This article dedicated to Ines Mandl at her 80th birthday is a short review
of the recent work of our team on the elastin receptor. Our studies starte
d in the early nineteen eighties aimed at the understanding of cell-elastin
interactions, The first experiments reviewed demonstrated the inducible in
teraction of cells - smooth muscle cells, fibroblasts - with elastic fibers
, Their strong adhesion was accelerated and amplified by elastin peptides a
nd cell adhesion to elastin needed protein neosynthesis. The demonstration
of the presence of the elastin receptor on leukocytes facilitated the detai
led description of the transmission pathway from receptor to the intracellu
lar sites activated by the receptor: modifications of ion fluxes, increase
of elastase production and excretion of reactive oxygen species, superoxide
and NO., The calcium transients triggered by elastin peptides acting on th
e receptor decrease with age, the receptor appears to be uncoupled from the
G-proteins, but superoxide release is increased. As circulating blood was
shown to contain elastin peptides at concentrations saturating for the rece
ptor (mu g/ml conc-s for a Kd in the nanomolar range), the receptor on cell
s in contact with excess agonists is constantly overstimulated, The continu
ous release of lytic enzymes and free radicals might well be involved in ce
ll damage. This was demonstrated with human lymphocytes undergoing cell dea
th by necrosis and apoptosis in presence of higher concentrations of elasti
n peptides.