2 (10 ): 1130-1145 PMID29776986 show ga The CD34(-)CD8?(+), sinusoid lining, littoral cells (LCs), and CD34(+)CD8?(-), splenic vascular endothelial cells (SVECs) represent 2 distinct cellular types that line the vessels within normal spleens and those of patients with myelofibrosis (MF). To further understand the respective roles of LCs and SVECs, each was purified from normal and MF spleens, cultured, and characterized. Gene expression profiling indicated that LCs were a specialized type of SVEC. LCs possessed a distinct gene expression profile associated with cytoskeleton regulation, cellular interactions, endocytosis, and iron transport. LCs also were characterized by strong phagocytic activity, less robust tube-forming capacity and a limited proliferative potential. These characteristics underlie the role of LCs as cellular filters and scavengers. Although normal LCs and SVECs produced overlapping as well as distinct hematopoietic factors and adhesion molecules, the gene expression profile of MF LCs and SVECs distinguished them from their normal counterparts. MF SVECs were characterized by activated interferon signaling and cell cycle progression pathways and increased vascular endothelial growth factor receptor, angiopoietin-2, stem cell factor, interleukin (IL)-33, Notch ligands, and IL-15 transcripts. In contrast, the transcription profile of MF LCs was associated with mitochondrial dysfunction, reduced energy production, protein biosynthesis, and catabolism. Normal SVECs formed in vitro confluent cell layers that supported MF hematopoietic colony formation to a greater extent than normal colony formation. These data provide an explanation for the reduced density of LCs observed within MF spleens and indicate the role of SVECs in the development of extramedullary hematopoiesis in MF. |Flow Cytometry [MESH] |Humans [MESH] |Primary Myelofibrosis/*genetics/pathology [MESH]The characteristics of vessel lining cells in normal spleens and their(epmc).pdf DeepDyve Pubget Overpricing