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The Journal of Immunology
Article . 2013 . Peer-reviewed
License: OUP Standard Publication Reuse
Data sources: Crossref
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C5a Receptor Signaling Prevents Folate Deficiency–Induced Neural Tube Defects in Mice

Authors: Denny, Kerina J.; Coulthard, Liam G.; Jeanes, Angela; Lisgo, Steven; Simmons, David G.; Callaway, Leonie K.; Wlodarczyk, Bogdan; +3 Authors

C5a Receptor Signaling Prevents Folate Deficiency–Induced Neural Tube Defects in Mice

Abstract

Abstract The complement system is involved in a range of diverse developmental processes, including cell survival, growth, differentiation, and regeneration. However, little is known about the role of complement in embryogenesis. In this study, we demonstrate a novel role for the canonical complement 5a receptor (C5aR) in the development of the mammalian neural tube under conditions of maternal dietary folic acid deficiency. Specifically, we found C5aR and C5 to be expressed throughout the period of neurulation in wild-type mice and localized the expression to the cephalic regions of the developing neural tube. C5aR was also found to be expressed in the neuroepithelium of early human embryos. Ablation of the C5ar1 gene or the administration of a specific C5aR peptide antagonist to folic acid–deficient pregnant mice resulted in a high prevalence of severe anterior neural tube defect-associated congenital malformations. These findings provide a new and compelling insight into the role of the complement system during mammalian embryonic development.

Keywords

Male, Neural Tube, Complement system, 571, Folic Acid Deficiency, Mice, Pregnancy, Morphogenesis, Animals, Humans, Neural Tube Defects, RNA, Messenger, Neurulation, Receptor, Anaphylatoxin C5a, Mice, Knockout, 2403 Immunology, Complement C5, Embryo, Mammalian, Disease Models, Animal, Protein Transport, Embryogenesis, Female, Signal Transduction

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    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
44
Top 10%
Top 10%
Top 10%
bronze