Differential neuronal and glial expression of nuclear factor I proteins in the cerebral cortex of adult mice
The nuclear factor I (NFI) family of transcription factors plays an important role in the development of the cerebral cortex in humans and mice. Disruption of nuclear factor IA (NFIA), nuclear factor IB (NFIB), or nuclear factor IX (NFIX) results in abnormal development of the corpus callosum, later...
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Published in | Journal of comparative neurology (1911) Vol. 525; no. 11; pp. 2465 - 2483 |
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Language | English |
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Abstract | The nuclear factor I (NFI) family of transcription factors plays an important role in the development of the cerebral cortex in humans and mice. Disruption of nuclear factor IA (NFIA), nuclear factor IB (NFIB), or nuclear factor IX (NFIX) results in abnormal development of the corpus callosum, lateral ventricles, and hippocampus. However, the expression or function of these genes has not been examined in detail in the adult brain, and the cell type‐specific expression of NFIA, NFIB, and NFIX is currently unknown. Here, we demonstrate that the expression of each NFI protein shows a distinct laminar pattern in the adult mouse neocortex and that their cell type‐specific expression differs depending on the family member. NFIA expression was more frequently observed in astrocytes and oligodendroglia, whereas NFIB expression was predominantly localized to astrocytes and neurons. NFIX expression was most commonly observed in neurons. The NFI proteins were equally distributed within microglia, and the ependymal cells lining the ventricles of the brain expressed all three proteins. In the hippocampus, the NFI proteins were expressed during all stages of neural stem cell differentiation in the dentate gyrus, with higher expression intensity in neuroblast cells as compared to quiescent stem cells and mature granule neurons. These findings suggest that the NFI proteins may play distinct roles in cell lineage specification or maintenance, and establish the basis for further investigation of their function in the adult brain and their emerging role in disease.
This study shows that nuclear factor I (NFI) proteins are expressed in all major cell types in the adult mouse dorsal forebrain, but each member displays a unique cell type‐specific distribution. This comprehensive survey provides a baseline to investigate NFI function in the adult brain. |
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AbstractList | The nuclear factor I (NFI) family of transcription factors plays an important role in the development of the cerebral cortex in humans and mice. Disruption of nuclear factor IA (NFIA), nuclear factor IB (NFIB), or nuclear factor IX (NFIX) results in abnormal development of the corpus callosum, lateral ventricles, and hippocampus. However, the expression or function of these genes has not been examined in detail in the adult brain, and the cell type‐specific expression of NFIA, NFIB, and NFIX is currently unknown. Here, we demonstrate that the expression of each NFI protein shows a distinct laminar pattern in the adult mouse neocortex and that their cell type‐specific expression differs depending on the family member. NFIA expression was more frequently observed in astrocytes and oligodendroglia, whereas NFIB expression was predominantly localized to astrocytes and neurons. NFIX expression was most commonly observed in neurons. The NFI proteins were equally distributed within microglia, and the ependymal cells lining the ventricles of the brain expressed all three proteins. In the hippocampus, the NFI proteins were expressed during all stages of neural stem cell differentiation in the dentate gyrus, with higher expression intensity in neuroblast cells as compared to quiescent stem cells and mature granule neurons. These findings suggest that the NFI proteins may play distinct roles in cell lineage specification or maintenance, and establish the basis for further investigation of their function in the adult brain and their emerging role in disease. The nuclear factor I (NFI) family of transcription factors plays an important role in the development of the cerebral cortex in humans and mice. Disruption of nuclear factor IA (NFIA), nuclear factor IB (NFIB), or nuclear factor IX (NFIX) results in