Connexins are considered to be involved in cell growth control, on the basis of studies mainly with tumorigenic cells. To study the role of connexin genes in normal cell growth control, we established fibroblast cell lines from connexin 43 (Cx43)-deficient mice and characterized their growth. Embryo
Growth and Differentiation of Osteoblast-Like Cells from Calvaria of Connexin43 Deficient Mice
β Scribed by M. Wiemann; B. Gramsch; E. Winterhager; K. Schirrmacher
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 264 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0933-5137
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β¦ Synopsis
Abstract
Extensive cellβcellβcoupling via gap junctions has been suspected to play an essential role for osteoblast development. Here, osteoblastβlike cells (OBL) from connexin(Cx)43 knock out mice were used to explore the role of Cx43 for osteoblast differentiation. Primary cultures of OBL were derived from calvaria of homozygous (Cx43β/β) and heterozygous (Cx43+/β) knock out mice and also from wild type controls (Cx43+/+). In Cx43β/β OBL Lucifer Yellow dye coupling was largely abolished demonstrating that small molecules could no longer be transferred among neighboring cells. Cx43β/β OBL grew out very slowly from calvarial fragments. Nevertheless their cell density around explants was increased 3βfold vs. controls after 3 weeks. Histochemistry showed that in many Cx43β/β OBL there was an increased alkaline phosphatase activity within the cytoplasm and close to the cell membrane. Mineralization was diminished in Cx43β/β cultures. In heterozygous Cx43+/β OBL all aforementioned effects were less pronounced, pointing to a geneβdosage effect. Data suggest that the loss of Cx43 indirectly impairs the osteoblastic phenotype, e.g. by disturbing cellular functions such as motility and/or secretion. If this holds true, all parameters in the interphase of enosseous implants which lower gap junction expression will also affect bone regeneration.
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