Back to Search
Start Over
Generation of a Nkx2.2Cre knock-in mouse line: Analysis of cell lineages in the central nervous system
- Source :
- Differentiation. 89:70-76
- Publication Year :
- 2015
- Publisher :
- Elsevier BV, 2015.
-
Abstract
- A Nkx2.2cre knock-in mutant mouse line was generated that on the appropriate reporter strain enables cell fate analysis of the Nkx2.2 cell lineage in the central nervous system and elsewhere. We here demonstrate that Nkx2.2 lineage-marked cells reside in the ventral p3 region along the entire length of the CNS and also in pancreas of mouse embryos. Nkx2.2+ progenitor cells develop into V3 interneurons in spinal cord and generate the branchio-visceral motor nuclei of cranial nerves in hindbrain. Nkx2.2+ cells in hindbrain also form serotonergic neurons and oligodendrocytes during later developmental stages. In mouse mutants lacking Nkx2.2 protein the neuronal progenitor cells in spinal cord are transformed to the distinct fate of somatic motor neurons including their axonal projections that exit the CNS ventrally and no longer cross the midline at the commissure. These data identify Nkx2.2 as key regulator to determine neuronal subtypes in the p3 domain of the central nervous system.
- Subjects :
- Central Nervous System
Cancer Research
Somatic cell
Central nervous system
Hindbrain
Cell fate determination
Biology
Serotonergic
Mice
stomatognathic system
medicine
Animals
Cell Lineage
Gene Knock-In Techniques
Progenitor cell
Molecular Biology
Body Patterning
Homeodomain Proteins
Motor Neurons
Genetics
Gene Expression Regulation, Developmental
Cell Differentiation
Cell Biology
Zebrafish Proteins
Commissure
Spinal cord
Cell biology
Homeobox Protein Nkx-2.2
medicine.anatomical_structure
Spinal Cord
nervous system
embryonic structures
cardiovascular system
Transcription Factors
Developmental Biology
Subjects
Details
- ISSN :
- 03014681
- Volume :
- 89
- Database :
- OpenAIRE
- Journal :
- Differentiation
- Accession number :
- edsair.doi.dedup.....6bab3ed00743b8447a80c588227096de
- Full Text :
- https://doi.org/10.1016/j.diff.2015.03.001