scholarly journals Bovine trophoblastic cell differentiation and binucleation involves enhanced endogenous retrovirus element expression

2012 ◽  
Vol 10 (1) ◽  
pp. 41 ◽  
Author(s):  
Katsuo Koshi ◽  
Yasunori Suzuki ◽  
Yuki Nakaya ◽  
Kei Imai ◽  
Misa Hosoe ◽  
...  
2012 ◽  
Vol 87 (Suppl_1) ◽  
pp. 379-379
Author(s):  
Katsuo Koshi ◽  
Yasunori Suzuki ◽  
Yuki Nakaya ◽  
Kei Imai ◽  
Misa Hosoe ◽  
...  

2001 ◽  
Vol 307 (2) ◽  
pp. 225-235 ◽  
Author(s):  
Haruo Nakano ◽  
Arata Shimada ◽  
Kei Imai ◽  
Toshiaki Takezawa ◽  
Toru Takahashi ◽  
...  

1997 ◽  
Vol 45 (4) ◽  
pp. 569-581 ◽  
Author(s):  
Matti Korhonen ◽  
Ismo Virtanen

We studied the distribution of laminin (Ln) α1–α3, β1–β3, and γ1 chains, and of the extradomain-A (EDA) and EDB and the oncofetal epitope of fibronectin (Onc-Fn) in extravillous trophoblastic cells and decidua in the human placenta by immunohistochemistry. We found that the transition from villous to extravillous trophoblast was accompanied by emergence of immunoreactivity for EDA-, EDB-, and Onc-Fn among the cells. Furthermore, whereas the villous trophoblastic basement membrane (BM) contains Ln α1, α2, β1, β2, and γ1 chains, immunoreactivity for Ln α1, β1, and γ1, but not for Ln α2 and β2 chains, was detected in association with extravillous trophoblastic cells. Interestingly, although immunoreactivity for the Ln α1, α2, β1, β2, and γ1 chains was detected in all decidual cell BMs, EDB-Fn and Onc-Fn were detected only in decidua that had been invaded by the trophoblast. In summary, our results describe distinct changes in the distribution of Ln and Fn isoforms during the differentiation of villous trophoblast into extravillous trophoblastic cells. Furthermore, EDB- and Onc-Fn are preferentially found in decidua that has been invaded by the trophoblast, indicating that the deposition of these Fn isoforms reflects a decidual cell response to invasion.


2013 ◽  
Vol 74 (5) ◽  
pp. 721-732 ◽  
Author(s):  
David Kremer ◽  
Tanja Schichel ◽  
Moritz Förster ◽  
Nevena Tzekova ◽  
Corinne Bernard ◽  
...  

2002 ◽  
Vol 307 (2) ◽  
pp. 273-273
Author(s):  
Haruo Nakano ◽  
Arata Shimada ◽  
Kei Imai ◽  
Toshiaki Takezawa ◽  
Toru Takahashi ◽  
...  

2019 ◽  
Vol 20 (14) ◽  
pp. 3457 ◽  
Author(s):  
Árpád Ferenc Kovács ◽  
Nóra Fekete ◽  
Lilla Turiák ◽  
András Ács ◽  
László Kőhidai ◽  
...  

Regulatory T cells (Treg) are mandatory elements in the maintenance of human pregnancy, but their de novo differentiation has not been completely exposed. HSPE1 chaperone expressing trophoblast cells may have a role in it. Trophoblast-derived extracellular vesicles (EVs), either at the feto–maternal interface or in circulation, target CD4+ T cells. We hypothesized that HSPE1-associated trophoblastic cell line (BeWo)-derived EVs are active mediators of Treg cell differentiation. We proved at first that recombinant HSPE1 promote human Treg cell differentiation in vitro. Developing a CRISPR-Cas9 based HSPE1 knockout BeWo cell line we could also demonstrate, that EV-associated HSPE1 induces Treg development. Next-generation sequencing of miRNA cargo of BeWo-EVs characterized the regulatory processes of Treg polarization. By the use of single-cell transcriptomics analysis, seven Treg cell subtypes were distinguished and we demonstrated for the first time that the expression level of HSPE1 was Treg subtype dependent, and CAPG expression is characteristic to memory phenotype of T cells. Our data indicate that HSPE1 and CAPG may be used as markers for identification of Treg subtypes. Our results suggest, that trophoblastic-derived iEVs-associated HSPE1 and miRNA cargo have an important role in Treg cell expansion in vitro and HSPE1 is a useful marker of Treg subtype characterization.


2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Yangquan Xiang ◽  
Hongqing Liang

Endogenous retroviruses (ERVs) are repetitive sequences in the genome, belonging to the retrotransposon family. During the course of life, ERVs are associated with multiple aspects of chromatin and transcriptional regulation in development and pathological conditions. In mammalian embryos, ERVs are extensively activated in early embryo development, but with a highly restricted spatial-temporal pattern; and they are drastically silenced during differentiation with exceptions in extraembryonic tissue and germlines. The dynamic activation pattern of ERVs raises questions about how ERVs are regulated in the life cycle and whether they are functionally important to cell fate decision during early embryo and somatic cell development. Therefore, in this review, we focus on the pieces of evidence demonstrating regulations and functions of ERVs during stem cell differentiation, which suggests that ERV activation is not a passive result of cell fate transition but the active epigenetic and transcriptional regulation during mammalian development and stem cell differentiation.


Author(s):  
Mitsuko Masutani ◽  
Tadashige Nozaki ◽  
Masatoshi Watanabe ◽  
Takahiro Ochiya ◽  
Fumio Hasegawa ◽  
...  

1992 ◽  
Vol 12 (11) ◽  
pp. 4824-4833
Author(s):  
B T Lamb ◽  
K Satyamoorthy ◽  
D Solter ◽  
A Basu ◽  
M Q Xu ◽  
...  

The retinoic acid-induced differentiation of F9 cells into parietal endoderm-like cells activates transcription of the endogenous mouse retrovirus, the intracisternal A-particle (IAP). To investigate the elements that control IAP gene differentiation-specific expression, we used methylation interference, Southwestern (DNA-protein), and transient-transfection assays and identified the IAP-proximal enhancer (IPE) element that directs differentiation-specific expression. We find that the IPE is inactive in undifferentiated F9 cells and active in differentiated parietal endoderm-like PYS-2 cells. Three proteins of 40, 60, and 68 kDa bind to the sequence GAGTAGAC located between nucleotides -53 and -47 within the IPE. The 40- and 68-kDa proteins from both the undifferentiated and differentiated cells exhibit similar DNA-binding activities. However, the 60-kDa protein from differentiated cells has greater binding activity than that from undifferentiated cells, suggesting a role for this protein in F9 differentiation-specific expression of the IAP gene. The IAP gene is negatively regulated by the adenovirus E1A proteins, and the E1A sequence responsible for repression is located at the N terminus, between amino acids 2 and 67. The DNA sequence that is the target of E1A repression also maps to the IPE element. Colocalization of the differentiation-specific and E1A-sensitive elements to the same protein-binding site within the IPE suggests that the E1A-like activity functions in F9 cells to repress IAP gene expression. Activation of the IAP gene may result when the E1A-like activity is lost or inactivated during F9 cell differentiation, followed by binding of the 60-kDa positive regulatory protein to the enhancer element.


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