And in terms of papers like Spalding et al., 2013 which "assessed the generation of hippocampal cells in humans by measuring the concentration of nuclear-bomb-test-derived 14C in genomic DNA"?
https://www.sciencedirect.com/science/article/pii/S009286741...
"A study using 14C birthdating on sorted NeuN+ nuclei suggested that hundreds of new neurons are generated per day in the adult human hippocampus, with little decline with age. The results obtained from this method differ from the data presented here and other histology studies that show a sharp decline in markers of newly formed neurons during early postnatal development. Birthdating with 14C relies on the isolation of neuronal nuclei using NeuN antibodies, but subpopulations of oligodendrocytes and microglia can also express NeuN. 14C could also possibly become incorporated into DNA through methylation or DNA repair independent of cell division, processes that have been shown to occur at higher rates in the hippocampus. The proposed addition of new neurons to the adult caudate nucleus using this method is not supported by other work in the human or BrdU labeling in adult macaques. The 14C method is an innovative approach to perform birthdating in postmortem human samples, but it has not been validated in animal studies."
In the cortex at least there have been reports of DCX+ NCAM+ cells that are arrested in an immature state, meaning they are not necessarily newly generated, just stuck in "standby" mode.
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Probably. But to clarify you think something besides immature GNs in the granular zone expresses DCX and PSA-NCAM but not NeuN?
I have my idea; I just want to hear yours.
And in terms of papers like Spalding et al., 2013 which "assessed the generation of hippocampal cells in humans by measuring the concentration of nuclear-bomb-test-derived 14C in genomic DNA"? https://www.sciencedirect.com/science/article/pii/S009286741...
The original study https://www.nature.com/articles/nature25975 that prompted the SSC article has an interesting discussion of this result in their supplement:
"A study using 14C birthdating on sorted NeuN+ nuclei suggested that hundreds of new neurons are generated per day in the adult human hippocampus, with little decline with age. The results obtained from this method differ from the data presented here and other histology studies that show a sharp decline in markers of newly formed neurons during early postnatal development. Birthdating with 14C relies on the isolation of neuronal nuclei using NeuN antibodies, but subpopulations of oligodendrocytes and microglia can also express NeuN. 14C could also possibly become incorporated into DNA through methylation or DNA repair independent of cell division, processes that have been shown to occur at higher rates in the hippocampus. The proposed addition of new neurons to the adult caudate nucleus using this method is not supported by other work in the human or BrdU labeling in adult macaques. The 14C method is an innovative approach to perform birthdating in postmortem human samples, but it has not been validated in animal studies."
In the cortex at least there have been reports of DCX+ NCAM+ cells that are arrested in an immature state, meaning they are not necessarily newly generated, just stuck in "standby" mode.
Why don't you go for it? I'd like to hear.
glial cells moonlighting, by expressing the molecular marker signature of young neurons.