Characterization of progesterone receptor isoform expression in fetal membranes.

Abstract:

OBJECTIVE:To quantify expression of progesterone receptor (PR) messenger RNA (mRNA) isoforms in fetal membranes, and to determine whether these levels change in culture. STUDY DESIGN:Placentas from women undergoing term cesarean delivery before labor were collected. Layers of amnion, chorion, and decidua were separated manually, enzymatically digested, and separated further with the use of a density gradient. RNA was extracted immediately and after culture for 48 hours, then analyzed by quantitative reverse transcription polymerase chain reaction for PR-A, PR-B, and beta-2 microglobulin mRNA expression. Separation of cell types was confirmed by immunohistochemistry. RESULTS:PR isoform expression was identified in fetal membranes, with levels highest in decidua and below the limits of detection in amnion. The ratio of PR-A/PR-B mRNA was not significantly different between cell layers. PR mRNA isoform levels did not differ significantly in fresh versus cultured cells. CONCLUSION:Quantitative reverse transcription polymerase chain reaction was used to quantitate expression of PR mRNA isoforms in cells of fetal membranes and to validate systems for further study of PR with respect to inflammation, infection, and preterm delivery.

journal_name

Am J Obstet Gynecol

authors

Mills AA,Yonish B,Feng L,Schomberg DW,Heine RP,Murtha AP

doi

10.1016/j.ajog.2006.06.040

subject

Has Abstract

pub_date

2006-10-01 00:00:00

pages

998-1003

issue

4

eissn

0002-9378

issn

1097-6868

pii

S0002-9378(06)00764-2

journal_volume

195

pub_type

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