Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-3
pubmed:dateCreated
2007-11-16
pubmed:abstractText
Membrane channel connexin (Cx) forms gap junctions that are implicated in the homeostatic regulation of multicellular systems; thus, hematopoietic cells were assumed not to express Cxs. However, hematopoietic progenitors organize a multicellular system during the primitive stage; thus, the aim of the present study was to determine whether Cx32, a member of the Cx family, may function during the primitive steady-state hematopoiesis in the bone marrow (BM). First, the numbers of mononuclear cells in the peripheral blood and various hematopoietic progenitor compartments in the BM decreased in Cx32-knockout (KO) mice. Second, on the contrary, the number of primitive hematopoietic progenitor cells, specifically the Lin(-)/c-kit(+)/Scal(+ )fraction, the KSL progenitor cell compartment, also increased in Cx32-KO mice. Third, expression of Cx32 was detected in Lin(-)/c-kit(+) hematopoietic progenitor cells of wild-type mice (0.27% in the BM), whereas it was not detected in unfractionated wild-type BM cells. Furthermore, cell-cycle analysis of the fractionated KSL compartment from Cx32-KO BM showed a higher ratio in the G(2)/M fraction. Taken together, all these results imply that Cx32 is expressed solely in the primitive stem cell compartment, which maintains the stemness of the cells, i.e., being quiescent and noncycling; and once Cx32 is knocked out, these progenitor cells are expected to enter the cell cycle, followed by proliferation and differentiation for maintaining the number of peripheral blood cells.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-2631
pubmed:author
pubmed:issnType
Print
pubmed:volume
217
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
105-13
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:17629738-Animals, pubmed-meshheading:17629738-Blotting, Western, pubmed-meshheading:17629738-Bone Marrow, pubmed-meshheading:17629738-Cell Differentiation, pubmed-meshheading:17629738-Cell Division, pubmed-meshheading:17629738-Cell Proliferation, pubmed-meshheading:17629738-Cells, Cultured, pubmed-meshheading:17629738-Connexins, pubmed-meshheading:17629738-Female, pubmed-meshheading:17629738-Flow Cytometry, pubmed-meshheading:17629738-G2 Phase, pubmed-meshheading:17629738-Hematopoietic Stem Cells, pubmed-meshheading:17629738-Ion Channels, pubmed-meshheading:17629738-Male, pubmed-meshheading:17629738-Mice, pubmed-meshheading:17629738-Mice, Inbred C57BL, pubmed-meshheading:17629738-Mice, Knockout, pubmed-meshheading:17629738-Nucleotidyltransferases, pubmed-meshheading:17629738-Proto-Oncogene Proteins c-kit
pubmed:year
2007
pubmed:articleTitle
Membrane channel connexin 32 maintains Lin(-)/c-kit(+) hematopoietic progenitor cell compartment: analysis of the cell cycle.
pubmed:affiliation
Division of Cellular and Molecular Toxicology, Center for Biological Safety and Research, National Institute of Health Sciences, Tokyo, Japan. yokohira@nihs.go.jp
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't