EXPRESSION AND LOCALIZATION OF MESSENGER-RNA FOR TUMOR-NECROSIS-FACTOR RECEPTOR (TNF-R)-I AND TNF-RII IN PREGNANT MOUSE UTERUS AND PLACENTA

被引:11
作者
ROBY, KF
LAHAM, N
KRONING, H
TERRANOVA, PF
HUNT, JS
机构
[1] UNIV KANSAS,MED CTR,DEPT ANAT & CELL BIOL,KANSAS CITY,KS 66160
[2] UNIV KANSAS,MED CTR,DEPT PHYSIOL,KANSAS CITY,KS 66160
[3] UNIV KANSAS,MED CTR,DEPT OBSTET & GYNECOL,KANSAS CITY,KS 66160
[4] UNIV KANSAS,MED CTR,DEPT PATHOL & ONCOL,KANSAS CITY,KS 66160
来源
ENDOCRINE | 1995年 / 3卷 / 08期
关键词
MESSENGER RNA; MOUSE; PLACENTA; TUMOR NECROSIS FACTOR; TUMOR NECROSIS FACTOR RECEPTORS; UTERUS;
D O I
10.1007/BF02953019
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The temporal and cell-specific localization of tumor necrosis factor (TNF) receptor mRNAs in the uterus and placenta during pregnancy in the mouse was investigated. Messenger RNA for TNF and the TNF receptors (TNF-RI, p55/p60 and TNF-RII, p75/p80) was assessed by northern blot and in situ hybridization. TNF, TNF-RI and TNF-RII specific transcripts were present on days 7 through 18 of pregnancy. Relative concentrations of TNF mRNA decreased from days 7 to 18 with levels being higher in the uterus than the placenta. In contrast TNF-RI mRNA levels were constant throughout gestation and no differences were seen between steady state levels in the uterus and placenta. Two transcripts for TNF-RII (3.6 and 4.5 kb) were identified in all tissues. Steady state levels of TNF-RII mRNA increased throughout gestation and levels were higher in the placenta than in the uterus. On day 9 of gestation, TNF-RI and TNF-RII mRNAs were localized to undecidualized endometrium, mesometrial decidual cells, and the developing placenta. In addition, muscle cells contained TNF-RI but not TNF-RII mRNA. By day 15 of gestation, TNF-RI and TNF-RII transcripts were primarily localized to the uterine epithelium and trophoblast giant cells and spongiotrophoblast cells in the placenta. The results of these studies reveal the uterine and placental cell-specific expression of TNF receptor mRNAs during pregnancy in the mouse and provide insight into the cellular targets of TNF action.
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页码:557 / 562
页数:6
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