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10.1016/j.jip.2014.09.005 http://scihub22266oqcxt.onion/10.1016/j.jip.2014.09.005 C4252878!4252878 !25233872     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25233872 &cmd=llinks): Failed to open stream: HTTP request failed! 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Fucoidan stimulates cell division in the amebocyte-producing organ of the schistosome-transmitting snail Biomphalaria glabrata |pdf=|usr=}}{{25233872 }} gab.com Text Fucoidan stimulates cell division in the amebocyte-producing organ of the schistosome-transmitting snail Biomphalaria glabrata JO: J Invertebr Pathol http://www.kidney.de/pget.php?&tw=1&pmid=25233872 #FOAvip Adult Salvador (schistosome-resistant) strain Biomphalaria glabrata snails were injected with 5 ?l of 10 mg/ml solutions of the sulfated polysaccharides ? carageenan, dextran sulfate, fucoidan, and heparin, the nonsulfated polysaccharide laminarin, and the monosaccharides L-fucose and L-galactose, and mitotic activity in the amebocyte-producing organ (APO) was measured in histological sections at 24 h post injection. Among the substances tested, only fucoidan induced elevated mitotic activity. Desulfated fucoidan was not mitogenic, indicating that sulfate groups are required for activity. Schistosome-susceptible M-line snails possessed minimal or no hematopoietic tissue in their APO, which did not respond to fucoidan. Immersion of juvenile Salvador snails in 1 or 10 mg/ml solutions of fucoidan for 3 h did not elevate mitotic activity at 24 h post immersion, suggesting that the external and digestive tract epithelia of B. glabrata are impermeable to this molecule. These results provide support for the hypothesis that fucosylated glycans on the tegument and in excretory-secretory products of sporocysts of Schistosoma mansoni are in part responsible for increased mitotic activity in the APO of B. glabrata infected with this trematode or injected with its extracts. Twit Text FOAVip Fucoidan stimulates cell division in the amebocyte-producing organ of the schistosome-transmitting snail Biomphalaria glabrata ????J Invertebr Pathol http://www.kidney.de/pget.php?&tw=1&pmid=25233872 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25233872 #FOAvip English Wikipedia <ref>{{Cite pmid|25233872 }}</ref> Fucoidan stimulates cell division in the amebocyte-producing organ of the schistosome-transmitting snail Biomphalaria glabrata #MMPMID25233872 Sullivan JT ; Belloir JA ; Beltran RV ; Grivakis A ; Ransone KA J Invertebr Pathol 2014[Nov]; 123 (ä): 13-6 PMID25233872 show ga Adult Salvador (schistosome-resistant) strain Biomphalaria glabrata snails were injected with 5 ?l of 10 mg/ml solutions of the sulfated polysaccharides ? carageenan, dextran sulfate, fucoidan, and heparin, the nonsulfated polysaccharide laminarin, and the monosaccharides L-fucose and L-galactose, and mitotic activity in the amebocyte-producing organ (APO) was measured in histological sections at 24 h post injection. Among the substances tested, only fucoidan induced elevated mitotic activity. Desulfated fucoidan was not mitogenic, indicating that sulfate groups are required for activity. Schistosome-susceptible M-line snails possessed minimal or no hematopoietic tissue in their APO, which did not respond to fucoidan. Immersion of juvenile Salvador snails in 1 or 10 mg/ml solutions of fucoidan for 3 h did not elevate mitotic activity at 24 h post immersion, suggesting that the external and digestive tract epithelia of B. glabrata are impermeable to this molecule. These results provide support for the hypothesis that fucosylated glycans on the tegument and in excretory-secretory products of sporocysts of Schistosoma mansoni are in part responsible for increased mitotic activity in the APO of B. glabrata infected with this trematode or injected with its extracts. |Animals [MESH] |Biomphalaria/*drug effects [MESH] |Cell Division/*drug effects [MESH]Fucoidan stimulates cell division in the amebocyte-producing organ of (epmc).pdf DeepDyve Pubget Overpricing