The presence of MSA receptors on primary and passaged cells from multiple vascular sources suggests that receptors for insulin-like growth factors are an intrinsic component of the vascular endothelium.
Answers are grounded in this paper and cite their sources.
MSA receptors on cultured vascular cells support IGF signaling in endothelium; hypothesis-generating for vascular biology.
Endothelial cells were prepared from adult bovine pulmonary and systemic vessels and maintained as primary cultures, passaged cultures, and cloned cell strains. All cultures were shown to contain endothelial cells on the basis of several endothelial-specific and endothelial-associated traits. Both primary and passaged cells demonstrated specific receptors for the insulin-like growth factor, multiplication-stimulating activity (MSA). [125I]Iodo-MSA binding was greatest in cells derived from aortas, least in pulmonary venous cells, and intermediate in pulmonary arterial cells. When compared to MSA receptors on primary endothelial cell cultures derived from human umbilical veins or arteries, the bovine cells bound 4-10 times more MSA per cell. In all bovine cells, insulin competed weakly or not at all with [125I]iodo-MSA binding. The presence of MSA receptors on primary and passaged cells from five different vascular sources (three bovine and two human) suggests that receptors for the insulin-like growth factors may be an intrinsic component of the vascular endothelium.
No takes yet. Share an insight, caveat, or question.
Bar et al. (1982) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: