Loss of myocardial capillary endothelial-cell alkaline phosphatase (ALP) activity in primary endothelial cell culture

Abstract

Primary cultures of rat myocardial capillary endothelial cells were established and characterized. A range of typical endothelial cell-specific markers were retained in vitro. Cell kinetic studies in confluent endothelial-cell cultures in vitro revealed a roughly 50-fold increase in the proportion of cells in s-phase, indicating a very considerable shortening of cell turnover time, compared to in vivo conditions. Alkaline phosphatase enzyme activity and encoding mRNA are strongly expressed in myocardial capillary endothelial cells in vivo, but were not detectable in vitro. This was true in cell cultures from two strains of rat, which revealed significantly different enzyme expression levels in vivo. In co-cultures of pericytes and endothelial cells, positive ALP enzyme reaction was detected in pericytes, which in vivo show only very weak enzyme reactivity. Treatment of cell cultures with </=10 M retinoic acid had no effect in pure endothelial cell cultures, but did increase ALP expression of pericytes in co-cultures. The observation of a loss of endothelial ALP expression in vitro supports other in vitro as well as our own in vivo observations, indicating a negative correlation of ALP expression and proliferative activity of endothelial cells.

Alkaline phosphatase-positive cells isolated from human hearts have mesenchymal stem cell characteristics

“…Here, we isolated cells by the explant cell culture technique, which may have favored the isolation of ALPL+ cells, and we used a medium described for the isolation of pericytes from human muscle tissue [18]. Cell culture enhances alkaline phosphatase expression in pericytes isolated from mammalian hearts [40]. We may therefore have favored the isolation of human heart pericytes, by selecting tissue nonspecific alkaline phosphatase-expressing cells from an explant cell culture.…”