Unilateral Effects of Pregnancy on Differential Expression of the Gap Junction Proteins Connexin 43 and 37 in Ovine Uterine Artery Endothelium.

2010 ◽  
Vol 83 (Suppl_1) ◽  
pp. 477-477
Author(s):  
Timothy J. Morschauser ◽  
Jayanth Ramadoss ◽  
Jill M. Koch ◽  
Gladys E. Lopez ◽  
Ian M. Bird ◽  
...  
2013 ◽  
Vol 2013 ◽  
pp. 1-11 ◽  
Author(s):  
Anna Hejmej ◽  
Malgorzata Kotula-Balak ◽  
Katarzyna Chojnacka ◽  
Paulina Kuras ◽  
Marta Lydka-Zarzycka ◽  
...  

In the present study we evaluatedin vivoandin vitroeffects of 4-tert-octylphenol (OP) on the expression and distribution of adherens and gap junction proteins, N-cadherin,β-catenin, and connexin 43 (Cx43), in testes of seasonally breeding rodents, bank voles. We found that in bank vole testes expression and distribution of N-cadherin,β-catenin, and Cx43 were photoperiod dependent. Long-term treatment with OP (200 mg/kg b.w.) resulted in the reduction of junction proteins expressions (P<0.05,P<0.01) and their delocalization in the testes of males kept in long photoperiod, whereas in short-day animals slight increase of Cx43 (P<0.05), N-cadherin, andβ-catenin (statistically nonsignificant) levels was observed. Effects of OP appeared to be independent of FSH and were maintained duringin vitroorgan culture, indicating that OP acts directly on adherens and gap junction proteins in the testes. An experiment performed using an antiestrogen ICI 182,780 demonstrated that the biological effects of OP onβ-catenin and Cx43 involve an estrogen receptor-mediated response. Taken together, in bank vole organization of adherens and gap junctions and their susceptibility to OP are related to the length of photoperiod. Alterations in cadherin/catenin and Cx43-based junction may partially result from activation of estrogen receptorαand/orβsignaling pathway.


2004 ◽  
Vol 1 (1) ◽  
pp. 44-54 ◽  
Author(s):  
A. Salameh ◽  
K. Muhlberg . ◽  
P. Schneider . ◽  
S. Dhein . ◽  
D. Pfeiffer .

2007 ◽  
Vol 85 (5) ◽  
pp. 945-953 ◽  
Author(s):  
W.A. Roscoe ◽  
E. Messersmith ◽  
A. Meyer-Franke ◽  
B. Wipke ◽  
S.J. Karlik

2006 ◽  
Vol 126 (2) ◽  
pp. 138-143 ◽  
Author(s):  
Yun-Hoon Choung ◽  
Keehyun Park ◽  
Sung-Ook Kang ◽  
Alexander Markov Raynov ◽  
Chul Ho Kim ◽  
...  

1990 ◽  
Vol 110 (3) ◽  
pp. 597-605 ◽  
Author(s):  
R L Gimlich ◽  
N M Kumar ◽  
N B Gilula

Xenopus mRNAs that potentially encode gap junction proteins in the oocyte and early embryo have been identified by low-stringency screening of cDNA libraries with cloned mammalian gap junction cDNAs. The levels of these mRNAs show strikingly different temporal regulation and tissue distribution. Using a nomenclature designed to stress important structural similarities of distinct gap junction gene products, the deduced polypeptides have been designated the Xenopus alpha 1 and alpha 2 gap junction proteins. The alpha 2 gap junction mRNA is a maternal transcript that disappears by the late gastrula stage. It is not detected in any organ of the adult except the ovary, and resides primarily, if not exclusively, in the oocytes and early embryos. The alpha 1 gap junction mRNA appears during organogenesis, and is detected in RNA from a wide variety of organs. It is also found in full-grown oocytes, but is rapidly degraded upon oocyte maturation, both in vivo and in vitro. The alpha 1 and alpha 2 mRNAs encode proteins with different degrees of amino acid sequence similarity to the predominant gap junction subunit of the mammalian heart (connexin 43). Together with our earlier report of a mid-embryonic (beta 1) gap junction mRNA, the results suggest that intercellular communication during oocyte growth and postfertilization development is a complex phenomenon involving the coordinated regulation of several genes.


2001 ◽  
Vol 115 (4) ◽  
pp. 277-284 ◽  
Author(s):  
Ichiro Yamanaka ◽  
Akio Kuraoka ◽  
Tetsuichiro Inai ◽  
Tatsuro Ishibashi ◽  
Yosaburo Shibata

1989 ◽  
Vol 86 (24) ◽  
pp. 10148-10152 ◽  
Author(s):  
R. Dermietzel ◽  
O. Traub ◽  
T. K. Hwang ◽  
E. Beyer ◽  
M. V. Bennett ◽  
...  

1998 ◽  
Vol 82 (5) ◽  
pp. 604-612 ◽  
Author(s):  
King F. Kwong ◽  
Richard B. Schuessler ◽  
Karen G. Green ◽  
James G. Laing ◽  
Eric C. Beyer ◽  
...  

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