Detection of placental growth hormone variant and chorionic somatomammotropin-L RNA expression in normal and diabetic pregnancy by reverse transcriptase-polymerase chain reaction
Lm. Hu et al., Detection of placental growth hormone variant and chorionic somatomammotropin-L RNA expression in normal and diabetic pregnancy by reverse transcriptase-polymerase chain reaction, MOL C ENDOC, 157(1-2), 1999, pp. 131-142
Diabetes is a common complication encountered during pregnancy. Earlier stu
dies indicated that diabetic placentas bear morphological alterations consi
stent with modified placental differentiation, including alterations in the
villous cellular content, structure, and total surface. Limited data assoc
iating the diabetic status with the expression of terminal placental differ
entiation markers are available. The human growth hormone/chorionic somatom
anamotropin (hGH/CS) family consists of five genes, one of which (GH-N) is
expressed efficiently in pituitary while the other four (CS-A, B, L, and hG
H-V) are expressed in placenta and represent ultimate placental differentia
tion markers. We developed and applied a sensitive RT-PCR method coupled wi
th diagnostic restriction digestion to determine the relative levels of the
hGH/CS family in normal pregnancies and examine whether their mRNA express
ion pattern is altered in pregnancies complicated by diabetes. We show that
relative hCS-L content changes during placental development. Specifically,
normal term placentas express higher relative levels of hCS-L, lower relat
ive hGH-V levels and a 70-fold lower hGH-V/CS-L mRNA ratio compared to earl
y placentas. Also, many term placentas from diabetic pregnancies express lo
wer relative levels of hCS-L mRNA and a much higher hGH-V/CS-L mRNA ratio c
ompared to normal term placenta, resembling more an early placenta pattern
of expression. Thus, our study suggests that the expression of terminal pla
cental differentiation markers, such as the hGH/CS genes, is altered in ter
m placentas from these diabetics reflecting either impaired placental diffe
rentiation or post-differentiation impairment of normal placental function.
(C) 1999 Elsevier Science Ireland Ltd. All rights reserved.