Document Detail


Placental defects in alpha7 integrin null mice.
MedLine Citation:
PMID:  17904217     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The alpha7beta1 integrin is a heterodimeric transmembrane receptor that links laminin in the extracellular matrix to the cell cytoskeleton. Loss of the alpha7 integrin chain results in partial embryonic lethality. We have previously shown that alpha7 integrin null embryos exhibit vascular smooth muscle cell defects that result in cerebral vascular hemorrhaging. Since the placenta is highly vascularized, we hypothesized that placental vascular defects in alpha7 integrin null embryos may contribute to the partial embryonic lethality. Placentae from embryonic day (ED) 9.5 and 13.5 alpha7 integrin knockout embryos showed structural defects including infiltration of the spongiotrophoblast layer into the placental labyrinth, a reduction in the placental labyrinth and loss of distinct placental layers. Embryos and placentae that lacked the alpha7 integrin weighed less compared to wild-type controls. Blood vessels within the placental labyrinth of alpha7 integrin null embryos exhibited fewer differentiated vascular smooth muscle cells compared to wild-type. Loss of the alpha7 integrin resulted in altered extracellular matrix deposition and reduced expression of alpha5 integrin. Together our results confirm a role for the alpha7beta1 integrin in placental vascular development and demonstrate for the first time that loss of the alpha7 integrin results in placental defects.
Authors:
J V Welser; N D Lange; N Flintoff-Dye; H R Burkin; D J Burkin
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2007-09-27
Journal Detail:
Title:  Placenta     Volume:  28     ISSN:  0143-4004     ISO Abbreviation:  Placenta     Publication Date:    2007 Nov-Dec
Date Detail:
Created Date:  2007-10-22     Completed Date:  2008-09-08     Revised Date:  2011-06-02    
Medline Journal Info:
Nlm Unique ID:  8006349     Medline TA:  Placenta     Country:  England    
Other Details:
Languages:  eng     Pagination:  1219-28     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, University of Nevada, Reno, NV 89557, USA.
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MeSH Terms
Descriptor/Qualifier:
Animals
Antigens, CD / genetics*,  metabolism
Blotting, Western
Endothelium, Vascular / metabolism,  pathology
Extracellular Matrix / metabolism,  pathology
Female
Fetal Death / genetics
Fetal Weight / genetics
Immunohistochemistry
Integrin alpha Chains / deficiency*,  genetics*,  metabolism
Mice
Mice, Inbred C57BL
Mice, Knockout
Muscle, Smooth, Vascular / pathology
Placenta / blood supply*,  growth & development,  pathology
Placenta Diseases / genetics*,  pathology
Pregnancy
Grant Support
ID/Acronym/Agency:
P20 RR015581-059004/RR/NCRR NIH HHS; P20 RR015581-069004/RR/NCRR NIH HHS; P20 RR015581-076560/RR/NCRR NIH HHS; P20 RR018751-01/RR/NCRR NIH HHS; P20 RR018751-010001/RR/NCRR NIH HHS; P20 RR018751-020001/RR/NCRR NIH HHS; P20 RR018751-030001/RR/NCRR NIH HHS; P20 RR018751-035832/RR/NCRR NIH HHS; P20 RR018751-047407/RR/NCRR NIH HHS; P20 RR15581-04/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
0/Antigens, CD; 0/Integrin alpha Chains; 0/integrin alpha7
Comments/Corrections

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