Abstract
Marking replicating DNA with multiple labels presents the possibility of revealing new features and mechanisms of DNA synthesis and cell division; however, progression beyond double labeling has been hampered by cross-reactivity of label detection and scarcity of appropriate labels. Here, we present a method for triple S-phase labeling of the dividing cells, with a fourth label used to mark cells actively engaged in cell-cycle progression (e.g., using Ki67) or to phenotype the dividing cells or their progeny (e.g., using a GFP-expressing lineage reporter transgene). We apply this method to determine the parameters of neural stem cell division in the adult brain, to birth date up to four cohorts of dividing cells, and to reveal patterns of stem cell division in non-neural tissues. In this article, Enikolopov and colleagues describe a method for triple S-phase labeling of stem cells, with an additional channel used to phenotype the cells or to add the fourth marker of cell division. They demonstrate the method's utility for birth dating multiple stem cell populations and for revealing patterns of stem cell division in the brain, testis, and intestine.
| Original language | English |
|---|---|
| Pages (from-to) | 615-626 |
| Number of pages | 12 |
| Journal | Stem Cell Reports |
| Volume | 10 |
| Issue number | 2 |
| DOIs | |
| State | Published - Feb 13 2018 |
Keywords
- S-phase labeling
- adult neurogenesis
- cell cycle
- dentate gyrus
- intestinal stem cells
- neural stem cells
- proliferation
- stem cell maintenance
- subventricular zone
- thymidine analogs
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