scholarly journals Corrigendum: Vascular development and hemodynamic force in the mouse yolk sac

2014 ◽  
Vol 5 ◽  
Author(s):  
Monica D. Garcia ◽  
Irina V. Larina
Development ◽  
2000 ◽  
Vol 127 (19) ◽  
pp. 4179-4193 ◽  
Author(s):  
O. Kruger ◽  
A. Plum ◽  
J.S. Kim ◽  
E. Winterhager ◽  
S. Maxeiner ◽  
...  

In order to reveal the biological function(s) of the gap-junction protein connexin 45 (Cx45), we generated Cx45-deficient mice with targeted replacement of the Cx45-coding region with the lacZ reporter gene. Heterozygous Cx45(+/)(−) mice showed strong expression of the reporter gene in vascular and visceral smooth muscle cells. Cx45-deficient embryos exhibited striking abnormalities in vascular development and died between embryonic day (E) 9.5 and 10.5. Differentiation and positioning of endothelial cells appeared to be normal, but subsequent development of blood vessels revealed impaired formation of vascular trees in the yolk sac, impaired allantoic mesenchymal ingrowth and capillary formation in the labyrinthine part of the placenta, and arrest of arterial growth, including a failure to develop a smooth muscle layer surrounding the major arteries of the embryo proper. As a consequence, the hearts of most Cx45-deficient embryos were dilated. The abnormal development of the vasculature in the yolk sac of Cx45(−)(/)(−) embryos could be caused by defective TGFbeta signalling, as the amount of TGF beta1 protein in the epithelial layer of the yolk sac was largely decreased in the E9.5 Cx45(−)(/)(−) embryo, compared with the wild-type embryo. The defective vascular development was accompanied by massive apoptosis, which began in some embryos at E8.5 and was abundant in virtually all tissues of the embryos at E9.5. We conclude that in Cx45(−)(/)(−) embryos, vasculogenesis was normal, but subsequent transformation into mature vessels was interrupted. Development of different types of vessels was impaired to a varying extent, which possibly reflects the complementation by other connexin(s).


2013 ◽  
Vol 110 (10) ◽  
pp. 3800-3805 ◽  
Author(s):  
T. Tasaki ◽  
S. T. Kim ◽  
A. Zakrzewska ◽  
B. E. Lee ◽  
M. J. Kang ◽  
...  

2009 ◽  
Vol 387 (4) ◽  
pp. 754-759 ◽  
Author(s):  
Hoshimi Kanemura ◽  
Takaya Satoh ◽  
Shymaa E. Bilasy ◽  
Shuji Ueda ◽  
Masanori Hirashima ◽  
...  

Placenta ◽  
2014 ◽  
Vol 35 (9) ◽  
pp. A48-A49
Author(s):  
Andrea Mess ◽  
Ana Claudia Carreira ◽  
Paula Fratini ◽  
Phelipe Favaron ◽  
Flavio Meirelles ◽  
...  

2007 ◽  
Vol 28 (1) ◽  
pp. 282-292 ◽  
Author(s):  
Jason Beliakoff ◽  
Jane Lee ◽  
Hiroo Ueno ◽  
Aparna Aiyer ◽  
Irving L. Weissman ◽  
...  

ABSTRACT Members of the PIAS (for protein inhibitor of activated STAT) family play critical roles in modulating the activity of a variety of transcriptional regulators. Zimp10, a novel PIAS-like protein, is a transcriptional coregulator and may be involved in the modification of chromatin through interactions with the SWI/SNF chromatin-remodeling complexes. Here, we investigate the biological role of Zimp10 in zimp10-deficient mice. Homozygosity for the Zimp10-targeted allele resulted in developmental arrest at approximately embryonic day 10.5. Analysis of knockout embryos revealed severe defects in the reorganization of the yolk sac vascular plexus. No significant abnormality in hematopoietic potential was observed in zimp10 null mice. Microarray and quantified reverse transcription-PCR analyses showed that the expression of the Fos family member Fra-1, which is involved in extraembryonic vascular development, was reduced in yolk sac tissues of zimp10 null embryos. Using fra-1 promoter/reporter constructs, we further demonstrate the regulatory role of Zimp10 on the transcription of Fra-1. This study provides evidence to demonstrate a crucial role for Zimp10 in vasculogenesis.


Development ◽  
2007 ◽  
Vol 134 (18) ◽  
pp. 3317-3326 ◽  
Author(s):  
J. L. Lucitti ◽  
E. A. V. Jones ◽  
C. Huang ◽  
J. Chen ◽  
S. E. Fraser ◽  
...  

Author(s):  
William P. Jollie

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.


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