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For a 10 sec guide to cell labeling with Brd U and phenotypic markers, see here.

The previous timecourses are all well and good but sheer numbers of cells say nothing about whether the new neurons actually work.

The result of these many hours of work will either be a) that the purpose of adult neurogenesis will become immediately clear, or b) that we’ll all have some fancy collages to pin on our bulletin boards and look intelligent. The survival timecourse answers the questions: How many new neurons are born?

Where are they born and where do they end up, anatomically?

³H-thymidine (old school), Brd U (tried and true – example), or a GFP-expressing retrovirus (new school).

Survival timecourses are typically performed by injecting animals with a mitotic marker that will label new neurons as they’re being born, e.g.By examining the same thing at multiple time points, each study inherently has a lot of controls.If you take a single time point out of some of these studies, say the % of new neurons that have excitatory glutamatergic inputs at 14 days-old in Esposito 2005 and Ge 2006, you might wonder, who’s right here? I curious as to why they differ but I still trust both of these studies and refer to them often because, within their respective timecourses, both 14-day data points make sense and, across studies, the 2 timecourses themselves do generally agree, even if they are slightly shifted.I’ve ordered the data roughly chronologically and have included the first author’s name and publication year so you can read deeper, if needed.Indeed, if you know these studies already, a brief look at the graphs will bring back the take home message.

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