Immunolocalization of bcl-2 protein in human endometrium in the menstrual cycle and simulated early pregnancy

1995 ◽  
Vol 1 (4) ◽  
pp. 157-162 ◽  
Author(s):  
E.A.T. Koh ◽  
P.J. IIIingworth ◽  
W.C. Duncan ◽  
H.O.D. Critchley
2005 ◽  
Vol 17 (9) ◽  
pp. 95
Author(s):  
C. Freyer ◽  
L. Kilpatrick ◽  
L. Salamonsen ◽  
G. Nie

Furin is a proprotein convertase (PC) implicated in the endoproteolytic maturation of inactive protein precursors of growth factors, hormones, receptors, and viral envelope glycoproteins.1 Two functionally active forms of furin, one membrane-bound containing a C-terminal transmembrane domain (TD) and a cytoplasmic tail (CT), and one soluble without the TD and CT, have been characterised. We have previously shown that PC6, one of the PCs closely related to furin, is expressed in the human endometrium and is closely associated with decidualization of stromal cells during implantation.2 Although furin is ubiquitously expressed, its expression in the human endometrium is unknown. In this study, we investigated the spatial and temporal expression pattern of furin in the human endometrium using RT-PCR and immunohistochemistry. While furin expression is detected throughout the menstrual cycle and during early pregnancy, lowest mRNA levels are seen during the proliferative phase. Using an antibody directed against the C-terminus of the membrane bound form, furin is detected in the stroma, glandular and luminal epithelium, as well as in endothelia and neutrophils throughout the menstrual cycle and during early pregnancy. In the stroma, highest levels of furin are present during menstruation (n = 3), they are also high during the proliferative phase (n = 4), but significantly lower levels are detected during the secretory phase (n = 10, P < 0.05, Tukey HSD). In the first trimester decidua, furin is present in well decidualised stromal cells. The overall expression pattern of furin is different to that of PC6; in particular, furin expression is associated only with well decidualized stromal cells whereas PC6 is involved in the initial stages of decidualization. These data suggest that furin and PC6 play different roles in the human endometrium, especially during embryo implantation. (1)Nakayama K. (1997). Biochem. J. 327, 625–635.(2)Nie et al. (2005). Biol. Reprod. 72, 1029–1036.


1971 ◽  
Vol 111 (8) ◽  
pp. 1064-1068 ◽  
Author(s):  
Kobchitt Limpaphayom ◽  
Chung Lee ◽  
Herbert I. Jacobson ◽  
Theodore M. King

2002 ◽  
Vol 78 ◽  
pp. S168
Author(s):  
Umit A Kayisli ◽  
Ozlem Guzelolgu-Kayisli ◽  
Murat Berkkanoglu ◽  
Aydin Arici

1998 ◽  
Vol 69 (1) ◽  
pp. 37-40 ◽  
Author(s):  
Eleonora Lanteri ◽  
Maurizio Pistritto ◽  
Giovanni Bartoloni ◽  
Sebastiano Cordaro ◽  
Franca Stivala ◽  
...  

1996 ◽  
Vol 11 (5) ◽  
pp. 1073-1078 ◽  
Author(s):  
N. Sugino ◽  
K. Shimamura ◽  
S. Takiguchi ◽  
H. Tamura ◽  
M. Ono ◽  
...  

Reproduction ◽  
2011 ◽  
Vol 142 (2) ◽  
pp. 345-352 ◽  
Author(s):  
Linsay J Macdonald ◽  
Sheila C Boddy ◽  
Fiona C Denison ◽  
Kurt J Sales ◽  
Henry N Jabbour

Lipoxin A4is a lipid mediator that elicits anti-inflammatory and pro-resolution actions via its receptor, formyl peptide receptor 2 (FPR2/ALX). In this study, we aimed to investigate the expression and potential role of lipoxin A4and FPR2/ALX in the regulation of inflammation associated with cyclical remodeling of the human endometrium across the menstrual cycle and during early pregnancy. Using quantitative RT-PCR analysis, we found that FPR2/ALX expression is upregulated during the menstrual phase of the cycle and in decidua tissue from the first trimester of pregnancy. We localized the site of expression of FPR2/ALX in menstrual phase endometrium and first-trimester decidua tissue to glandular epithelial cells and cells within the stromal compartment, including cells lining the blood vessels and immune cells. Measurement of serum lipoxin A4by ELISA revealed no difference in its levels across the menstrual cycle but an elevation in early pregnancy (P<0.001). We found that lipoxin A4was regulated by human chorionic gonadotrophin (hCG) during early pregnancy, because treatment of human decidua tissue with hCG increased lipoxin A4release (P<0.01). Finally, we have shown that lipoxin A4can suppress phorbol myristate acetate-induced expression of the inflammatory cytokines interleukin 6 and 8 in human endometrium and decidua tissue. These results demonstrate for the first time that lipoxin A4and its receptor FPR2/ALX can regulate inflammatory events in the human endometrium and decidua of early pregnancy.


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