Regulation of hippocampal postnatal and adult neurogenesis by adenosine A2A receptor: Interaction with brain-derived neurotrophic factor.
Filipa F RibeiroFilipa FerreiraRui S RodriguesRita SoaresDiogo M PedroMarta Duarte-SamartinhoRita I AroeiraElisabete FerreiroJorge ValeroSusana SoláHelena MiraAna M SebastiãoSara XapelliPublished in: Stem cells (Dayton, Ohio) (2021)
Adenosine A2A receptor (A2A R) activation modulates several brain processes, ranging from neuronal maturation to synaptic plasticity. Most of these actions occur through the modulation of the actions of the neurotrophin brain-derived neurotrophic factor (BDNF). In this work, we studied the role of A2A Rs in regulating postnatal and adult neurogenesis in the rat hippocampal dentate gyrus (DG). Here, we show that A2A R activation with CGS 21680 promoted neural stem cell self-renewal, protected committed neuronal cells from cell death and contributed to a higher density of immature and mature neuronal cells, particularly glutamatergic neurons. Moreover, A2A R endogenous activation was found to be essential for BDNF-mediated increase in cell proliferation and neuronal differentiation. Our findings contribute to further understand the role of adenosinergic signaling in the brain and may have an impact in the development of strategies for brain repair under pathological conditions.
Keyphrases
- cerebral ischemia
- subarachnoid hemorrhage
- blood brain barrier
- brain injury
- cell death
- stem cells
- cell proliferation
- cell cycle arrest
- preterm infants
- induced apoptosis
- resting state
- oxidative stress
- spinal cord
- pi k akt
- spinal cord injury
- protein kinase
- cell cycle
- signaling pathway
- childhood cancer
- bone marrow
- endoplasmic reticulum stress