The beta 1 integrin adhesion receptors mediate the binding of cells to
extracellular matrices, facilitating their growth, migration, and cap
acity to deposit matrix proteins: important factors in arterial resten
osis and atherosclerosis. The expression of integrins in human coronar
y artery is, however, unexplored. The aim of the current study was, th
erefore, to define the expression of beta 1 integrins by cultured huma
n coronary artery vascular smooth muscle cells (hCAVSMC) and in normal
human coronary artery; confirming whether or not this differs from th
e repertoire found in other species and human vessels. The expression
of beta 1 integrins by hCAVSMC was assessed by immuno-precipitation an
d the alkaline phosphatase anti-alkaline phosphatase (APAAP) immunoche
mical technique. In addition, mRNA expression was defined by reverse t
ranscription polymerase chain reaction (RT-PCR). Normal adult human co
ronary arteries (n = 4) were also stained by the APAAP method. In vitr
o hCAVSMC express alpha 2 beta 1 (a collagen and occasional laminin re
ceptor) and alpha 5 beta 1 (a fibronectin receptor) with lesser expres
sion of alpha 3 beta 1 (a multifunctional receptor). They do, however,
possess mRNA for several other integrins. Cells within the media of h
uman coronary artery wall express alpha 3 beta 1 and alpha 5 beta 1 bu
t not alpha 2 beta 1: instead the alternative collagen/laminin recepto
r, alpha 1 beta 1, is expressed in vivo. This pattern of expression di
ffers subtly from that described in rats though it closely parallels t
hat found in other human arteries.