Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2001-1-26
pubmed:abstractText
1. In this study, we investigated the biological effects of trimethyl (carboxymethyl) arsonium zwitterion, namely arsenobetaine (AsBe), which is a major organic arsenic compound in marine animals using murine bone marrow (BM) cells and compared them with those of an inorganic arsenical, sodium arsenite, in vitro. 2. Sodium arsenite showed strong cytotoxicity in BM cells, and its IC(50) was 6 microM. In contrast, AsBe significantly enhanced the viability of BM cells in a dose-dependent manner during a 72-h incubation; about a twofold increase in the viability of cells compared with that of control cells cultured with the medium alone was observed with a microM level of AsBe. 3. In morphological investigations, AsBe enhanced the numbers of large mature adherent cells, especially granulocytes, during a 72-h BM culture. When BM cells were cultured together with AsBe and a low dose (1 u ml(-1)) of recombinant murine granulocyte/macrophage colony-stimulating factor (rMu GM-CSF), significant additive-like increasing effects were observed on the numbers of both granulocytes and macrophages originated from BM cells. However, AsBe did not cause proliferation of BM cells at all as determined by colony-forming assay using a gelatinous medium. 4. These findings demonstrate the unique and potent biological effects in mammalian cells of AsBe, a major organic arsenic compound in various marine animals which are ingested daily as seafood in many countries.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0007-1188
pubmed:author
pubmed:issnType
Print
pubmed:volume
132
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
143-50
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:11156571-Animals, pubmed-meshheading:11156571-Arsenic, pubmed-meshheading:11156571-Arsenicals, pubmed-meshheading:11156571-Bone Marrow Cells, pubmed-meshheading:11156571-Cell Adhesion, pubmed-meshheading:11156571-Cell Count, pubmed-meshheading:11156571-Cell Survival, pubmed-meshheading:11156571-Cells, Cultured, pubmed-meshheading:11156571-Granulocyte-Macrophage Colony-Stimulating Factor, pubmed-meshheading:11156571-Granulocytes, pubmed-meshheading:11156571-Immunohistochemistry, pubmed-meshheading:11156571-Indicators and Reagents, pubmed-meshheading:11156571-Macrophages, pubmed-meshheading:11156571-Male, pubmed-meshheading:11156571-Mice, pubmed-meshheading:11156571-Mice, Inbred BALB C, pubmed-meshheading:11156571-Mice, Inbred DBA, pubmed-meshheading:11156571-Recombinant Proteins, pubmed-meshheading:11156571-T-Lymphocytes
pubmed:year
2001
pubmed:articleTitle
Modulation of cell adhesion and viability of cultured murine bone marrow cells by arsenobetaine, a major organic arsenic compound in marine animals.
pubmed:affiliation
Laboratory of Environmental Chemistry, School of Life Science, Tokyo University of Pharmacy and Life Science, Horinouchi 1432-1, Hachioji, Tokyo 192-0392, Japan. sakurai@ls.tokyo.ac.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't