THE ACTION OF THE SYNTHETIC POLYPEPTIDE VALYL-OXYTOCIN ON THE HUMAN UTERUS IN VITRO AND IN VIVO

1959 ◽  
Vol XXXII (III) ◽  
pp. 391-398 ◽  
Author(s):  
B. Berde ◽  
K. Saameli
1973 ◽  
Vol 74 (4) ◽  
pp. 756-768 ◽  
Author(s):  
A. R. Krishnan ◽  
V. Hingorani ◽  
K. R. Laumas

ABSTRACT The in vivo and in vitro binding of 3H-oestradiol-17β to cytoplasmic and nuclear fractions of the human endometrium and myometrium was demonstrated by different techniques. Sucrose density gradient ultracentrifugation of the endometrial cytoplasm showed that oestradiol binds with two specific proteins sedimenting at 8.5 S and 5.1 S. Myometrial cytoplasmic oestrogen binding protein (OeBP) had a sedimentation coefficient of 5.1 S. Nuclear OeBP in the endometrium and myometrium had the same sedimentation value of 4.2 S. The endometrial cytoplasmic OeBP separated by gel chromatography showed association with both oestradiol and oestrone in the ratio of 2:1. The OeBP in nuclear fraction of the endometrium and myometrium showed binding with oestradiol and oestrone in the ratio of 2.5:1 and 2:1 respectively. The association of oestrone along with oestradiol with receptors of the endometrial and myometrial nuclear and cytoplasmic fractions suggests that oestrone may play a significant role in the overall action of oestrogens in the human uterus. Studies on ligand specificity of the OeBPs showed that oestrone which is a comparatively weaker oestrogen, competitively displaced bound 3H-oestradiol, more or less in a similar way as a highly potent oestrogen diethylstilboestrol (DOeS). Chlormadinone acetate (CAP), among the progestational steroids tested, maximally displaced bound oestradiol. The significance of these findings in the mechanism of action of oestradiol in the human uterus is discussed.


1959 ◽  
Vol 19 (2) ◽  
pp. 150-157 ◽  
Author(s):  
V. R. PICKLES

SUMMARY The guinea-pig uterus and strips of human myometrium are stimulated in vitro by ether extracts of menstrual fluid; the guinea-pig uterus is also stimulated in vivo by intravenous or intracardiac injections of the same extracts. The amount of the active material recovered from menstrual fluid probably varies from subject to subject, and in one instance was shown to decrease steadily from the beginning to the end of the menstrual period. The uterine responses in vitro take several forms, all excitatory; they are compared with the contractions of the human uterus in vivo during normal menstruation and dysmenorrhoea.


2010 ◽  
Vol 22 (9) ◽  
pp. 52
Author(s):  
L. Ye ◽  
R. Mayberry ◽  
E. Stanley ◽  
A. Elefanty ◽  
C. Gargett

The human uterus develops from the distal Mullerian Duct, a derivative of the mesoderm germ layer. Unlike other mammalian species (eg. mouse) the endometrium of the human uterus develops prenatally during gestation. Little is known about the developmental process involved. A better understanding of human endometrial development may shed light on the mechanisms involved in endometrial regeneration and pathogenesis of adult proliferative endometrial diseases. Mouse neonatal uterine mesenchyme (mNUM) is inductive and can maintain the phenotype of normal adult human endometrial epithelial cells [1]. Both adult human endometrial stroma and neonatal mouse endometrial mesenchyme secrete growth factors of the TGF-beta family including BMPs which have been shown to play an important role in differentiation of human embryonic stem cells (HESC) [2, 3]. Hypothesis: mNUM will direct differentiation of HESC to form Mullerian Duct-like epithelium. Aim: to investigate the role of mNUM in differentiating HESC in vitro and in vivo using A tissue recombination technique. Method: Embryoid bodies (EB) were formed from GFP labelled HESC (ENVY) and GFP-MIXL1 HESC reporter line [4, 5] and recombined with 2 × 0.5 mm pieces of day 1 epithelial cell-free mNUM. Recombinant tissues were either harvested for gene expression analysis or grafted under the kidney capsule of NOD/SCID mice. Results: We found by qRT-PCR that mNUM induces HESC to form mesendoderm/mesoderm progenitors in vitro, obligate intermediates of the developing Mullerian Duct. After further incubation in vivo under the guidance of mNUM, HESC differentiated to form duct-like structures comprising mesoepithelial cells that co-expressed several key developmental proteins of the Mullerian Duct including Emx2, Pax2, Hoxa10, CA125, and also intermediate filament markers such as CK8/18, Vimentin (n = 8). Conclusion: Our study demonstrated for the first time that mNUM can direct HESC to form a mesodermally derived epithelium that is Mullerian Duct-like, providing a novel model for studying human uterine development. (1) Kurita T, et al., The activation function-1 domain of estrogen receptor alpha in uterine stromal cells is required for mouse but not human uterine epithelial response to estrogen. Differentiation, 2005. 73(6): 313–22.(2) Hu J, Gray CA, Spencer TE, Gene expression profiling of neonatal mouse uterine development. Biol Reprod, 2004. 70(6): 1870–6.(3) Stoikos CJ, et al., A distinct cohort of the TGFbeta superfamily members expressed in human endometrium regulate decidualization. Hum Reprod, 2008. 23(6): 1447–56.(4) Davis R, et al., Targeting a GFP reporter gene to the MIXL1 locus of human embryonic stem cells identifies human primitive streak-like cells and enables isolation of primitive hematopoietic precursors. Blood, 2008. 111(4): 1876–84.(5) Costa M, et al., The hESC line Envy expresses high levels of GFP in all differentiated progeny. Nat Methods, 2005. 2(4): 259–60.


1975 ◽  
Vol 78 (2) ◽  
pp. 353-363 ◽  
Author(s):  
C. B. Lunan ◽  
B. Greenz

ABSTRACT Specimens of endometrium from the vault, body and lower body regions of the same human uteri were incubated separately for 30 min in vitro in the presence of 1–6 × 10−9m 3H-oestradiol. Uptake into the nuclei was variable but in general the vault region endometrium was least active in nuclear accumulation of the hormone, especially in secretory phase endometrium. This suggests that intra-uterine variations found in oestradiol uptake in vivo are due to regional differences in the state of the tissue itself.


1999 ◽  
Vol 84 (8) ◽  
pp. 2963-2971 ◽  
Author(s):  
P. A. Mote ◽  
R. L. Balleine ◽  
E. M. McGowan ◽  
C. L. Clarke

The human progesterone receptor (PR) is expressed as two isoforms, PRA and PRB, that function as ligand-activated transcription factors. In vitro studies suggest that the isoforms differ functionally and that the relative levels in a target cell may determine the nature and magnitude of response to progesterone. However, it is not known whether the two isoforms are normally coexpressed in vivo. To understand the functional significance of relative PR isoform expression in normal physiology, it is essential to determine whether PRA and PRB are coexpressed in the same cell. This study reports the development of a dual immunofluorescent staining technique to demonstrate PRA and PRB proteins by single cell analysis in the same tissue section of human endometrium during the menstrual cycle. PRA and PRB are coexpressed in target cells of the human uterus. In the glands, PRA and PRB were expressed before subnuclear vacuole formation and glycogenolysis, implicating both isoforms in this process, whereas persistence of PRB during the midsecretory phase suggested its significance in glandular secretion. In the stroma, the predominance of PRA throughout the cycle implicates this isoform in postovulatory progesterone-mediated events. These results support the view that PRA and PRB mediate distinct pathways of progesterone action in the glandular epithelium and stroma of the human uterus throughout the menstrual cycle.


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