Ge. Olson et al., SPECIFIC EXPRESSION OF HAPTOGLOBIN MESSENGER-RNA IN IMPLANTATION-STAGE RABBIT UTERINE EPITHELIUM, Journal of Endocrinology, 152(1), 1997, pp. 69-80
A glycoprotein, termed GP42, was previously identified in uterine flui
d obtained from peri-implantation-stage rabbits. N-terminus amino acid
sequencing of purified GP42 demonstrated identity through the first 1
3 amino acids with the beta subunit of liver haptoglobin. The present
study was undertaken to determine ii GP42 is indeed identical to hapto
globin and, if so, to determine whether it is expressed in the uterus
as opposed to being present as a transudate from plasma. Reverse trans
cription-PCR amplification of poly(A)(+) RNA prepared from implantatio
n-stage rabbit endometrium with GP42- and haptoglobin-specific primers
yielded a predicted 667 bp cDNA product. Sequence analysis of the clo
ned cDNA confirmed the identity of GP42 with beta-haptoglobin. Norther
n blot analysis demonstrated the specific expression of haptoglobin mR
NA in the peri-implantation-stage endometrium and the absence of its e
xpression in the estrous or day 4 pseudopregnant endometrium. Nonisoto
pic in situ hybridization revealed that the haptoglobin mRNA was restr
icted to the epithelium lining the luminal surface and mucosal folds o
f day 6 3/4 pregnant or pseudopregnant uteri and that no haptoglobin m
RNA was detectable in the epithelium of the deep glands or cells of th
e stroma or myometrium. Similarly, in situ hybridization revealed no e
xpression of haptoglobin mRNA in any cell types of the estrous uterus.
These data establish the identity of GP42 with beta-haptoglobin and d
emonstrate that it is expressed in a stage-specific manner just prior
to implantation, correlating with uterine receptivity to blastocyst im
plantation. Endometrial GP42 mRNA expression is not dependent on the p
resence of blastocysts.