tec-1 kinase negatively regulates regenerative neurogenesis in planarians.
Alexander KargeNicolle A BonarScott WoodChristian P PetersenPublished in: eLife (2020)
Negative regulators of adult neurogenesis are of particular interest as targets to enhance neuronal repair, but few have yet been identified. Planarians can regenerate their entire CNS using pluripotent adult stem cells, and this process is robustly regulated to ensure that new neurons are produced in proper abundance. Using a high-throughput pipeline to quantify brain chemosensory neurons, we identify the conserved tyrosine kinase tec-1 as a negative regulator of planarian neuronal regeneration. tec-1RNAi increased the abundance of several CNS and PNS neuron subtypes regenerated or maintained through homeostasis, without affecting body patterning or non-neural cells. Experiments using TUNEL, BrdU, progenitor labeling, and stem cell elimination during regeneration indicate tec-1 limits the survival of newly differentiated neurons. In vertebrates, the Tec kinase family has been studied extensively for roles in immune function, and our results identify a novel role for tec-1 as negative regulator of planarian adult neurogenesis.
Keyphrases
- stem cells
- tyrosine kinase
- cerebral ischemia
- transcription factor
- blood brain barrier
- spinal cord
- high throughput
- epidermal growth factor receptor
- cell therapy
- neural stem cells
- subarachnoid hemorrhage
- induced apoptosis
- multidrug resistant
- mesenchymal stem cells
- antibiotic resistance genes
- brain injury
- protein kinase
- cell cycle arrest
- cell proliferation
- oxidative stress
- white matter
- signaling pathway
- spinal cord injury
- bone marrow
- resting state
- young adults