Shedding of cytoplasm from circulating megakaryocytes (MKs) within the
pulmonary vasculature suggests the lungs are an important site for no
rmal platelet production. Fetal lungs receive only a minor fraction of
the circulating blood volume. The placenta may act as a site for intr
auterine platelet formation. Isolation of MKs from fetal vessels withi
n the placenta has not been previously reported. Immediately after del
ivery, 3 human placentae were subjected to forward and retrograde perf
usion across the placental capillary bed on the fetal side. MKs in per
fusates were harvested by 'whole blood filtration' and identified by m
orphological and immunochemical methods. All perfusates yielded MKs. Q
ualitatively MKs with copious cytoplasm were more commonly found in pe
rfusates collected from fetal arteries compared with those from fetal
veins. This is consistent with filtration of MKs and fragmentation of
their cytoplasm within the placental microcirculation to produce plate
lets. Perfusion of human placentae followed by filtration of perfusate
s is a useful technique for harvesting fetal MKs and permitting furthe
r elucidation of their physiological role.