Coupling of excitation and neurogenesis in neural stem/progenitor cells
View Patent ↗Coupling of excitation to neurogenesis in proliferating post-natal NPCs is demonstrated in vitro and in vivo. Neurogenesis is potently enhanced by excitatory stimuli, and involves Ca v 1.2/1.3 channels and NMDA receptors. These Ca 2+ influx pathways are located on the proliferating NPCs, allowing them to directly sense and process excitatory stimuli. Excitation increases the fraction of NPC progeny that are neurons, and increases total neuron number. Signaling in this pathway leads to rapid induction of a proneural gene expression pattern involving the bHLH genes HES1, Id2, and NeuroD, and the resulting cells become fully functional neurons defined by neuronal morphology, expression of neuronal structural proteins, expression of neuronal TTX-sensitive voltage gated Na + channels, and synaptic incorporation into active neural circuits.
1. A method of promoting or inhibiting neurogenesis, the method comprising the step of directly exciting neural progenitor cells in a rat with a therapeutic amount of an agent that directly acts on one or both of voltage-activated gated Ca 2+ channels or NMDA receptors, wherein when said agent is an agonist of said voltage-activated gated Ca 2+ channels or NMDA receptors neurogenesis is promoted in said neural progenitor cells, and wherein when said agent is an antagonist of said voltage-activated gated Ca 2+ channels or NMDA receptors neurogenesis is inhibited in said neural progenitor cells.
2. A method of promoting or inhibiting neurogenesis, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that directly acts on one or both of voltage-activated gated Ca 2+ channels or NMDA receptors, wherein when said agent is an agonist of said voltage-activated gated Ca 2+ channels or NMDA receptors neurogenesis is promoted in said neural progenitor cells, and wherein when said agent is an antagonist of said voltage-activated gated Ca 2+ channels or NMDA receptors neurogenesis is inhibited in said neural progenitor cells wherein said neural progenitor cells are in vitro.
3. The method according to claim 2 , wherein said neural progenitor cells are neonatal cells.
4. The method according to claim 2 , wherein said neural progenitor cells are adult cells.
5. The method according to claim 2 , wherein said agent is the alteration of ionic concentrations in an environment of said neural progenitor cells.
6. A method of promoting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific agonist of Ca v 1.2/1.3 channels, wherein generation of neurons from neural progenitor cells is increased in said neural progenitor cells.
7. A method of promoting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific agonist of Ca v 1.2/1.3 channels, wherein generation of neurons from neural progenitor cells is increased in said neural progenitor cells, wherein said agonist is selected from FPL 64176 and BAY K-8644.
8. A method of promoting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific agonist of NMDA-R, wherein generation of neurons from neural progenitor cells is increased in said neural progenitor cells.
9. A method of promoting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific agonist of NMDA-R, wherein generation of neurons from neural progenitor cells is increased in said neural progenitor cells, wherein said agonist is selected from GIyT1 inhibitor N[3-(4-fluorophenyl)-3-(4′-phenylphenoxy)propyl]sarcosine (NFPS); NMDA; (R)-(+)-HA-966; glycine; D-serine; (RS)-(Tetrazol-5-yl)glycine, and trans-ACBD.
10. A method of inhibiting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific antagonist of Ca v 1.2/1.3 channels, wherein generation of neurons from neural progenitor cells is decreased in said neural progenitor cells.
11. A method of inhibiting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific antagonist of Ca v 1.2/1.3 channels, wherein generation of neurons from neural progenitor cells is decreased in said neural progenitor cells, wherein said antagonist is selected from diltiazem, verapamil, nifedipine, nimodipine, and dimemorfan (3-methyl-N-methylmorphinan).
12. A method of inhibiting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific antagonist of NMDA-R, wherein generation of neurons from neural progenitor cells is decreased in said neural progenitor cells.
13. A method of inhibiting neurogenesis in vitro, the method comprising the step of directly exciting neural progenitor cells with a therapeutic amount of an agent that is a specific antagonist of NMDA-R, wherein generation of neurons from neural progenitor cells is decreased in said neural progenitor cells, wherein said antagonist is selected from D-AP5; MK801, memantine, CGP 39551; SDZ 220-581; CGP 78608 hydrochloride; and 5,7-Dichlorokynurenic acid.