Olson G E, Winfrey V P, Matrisian P E, Melner M H, Hoffman L H
Department of Cell Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
J Endocrinol. 1997 Jan;152(1):69-80. doi: 10.1677/joe.0.1520069.
A glycoprotein, termed GP42, was previously identified in uterine fluid obtained from peri-implantation-stage rabbits. N-terminus amino acid sequencing of purified GP42 demonstrated identity through the first 13 amino acids with the beta subunit of liver haptoglobin. The present study was undertaken to determine if GP42 is indeed identical to haptoglobin and, if so, to determine whether it is expressed in the uterus as opposed to being present as a transudate from plasma. Reverse transcription-PCR amplification of poly(A)+ RNA prepared from implantation-stage rabbit endometrium with GP42- and haptoglobin-specific primers yielded a predicted 667 bp cDNA product. Sequence analysis of the cloned cDNA confirmed the identity of GP42 with beta-haptoglobin. Northern blot analysis demonstrated the specific expression of haptoglobin mRNA in the peri-implantation-stage endometrium and the absence of its expression in the estrous or day 4 pseudopregnant endometrium. Non-isotopic in situ hybridization revealed that the haptoglobin mRNA was restricted to the epithelium lining the luminal surface and mucosal folds of day 6(3/4) pregnant or pseudo-pregnant uteri and that no haptoglobin mRNA was detectable in the epithelium of the deep glands or cells of the stroma or myometrium. Similarly, in situ hybridization revealed no expression of haptoglobin mRNA in any cell types of the estrous uterus. These data establish the identity of GP42 with beta-haptoglobin and demonstrate that it is expressed in a stage-specific manner just prior to implantation, correlating with uterine receptivity to blastocyst implantation. Endometrial GP42 mRNA expression is not dependent on the presence of blastocysts.
一种名为GP42的糖蛋白,先前在植入前期兔子的子宫液中被鉴定出来。纯化后的GP42的N端氨基酸测序显示,其前13个氨基酸与肝结合珠蛋白的β亚基相同。本研究旨在确定GP42是否确实与结合珠蛋白相同,如果是,则确定它是在子宫中表达,还是作为血浆渗出物存在。用GP42和结合珠蛋白特异性引物对植入期兔子子宫内膜制备的poly(A)+ RNA进行逆转录-聚合酶链反应扩增,得到了一个预测的667 bp cDNA产物。对克隆的cDNA进行序列分析,证实了GP42与β-结合珠蛋白的同一性。Northern印迹分析表明,结合珠蛋白mRNA在植入前期子宫内膜中特异性表达,而在发情期或假孕第4天的子宫内膜中不表达。非同位素原位杂交显示,结合珠蛋白mRNA局限于妊娠或假孕第6(3/4)天子宫腔表面和黏膜皱襞的上皮细胞,在深部腺体上皮、基质或肌层细胞中未检测到结合珠蛋白mRNA。同样,原位杂交显示发情期子宫的任何细胞类型中都没有结合珠蛋白mRNA的表达。这些数据证实了GP42与β-结合珠蛋白的同一性,并表明它在植入前以阶段特异性方式表达,这与子宫对胚泡植入的接受性相关。子宫内膜GP42 mRNA的表达不依赖于胚泡的存在。