Ultrastructural localization of aminopeptidase A/angiotensinase and placental leucine aminopeptidase/oxytocinase in chorionic villi of human placenta

2003 ◽  
Vol 71 (1) ◽  
pp. 29-37 ◽  
Author(s):  
Norio Ito ◽  
Seiji Nomura ◽  
Akira Iwase ◽  
Tomomi Ito ◽  
Kazuhiko Ino ◽  
...  
1984 ◽  
Vol 119 (1) ◽  
pp. 18-26 ◽  
Author(s):  
Ramazan Demir ◽  
Türkân Erbengi

1996 ◽  
Vol 149 (2) ◽  
pp. 249-258 ◽  
Author(s):  
S McCracken ◽  
J E Layton ◽  
S C Shorter ◽  
P M Starkey ◽  
D H Barlow ◽  
...  

Abstract The development of the placenta is dependent upon the regulated proliferation, invasion and differentiation of trophoblast. Expression of cytokines at the feto-maternal interface suggests that these molecules may participate in placentation. The expression of granulocyte-colony stimulating factor (G-CSF) and G-CSF receptor (G-CSFR) during the development of the human placenta was studied by immunohistochemistry using an anti-G-CSF monoclonal antibody (mAb) and two novel anti-G-CSFR mAbs. G-CSF was present in the stroma of fetal chorionic villi and maternal decidual tissues throughout pregnancy. G-CSFR was detected at high levels in fetal first and third, but not second trimester placental tissues. Staining for G-CSFR was undetectable in maternal decidual tissue from all gestational stages. In first trimester tissues, staining for placental G-CSFR was strongest in differentiated syncytiotrophoblast and invasive, extravillous cytotrophoblast, and weak staining was evident in undifferentiated cytotrophoblast. Immunohistochemical data suggesting temporal regulation of G-CSFR were corroborated by Western blotting and amplification by reverse transcription and PCR of G-CSFR mRNA. These data suggested that expression of G-CSFR in the human placenta is regulated both temporally and spatially, and that placental G-CSF is involved in paracrine regulation, and indicate a role for G-CSF and G-CSFR in trophoblast growth or function during placentation. Journal of Endocrinology (1996) 149, 249–258


Planta ◽  
2011 ◽  
Vol 234 (4) ◽  
pp. 857-863 ◽  
Author(s):  
Latifa Boulila-Zoghlami ◽  
Philippe Gallusci ◽  
Frances M. Holzer ◽  
Gilles J. Basset ◽  
Whabi Djebali ◽  
...  

1993 ◽  
Vol 30 (2-3) ◽  
pp. 136-145 ◽  
Author(s):  
CAROLYN J.P. JONES ◽  
MICHAELE HARTMANN ◽  
ASTRID BLASCHITZ ◽  
GERNOT DESOYE

Placenta ◽  
2000 ◽  
Vol 21 (7) ◽  
pp. 628-634 ◽  
Author(s):  
Y. Nakanishi ◽  
S. Nomura ◽  
M. Okada ◽  
T. Ito ◽  
Y. Katsumata ◽  
...  

1985 ◽  
Vol 227 (1) ◽  
pp. 317-326 ◽  
Author(s):  
R S Tuan

The Ca2+-binding protein (HCaBP) of the human placenta was studied with respect to its biochemical properties, tissue and cellular distribution, and possible involvement in placental Ca2+ transport. Optimal Ca2+ binding by the HCaBP occurs at pH 7-8 and in 100 mM-Na+ and 3 mM-Ca2+. The HCaBP possesses at least 10 Ca2+-binding sites with a Kd of 5 × 10(-6) M ([Ca2+]). Highly specific rabbit-derived anti-HCaBP antibodies were used for HCaBP immunoquantification and immunohistochemistry, which revealed that the HCaBP is localized in the chorionic villi and is primarily associated with the trophoblastic cells of the placenta. In addition, an ‘in vitro’ cell-free assay system for Ca2+ uptake was constructed with microsomal membranes isolated from term placental tissues. Ca2+ uptake by the placental microsomal fraction exhibited characteristics indicative of active Ca2+ transport such as temperature-dependence, saturability and energetic requirement. In this system, preincubation of microsomal membranes with anti-HCaBP antibodies inhibited Ca2+ uptake, suggesting that the HCaBP is functionally involved in placental membrane Ca2+ uptake.


Ensho Saisei ◽  
2005 ◽  
Vol 25 (2) ◽  
pp. 102-106
Author(s):  
Xiaohong Zhang ◽  
Kouichi Igura ◽  
Kenji Takahashi ◽  
Ayako Mitsuru ◽  
Tsuneo A. Takahashi

2019 ◽  
Vol 11 (6) ◽  
pp. 447-456 ◽  
Author(s):  
Michael Z. Zulu ◽  
Fernando O. Martinez ◽  
Siamon Gordon ◽  
Clive M. Gray

In this review, we discuss the often overlooked tissue-resident fetal macrophages, Hofbauer cells, which are found within the chorionic villi of the human placenta. Hofbauer cells have been shown to have a phenotype associated with regulatory and anti-inflammatory functions. They are thought to play a crucial role in the regulation of pregnancy and in the maintenance of a homeostatic environment that is crucial for fetal development. Even though the numbers of these macrophages are some of the most abundant immune cells in the human placenta, which are sustained throughout pregnancy, there are very few studies that have identified their origin, their phenotype, and functions and why they are maintained throughout gestation. It is not yet understood how Hofbauer cells may change in function throughout normal pregnancy, and especially in those complicated by maternal gestational diabetes, preeclampsia, and viral infections, such as Zika, cytomegalovirus, and human immunodeficiency virus. We review what is known about the origin of these macrophages and explore how common complications of pregnancy dysregulate these cells leading to adverse birth outcomes in humans. Our synthesis sheds light on areas for human studies that can further define these innate regulatory cells.


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