Novel lines of Pax6-/- embryonic stem cells exhibit reduced neurogenic capacity without loss of viability

Autor: Tomasz J. Nowakowski, David Price, John O. Mason, Michael Molinek, Jane Quinn
Jazyk: angličtina
Rok vydání: 2010
Předmět:
endocrine system
Time Factors
PAX6 Transcription Factor
Cell Survival
Cellular differentiation
Neurogenesis
Mice
Transgenic
Embryoid body
Biology
Hippocampus
Cell Line
lcsh:RC321-571
03 medical and health sciences
Chimera (genetics)
Mice
Cellular and Molecular Neuroscience
0302 clinical medicine
Research article
Animals
Paired Box Transcription Factors
Eye Proteins
lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry
Embryonic Stem Cells
030304 developmental biology
Cell Proliferation
Cerebral Cortex
Homeodomain Proteins
Neurons
0303 health sciences
Chimera
General Neuroscience
lcsh:QP351-495
Cell Differentiation
Embryonic stem cell
Molecular biology
eye diseases
Repressor Proteins
P19 cell
Phenotype
lcsh:Neurophysiology and neuropsychology
nervous system
Cell culture
sense organs
Stem cell
030217 neurology & neurosurgery
Zdroj: BMC Neuroscience, Vol 11, Iss 1, p 26 (2010)
Quinn, J C, Molinek, M, Nowakowski, T J, Mason, J O & Price, D J 2010, ' Novel lines of Pax6-/-embryonic stem cells exhibit reduced neurogenic capacity without loss of viability ', BMC Neuroscience, vol. 11, 26 . https://doi.org/10.1186/1471-2202-11-26
BMC Neuroscience
ISSN: 1471-2202
Popis: Background Embryonic stem (ES) cells can differentiate into all cell types and have been used extensively to study factors affecting neuronal differentiation. ES cells containing mutations in known genes have the potential to provide useful in vitro models for the study of gene function during neuronal differentiation. Recently, mouse ES cell lines lacking the neurogenic transcription factor Pax6 were reported; neurons derived from these Pax6-/- ES cells died rapidly after neuronal differentiation in vitro. Results Here we report the derivation of new lines of Pax6-/- ES cells and the assessment of their ability to survive and differentiate both in vitro and in vivo. Neurons derived from our new Pax6-/- lines were viable and continued to elaborate processes in culture under conditions that resulted in the death of neurons derived from previously reported Pax6-/- ES cell lines. The new lines of Pax6-/-ES cells showed reduced neurogenic potential, mimicking the effects of loss of Pax6 in vivo. We used our new lines to generate Pax6-/- ↔ Pax6+/+ chimeras in which the mutant cells survived and displayed the same phenotypes as Pax6-/- cells in Pax6-/- ↔ Pax6+/+ chimeras made by embryo aggregation. Conclusions We suggest that loss of Pax6 from ES cells reduces their neurogenic capacity but does not necessarily result in the death of derived neurons. We offer these new lines as additional tools for those interested in the generation of chimeras and the analysis of in vitro ES cell models of Pax6 function during neuronal differentiation, embryonic and postnatal development.
Databáze: OpenAIRE
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