The

Müller glia, which act as the “stem” cell that gives rise to the rod precursors (Bernardos et al., 2007), express Sox2 and Pax6 (and Ascl1 after damage, see below), similar to the GBCs. From this overview, several common features of ongoing sensory cell production emerge. First, the sensory receptor cells are derived from what might be called a “persistent progenitor” or “sensory receptor cell precursor.” In both the olfactory epithelium and the retina of fish, the immediate precursor to the receptor neurons/rods is a cell that seems to have a more limited capacity for cell division than a true “stem cell.” The rod precursor of fish is particularly committed to generating rod photoreceptors, and the GBC of the olfactory epithelium can generate most, though not all, Olaparib purchase of the cell types in the sensory epithelium. These cells have some similarity to the immediate neuronal precursors found in the cerebral cortex or the progenitor/stem cells in the hippocampal and subventricular zone in that (1) they are restricted to generate specific subtypes of neurons and (2) their mitotic divisions do not occur GW3965 cost at the ventricular

surface (Hodge et al., 2008 and Pontious et al., 2008). Second, many of the genes expressed in normal development in the lineages leading to the differentiated sensory receptor cells are also expressed in the progenitors responsible for the genesis of these cells in mature sensory epithelia. Third, the progenitors/precursors in the mature epithelia coexist with differentiated, functioning sensory receptors, underscoring the fact that the maintenance of a “neurogenic” niche is not inconsistent with the environment of a mature neural tissue. Fourth, although the different systems have very different requirements Protein kinase N1 for the maintenance of sensory cell addition throughout life, the addition of new sensory receptors seems to serve a

very specific purpose in each system. Lastly, although the rate of new cell addition in the different systems varies considerably, where the olfactory epithelium generates new sensory receptors at a much higher rate than the other epithelia, the production of new cells appears to be under tight regulation, producing precisely the cell types necessary for maintenance and growth or regeneration of these structures. Before delving into regeneration in the different sensory epithelia, it would be worthwhile to provide a development framework in which to understand the molecular underpinnings of and constraints on regeneration. The development of the specialized sensory organs share many mechanisms with one another and other regions of the nervous system (Figure 3). Paired-homeodomain (Pax), bHLH proneural/neural differentiation, SRY-related HMG-box (Sox), and homeodomain transcription factors are all necessary for these sensory organs. Signaling factors and their receptors, including BMP, FGF, Shh, Wnt, and Dll/Notch, are also important in the development of these systems.