Literature DB >> 19686101

The role of foxg1 in the development of neural stem cells of the olfactory epithelium.

Shimako Kawauchi1, Rosaysela Santos, Joon Kim, Piper L W Hollenbeck, Richard C Murray, Anne L Calof.   

Abstract

The olfactory epithelium (OE) of the mouse is an excellent model system for studying principles of neural stem cell biology because of its well-defined neuronal lineage and its ability to regenerate throughout life. To approach the molecular mechanisms of stem cell regulation in the OE, we have focused on Foxg1, also known as brain factor 1, which is a member of the Forkhead transcription factor family. Foxg1(-/-) mice show major defects in the OE at birth, suggesting that Foxg1 plays an important role in OE development. We find that Foxg1 is expressed in cells within the basal compartment of the OE, the location where OE stem and progenitor cells are known to reside. Since FoxG1 is known to regulate proliferation of neuronal progenitor cells during telencephalon development, we performed bromodeoxyuridine pulse-chase labeling of Sox2-expressing neural stem cells during primary OE neurogenesis. We found the percentage of Sox2-expressing cells that retained bromodeoxyuridine was twice as high in Foxg1(-/-) OE cells as in the wild type, suggesting that these cells are delayed and/or halted in their development in the absence of Foxg1. Our findings suggest that the proliferation and/or subsequent differentiation of Sox2-expressing neural stem cells in the OE is regulated by Foxg1.

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Year:  2009        PMID: 19686101      PMCID: PMC2878634          DOI: 10.1111/j.1749-6632.2009.04372.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  52 in total

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2.  BMPs inhibit neurogenesis by a mechanism involving degradation of a transcription factor.

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Journal:  Nat Neurosci       Date:  1999-04       Impact factor: 24.884

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4.  Globose basal cells are required for reconstitution of olfactory epithelium after methyl bromide lesion.

Authors:  Woochan Jang; Steven L Youngentob; James E Schwob
Journal:  J Comp Neurol       Date:  2003-05-19       Impact factor: 3.215

5.  Progenitor cells of the olfactory receptor neuron lineage.

Authors:  Anne L Calof; Alexandre Bonnin; Candice Crocker; Shimako Kawauchi; Richard C Murray; Jianyong Shou; Hsiao-Huei Wu
Journal:  Microsc Res Tech       Date:  2002-08-01       Impact factor: 2.769

Review 6.  Forkhead transcription factors: key players in development and metabolism.

Authors:  Peter Carlsson; Margit Mahlapuu
Journal:  Dev Biol       Date:  2002-10-01       Impact factor: 3.582

7.  Olfactory marker protein during ontogeny: immunohistochemical localization.

Authors:  A I Farbman; F L Margolis
Journal:  Dev Biol       Date:  1980-01       Impact factor: 3.582

8.  Adult olfactory epithelium contains multipotent progenitors that give rise to neurons and non-neural cells.

Authors:  J M Huard; S L Youngentob; B J Goldstein; M B Luskin; J E Schwob
Journal:  J Comp Neurol       Date:  1998-11-02       Impact factor: 3.215

9.  Comparative expression of the mouse Sox1, Sox2 and Sox3 genes from pre-gastrulation to early somite stages.

Authors:  H B Wood; V Episkopou
Journal:  Mech Dev       Date:  1999-08       Impact factor: 1.882

10.  Multipotent cell lineages in early mouse development depend on SOX2 function.

Authors:  Ariel A Avilion; Silvia K Nicolis; Larysa H Pevny; Lidia Perez; Nigel Vivian; Robin Lovell-Badge
Journal:  Genes Dev       Date:  2003-01-01       Impact factor: 11.361

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  10 in total

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Review 3.  Transcriptional and Epigenetic Control of Mammalian Olfactory Epithelium Development.

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Review 5.  Translational potential of olfactory mucosa for the study of neuropsychiatric illness.

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6.  The Dlx5 and Foxg1 transcription factors, linked via miRNA-9 and -200, are required for the development of the olfactory and GnRH system.

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Review 7.  Sensational placodes: neurogenesis in the otic and olfactory systems.

Authors:  Esther C Maier; Ankur Saxena; Berta Alsina; Marianne E Bronner; Tanya T Whitfield
Journal:  Dev Biol       Date:  2014-02-06       Impact factor: 3.582

8.  Knockdown of Foxg1 in supporting cells increases the trans-differentiation of supporting cells into hair cells in the neonatal mouse cochlea.

Authors:  Shasha Zhang; Yuan Zhang; Ying Dong; Lingna Guo; Zhong Zhang; Buwei Shao; Jieyu Qi; Han Zhou; Weijie Zhu; Xiaoqian Yan; Guodong Hong; Liyan Zhang; Xiaoli Zhang; Mingliang Tang; Chunjie Zhao; Xia Gao; Renjie Chai
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9.  Hypoxia-Responsive Subtype Cells Differentiate Into Neurons in the Brain of Zebrafish Embryos Exposed to Hypoxic Stress.

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10.  Knockdown of Foxg1 in Sox9+ supporting cells increases the trans-differentiation of supporting cells into hair cells in the neonatal mouse utricle.

Authors:  Yuan Zhang; Shasha Zhang; Zhonghong Zhang; Ying Dong; Xiangyu Ma; Ruiying Qiang; Yin Chen; Xia Gao; Chunjie Zhao; Fangyi Chen; Shuangba He; Renjie Chai
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  10 in total

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