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PMID: 11301001 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Pax6 is required for the multipotent state of retinal progenitor cells.

Cell ·Vol. 105 ·No. 1 ·2001-04-06 ·Pages 43-55

Marquardt T, Ashery-Padan R, Andrejewski N, Scardigli R, Guillemot F, Gruss P

Abstract

The molecular mechanisms mediating the retinogenic potential of multipotent retinal progenitor cells (RPCs) are poorly defined. Prior to initiating retinogenesis, RPCs express a limited set of transcription factors implicated in the evolutionary ancient genetic network that initiates eye development. We elucidated the function of one of these factors, Pax6, in the RPCs of the intact developing eye by conditional gene targeting. Upon Pax6 inactivation, the potential of RPCs becomes entirely restricted to only one of the cell fates normally available to RPCs, resulting in the exclusive generation of amacrine interneurons. Our findings demonstrate furthermore that Pax6 directly controls the transcriptional activation of retinogenic bHLH factors that bias subsets of RPCs toward the different retinal cell fates, thereby mediating the full retinogenic potential of RPCs.

MeSH Terms
Animals Cell Line Cell Lineage Chick Embryo Clone Cells/cytology Eye Proteins Gene Targeting Helix-Loop-Helix Motifs Homeodomain Proteins/genetics,metabolism Interneurons/cytology,metabolism Membrane Proteins/metabolism Mice Mice, Transgenic Morphogenesis Neurotransmitter Agents/metabolism PAX6 Transcription Factor Paired Box Transcription Factors Phenotype Qa-SNARE Proteins Repressor Proteins Retina/cytology,embryology,metabolism Stem Cells/cytology,metabolism Transcription Factors/metabolism Transcriptional Activation
Chemicals
Eye Proteins Homeodomain Proteins Membrane Proteins Neurotransmitter Agents PAX6 Transcription Factor Paired Box Transcription Factors Pax6 protein, mouse Qa-SNARE Proteins Repressor Proteins Transcription Factors
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Marquardt T
Max-Planck-Institute of Biophysical Chemistry, Department of Molecular Cell Biology, Am Fassberg 11, D-37077, Göttingen, Germany.
Ashery-Padan R
Andrejewski N
Scardigli R
Guillemot F
Gruss P
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
2001-04-06
Pages
43-55
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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