posted on 2019-11-14, 21:19authored byOphélie Gourgas, Gregory B. Cole, Lisa D. Muiznieks, Simon Sharpe, Marta Cerruti
Deposition of calcium phosphate minerals on the elastin-rich
medial
layers of arteries can cause severe cardiovascular complications.
There are no available treatments for medial calcification, and the
mechanism of mineral formation on elastin layers is still unknown.
We recently developed an in vitro model of medial calcification using
cross-linked elastin-like polypeptide (ELP) membranes immersed in
simulated body fluid (SBF). While mineral phase evolution matched
that observed in a mouse model of medial calcification, the long incubation
required was a practical limitation of this model. Using higher SBF
ion concentrations could be a solution to speed up mineral deposition,
but its effect on the mineralization process is still not well understood.
Here we analyze mineral formation and phase transformation on ELP
membranes immersed in high concentration SBF. We show that while mineral
deposition is significantly accelerated in these conditions, the chemistry
and morphology of the minerals deposited on the ELP membranes and
the overall mineralization process are strongly affected. Overall,
this work suggests that while the use of low concentration SBF in
this in vitro model is more appropriate to study medial calcification
associated with the loss of calcification inhibitors, higher SBF ion
concentration may be more relevant to study medial calcification in
patients with life-threatening diseases such as chronic kidney disease.