Placental calcification commonly increases with gestational age. The mechan
ism of apatite mineralization probably involves one of three known mechanis
ms of tissue calcification: physiological (like bone), dt strophic (ischaem
ia-related) or metastatic (mineralization in a supersaturated environment).
This study was designed to determine the mechanism of calcification by exa
mining (1) the mineral content of placental calcifications in comparison to
other physiological and pathological apatites, and (2) the expression of b
one morphogenetic proteins (BMPs), which are important in physiological cal
cification, across gestational age. By energy-dispersive x-ray analysis (ED
XA), the Ca/P weight ratio for apatitic mineral from mature calcifications
was 2.00 +/- 0.05 (s.e.), which is similar to that for stones formed in a m
etastatic, supersaturated environment and lower than that observed in physi
ological calcification. Biologically active BMP, which was determined by bi
oassay, nas demonstrated in mature and postmature placentae. The BMPs PLAB,
PDF and related protein INSL-4 were identified by semiquantitative reverse
transcriptase polymerase chain reaction (RT-PCR), but their mRNA expressio
n was independent of gestational age (7-41 weeks of gestation). We conclude
that (1) the identified BMPs sere not related directly to placental calcif
ication, which argues against physiological calcification, and (2) the chem
ical composition of the apatitic mineral was suggestive of rapid formation
in a supersaturated environment, which is consistent with a metastatic mech
anism of calcification. (C) 2001 Harcourt Publishers Ltd.