V. Rider et al., ESTROGEN AND PROGESTERONE CONTROL BASIC FIBROBLAST GROWTH-FACTOR MESSENGER-RNA IN THE RAT UTERUS, Journal of Endocrinology, 154(1), 1997, pp. 75-84
Cell proliferation and differentiation in the rodent uterus are probab
ly controlled by the interaction of female sex steroids with polypepti
de growth factors. Uterine basic fibroblast growth factor (bFGF) mRNA
was measured by RNase protection during the time (days 2-4) of endomet
rial cell proliferation in the pregnant rat. bFGF transcripts were det
ected at each of the 3 days of pregnancy examined. To investigate the
influence of oestrogen and progesterone on bFGF mRNA accumulation, ova
riectomized rats were treated with oestradiol for 48 h followed by a s
ingle injection of oestradiol, progesterone, the two steroids co-injec
ted or oil vehicle alone. Uterine RNA was collected 6 h after the last
hormone injection. Steroid treatments increased steady-state uterine
bFGF mRNA compared with vehicle control animals as measured by RNase p
rotection. Northern blot analysis of c-fos and c-jun mRNAs from these
same treatment soups revealed increased protooncogene expression in th
e uterus of hormone treated rats compared with the control animals. Te
mporal analysis of bFGF mRNA in ovariectomized rats at 1, 3 and 6 h af
ter acute oestrogen and oestrogen-progesterone co-administration showe
d a dual pattern of transcript accumulation. Both hormone treatments i
ncreased bFGF mRNA within 1 h compared with vehicle injected rats. Go-
administration of the two hormones, however, repressed bFGF mRNA accum
ulation relative to oestrogen at 3 and 6 h. Together, these studies pr
ovide evidence that bFGF control of uterine cell proliferation in preg
nant rats can occur from newly synthesized bFGF. Moreover, the results
suggest that progesterone is a potent stimulator of bFGF expression i
n the uterus.