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Induction of Maternal Immune Activation in Mice at Mid-gestation Stage with Viral Mimic Poly(I:C)
Published on: March 25, 2016
Maternally derived immunoglobulin light chain is present in the fetal mammalian CNS
1Neurosciences Graduate Program, Department of Pharmacology, School of Medicine, University of California, San Diego, La Jolla, California 92093-0636, USA.
Insights
Maternally derived immunoglobulin light chain is present in the fetal mouse central nervous system (CNS). This finding suggests a novel maternal contribution to neural development, potentially influencing cerebral cortical development.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Cell-cell interactions are crucial for cerebral cortical development.
- Immunoglobulin-like immunoreactivity (Ig-ir) has been observed in the developing murine cortex.
Purpose of the Study:
- To identify molecules involved in cell-cell interactions during cerebral cortical development.
- To investigate the nature and source of Ig-ir in the fetal murine CNS.
Main Methods:
- Immunohistochemistry on embryonic day 16 murine cortex, hindbrain, and spinal cord.
- Western blot analysis of wild-type and RAG-1/RAG-2 knockout mouse brains.
- Analysis of Ig-ir in RAG-1 +/- embryos from RAG-1-/- mothers and serum injection experiments.
Main Results:
- Intense Ig-ir was detected in specific regions of the embryonic CNS, absent in RAG-1/RAG-2 deficient mice.
- A 25 kDa protein, identified as Ig kappa light chain, was present in wild-type but not knockout brains.
- Maternal serum injection partially reproduced Ig-ir in knockout embryos, indicating a maternal source.
Conclusions:
- Maternally derived immunoglobulin light chain is present in the fetal murine CNS.
- This represents a potential novel maternal contribution to fetal neural development.
- Immunoglobulin molecules may mediate cortical developmental events.
Abstract:
Toward identifying molecules involved in cell-cell interactions during cerebral cortical development, we have investigated the nature of immunoglobulin-like immunoreactivity (Ig-ir) in the murine cortex. Immunohistochemistry using several antisera recognizing IgG revealed intense immunoreactivity in the subplate and marginal zone of embryonic day 16 cortex, as well as in the hindbrain and spinal cord, particularly within ventral fiber tracts. In three independently derived mouse strains lacking the recombination activating genes RAG-1 or RAG-2, which are essential for Ig production, Ig-ir was absent from the fetal CNS. Western blot analyses of wild-type brains from embryonic day 12 through birth identified a 25 kDa protein that co-migrated with Ig light chain and was absent from RAG-1 or RAG-2 -/- brain samples. This result could be replicated with an antiserum specific for Ig kappa light chain, but not with antisera specific for Ig gamma or mu heavy chain. No Ig-ir was detected in the brains of RAG-1 +/- embryos carried by a -/- female, suggesting a maternal source of the immunoreactive molecule. In confirmation of this, Ig-ir could be partially reproduced by intraperitoneal injection of pregnant RAG-1 -/- females with normal mouse serum. We conclude that maternally derived Ig light chain is present in the fetal murine CNS. This may represent a novel maternal contribution to fetal neural development and implicates Ig molecules as potential mediators of cortical developmental events.
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