T. Jansson et al., CELLULAR-LOCALIZATION OF GLUCOSE-TRANSPORTER MESSENGER-RNA IN HUMAN PLACENTA, Reproduction, fertility and development, 7(6), 1996, pp. 1425-1430
High levels of expression of the glucose transporter (GLUT) isoforms 1
and 3 have been demonstrated in the human placenta by Northern blotti
ng. However, the cellular localization of placental GLUT mRNA has not
been described. Furthermore, recent preliminary kinetic data indicate
that GLUT 2 might be present in syncytiotrophoblast. Human placental t
issue from preterm (16-22 weeks) and term pregnancies was collected fo
r identification and localization of glucose transporter mRNA. Followi
ng paraffin embedding, sections were cut and in situ hybridization was
performed with fluorescein-labelled cRNA. In addition, immunoblotting
and immunocytochemistry were carried out using an anti-GLUT 2 antibod
y. GLUT 1 mRNA was highly expressed in syncytiotrophoblast cells at te
rm. GLUT 1 expression was much less abundant in non-syncytial cells. I
n contrast, GLUT 3 mRNA was present in lower amounts and more evenly d
istributed between syncytial and other placental cells. GLUT 1 mRNA wa
s also highly abundant in preterm syncytiotrophoblast. The cellular di
stributions of GLUT 1 and GLUT 3 mRNA in the preterm placentas were si
milar to those in term tissue. With regard to GLUT 1, these findings c
orrelate well with cellular localization and gestational development o
f GLUT 1 protein. No GLUT 2 protein was detected. It is concluded that
GLUT 1 is the main isoform involved in transplacental glucose transpo
rt in the human.