It will therefore be necessary to characterize more subtypes

of early RPCs to ensure that some share identical lineages. In the stochastic model, a given RPC does not have a predefined pattern of mitosis or progeny fate specification. Its lineage is the result of random choices of cell fates made at each cell division by the progeny. It might be difficult to imagine that stochastic lineages from progenitor cells can generate homeostatic tissues with consistent size and cell-type composition. However, studies in other stem cell model systems suggest that this is possible. For example, quantitative analysis showed surprising stochasticity in the progeny of stem cells in self-renewing adult tissues such as the murine epidermis and intestinal epithelium (reviewed in Simons and Clevers, 2011). In these systems, the stem

cells do not follow the classic asymmetrical self-renewing division mode. Instead, they usually divide symmetrically and the resultant selleck kinase inhibitor progeny make their own stochastic choices to stay in the stem cell fate or to move toward a differentiated cell fate. Although this stochasticity results in great variation in the size, cell-type composition, and dynamics of individual stem cell clones, modeling showed that the various cell types can be produced in the correct proportion, while Crenolanib supplier tissue homeostasis can be well maintained at the population level (Simons and Clevers, 2011). Which model better fits the actual vertebrate retinogenesis scenario? Statistical analysis and mathematical modeling of data from in vitro cell culture and time-lapse microscopy had unveiled similar stochasticity in late rat RPCs (Gomes et al., 2011), which choose to divide with three possible outcomes with a specific proportion of each division mode at a given stage of development. These modes give rise to (1) two daughter progenitor cells (PP division), resulting in expansion of the progenitor population; (2) one progenitor daughter cell and one differentiating

daughter cell (self-renewing PD division), which is a stem cell mode that produces neurons with a linear amplification; and (3) two terminally differentiated daughter cells (DD division), a mode that ends the lineage (Figure 1B). The variability in the cell-type birth order and the inability to identify a large Histone demethylase number of identical lineages also showed that the system might rely on stochastic choices of cell fates. However, there were still important questions remaining. Is the stochastic model true in vivo and is it applicable to earlier-stage RPCs? The paper by He et al. (2012) addresses these questions in zebrafish by tracing RPC lineages in vivo in the developing retina. Zebrafish are an excellent model organism for this purpose as their retinas are easily accessible for manipulation and allow live imaging even at early retinogenesis stages. Using photoconvertible fluorescent protein expression in clones induced by heat shock, He et al.