abnormal development of the corpus callosum, lateral ventricles, and hippocampus. However, the expression or function of these genes has not been examined in detail in the adult brain, and the cell type‐specific expression of NFIA, NFIB, and NFIX is currently unknown. Here, we demonstrate that the expression of each NFI protein shows a distinct laminar pattern in the adult mouse neocortex and that their cell type‐specific expression differs depending on the family member. NFIA expression was more frequently observed in astrocytes and oligodendroglia, whereas NFIB expression was predominantly localized to astrocytes and neurons. NFIX expression was most commonly observed in neurons. The NFI proteins were equally distributed within microglia, and the ependymal cells lining the ventricles of the brain expressed all three proteins. In the hippocampus, the NFI proteins were expressed during all stages of neural stem cell differentiation in the dentate gyrus, with higher expression intensity in neuroblast cells as compared to quiescent stem cells and mature granule neurons. These findings suggest that the NFI proteins may play distinct roles in cell lineage specification or maintenance, and establish the basis for further investigation of their function in the adult brain and their emerging role in disease. This study shows that nuclear factor I (NFI) proteins are expressed in all major cell types in the adult mouse dorsal forebrain, but each member displays a unique cell type‐specific distribution. This comprehensive survey provides a baseline to investigate NFI function in the adult brain. |
Author | Piper, Michael Harris, Lachlan Lim, Jonathan W. C. Harvey, Tracey J. Bunt, Jens Richards, Linda J. Gronostajski, Richard M. Chen, Kok‐Siong |
Author_xml | – sequence: 1 givenname: Kok‐Siong surname: Chen fullname: Chen, Kok‐Siong organization: The Queensland Brain Institute, The University of Queensland – sequence: 2 givenname: Lachlan surname: Harris fullname: Harris, Lachlan organization: The University of Queensland – sequence: 3 givenname: Jonathan W. C. surname: Lim fullname: Lim, Jonathan W. C. organization: The Queensland Brain Institute, The University of Queensland – sequence: 4 givenname: Tracey J. surname: Harvey fullname: Harvey, Tracey J. organization: The University of Queensland – sequence: 5 givenname: Michael surname: Piper fullname: Piper, Michael organization: The University of Queensland – sequence: 6 givenname: Richard M. surname: Gronostajski fullname: Gronostajski, Richard M. organization: Program in Genetics, Genomics and Bioinformatics, Center of Excellence in Bioinformatics and Life Sciences, State University of New York at Buffalo – sequence: 7 givenname: Linda J. surname: Richards fullname: Richards, Linda J. email: richards@uq.edu.au organization: The University of Queensland – sequence: 8 givenname: Jens orcidid: 0000-0003-0397-2019 surname: Bunt fullname: Bunt, Jens email: j.bunt@uq.edu.au organization: The Queensland Brain Institute, The University of Queensland |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28295292$$D View this record in MEDLINE/PubMed |
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Keywords | cortex RRID: AB_10712361 NFIX hippocampus oligodendrocyte neuron nuclear factor I glia RRID: AB_1854421 cerebral cortex RRID: AB_1854424 NFIA NFIB RRID: AB_10608433 astrocyte microglia |
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SubjectTerms | Age Factors Animals astrocyte Astrocytes Cell Differentiation - physiology Cell lineage Cerebral cortex Cerebral Cortex - cytology Cerebral Cortex - growth & development Cerebral Cortex - metabolism Coagulation factors Corpus callosum cortex Dentate gyrus Ependymal cells Gene Expression Regulation, Developmental glia Granule cells Hippocampus Mice Mice, Inbred C57BL Mice, Inbred ICR Mice, Transgenic Microglia Neural stem cells Neuroglia - metabolism neuron Neuronal-glial interactions Neurons Neurons - metabolism NFI Transcription Factors - biosynthesis NFI Transcription Factors - genetics NFIA NFIB NFIX Nuclear factor I oligodendrocyte Oligodendrocytes Proteins Rodents RRID: AB_10608433 RRID: AB_10712361 RRID: AB_1854421 RRID: AB_1854424 Stem cell transplantation Transcription factors Ventricle (lateral) |
Title | Differential neuronal and glial expression of nuclear factor I proteins in the cerebral cortex of adult mice |
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