Hartman Institute for Therapeutic Organ Regeneration

Identification of positionally distinct astrocyte subtypes whose identities are specified by a homeodomain code.

TitleIdentification of positionally distinct astrocyte subtypes whose identities are specified by a homeodomain code.
Publication TypeJournal Article
Year of Publication2008
AuthorsHochstim C, Deneen B, Lukaszewicz A, Zhou Q, Anderson DJ
JournalCell
Volume133
Issue3
Pagination510-22
Date Published2008 May 02
ISSN1097-4172
KeywordsAnimals, Astrocytes, Cell Adhesion Molecules, Neuronal, Chick Embryo, Embryo, Mammalian, Extracellular Matrix Proteins, Eye Proteins, Gene Expression, Homeodomain Proteins, Mice, Nerve Tissue Proteins, Paired Box Transcription Factors, PAX6 Transcription Factor, Reelin Protein, Repressor Proteins, Serine Endopeptidases, Spinal Cord, Stem Cells, Transcription, Genetic
Abstract

<p>Astrocytes constitute the most abundant cell type in the central nervous system (CNS) and play diverse functional roles, but the ontogenetic origins of this phenotypic diversity are poorly understood. We have investigated whether positional identity, a fundamental organizing principle governing the generation of neuronal subtype diversity, is also relevant to astrocyte diversification. We identified three positionally distinct subtypes of white-matter astrocytes (WMA) in the spinal cord, which can be distinguished by the combinatorial expression of Reelin and Slit1. These astrocyte subtypes derive from progenitor domains expressing the homeodomain transcription factors Pax6 and Nkx6.1, respectively. Loss- and gain-of-function experiments indicate that the positional identity of these astrocyte subtypes is controlled by Pax6 and Nkx6.1 in a combinatorial manner. Thus, positional identity is an organizing principle underlying astrocyte, as well as neuronal, subtype diversification and is controlled by a homeodomain transcriptional code whose elements are reutilized following the specification of neuronal identity earlier in development.</p>

DOI10.1016/j.cell.2008.02.046
Alternate JournalCell
PubMed ID18455991
PubMed Central IDPMC2394859
Grant ListR01 NS023476 / NS / NINDS NIH HHS / United States
R01 NS023476-22 / NS / NINDS NIH HHS / United States
/ HHMI / Howard Hughes Medical Institute / United States
1R01-NS23476 / NS / NINDS NIH HHS / United States

Weill Cornell Medicine
Hartman Institute for Therapeutic Organ Regeneration
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