The evidence that manipulating both Wnt and notch signalling has the potential to regenerate hair cells while preserving supporting cell population continues to grow. The caveat is that much of this work is in very young animals so it remains to be seen what translates to adults.
A new paper by Albert Edge and Fuxin Shi and colleagues (http://www.jneurosci.org/content/36/36/9479.abstract) suggests that there is a threshold level of Wnt signalling required for regeneration and that inhibiting notch signalling increases the size of the effect.
SIGNIFICANCE STATEMENT Sensory HCs of the inner ear do not regenerate in the adult, and their loss is a major cause of deafness. We found that HCs regenerated spontaneously in the newborn mouse after diphtheria toxin (DT)-induced, but not neomycin-induced, HC death. Regeneration depended on activation of Wnt signaling, and regeneration in DT-treated ears correlated to a higher level of Wnt activation than occurred in nonregenerating neomycin-treated ears. This is significant because insufficient regeneration caused by a failure to reach a threshold level of signaling, if true in the adult, has the potential to be exploited for development of clinical approaches for the treatment of deafness caused by HC loss.
This comes on the heels of a series of papers by Huwei Li and colleagues that explore the interactions of Wnt and Notch signalling:
http://www.jneurosci.org/content/36/33/8734.abstract
http://www.nature.com/articles/srep29418
http://www.pnas.org/content/112/1/166.long
Based on earlier publications, Li was almost certainly a postdoc in Heller's lab at Harvard when Heller was at Harvard; Li's lab is quite prolific in the last couple of years.
This is promising, but it is not clear how perfectly the multiple pathways must be understand (and there are more then two - Edge has a new paper about another pathway regulating Atoh1: http://www.ncbi.nlm.nih.gov/pubmed/27542412).
A new paper by Albert Edge and Fuxin Shi and colleagues (http://www.jneurosci.org/content/36/36/9479.abstract) suggests that there is a threshold level of Wnt signalling required for regeneration and that inhibiting notch signalling increases the size of the effect.
SIGNIFICANCE STATEMENT Sensory HCs of the inner ear do not regenerate in the adult, and their loss is a major cause of deafness. We found that HCs regenerated spontaneously in the newborn mouse after diphtheria toxin (DT)-induced, but not neomycin-induced, HC death. Regeneration depended on activation of Wnt signaling, and regeneration in DT-treated ears correlated to a higher level of Wnt activation than occurred in nonregenerating neomycin-treated ears. This is significant because insufficient regeneration caused by a failure to reach a threshold level of signaling, if true in the adult, has the potential to be exploited for development of clinical approaches for the treatment of deafness caused by HC loss.
This comes on the heels of a series of papers by Huwei Li and colleagues that explore the interactions of Wnt and Notch signalling:
http://www.jneurosci.org/content/36/33/8734.abstract
http://www.nature.com/articles/srep29418
http://www.pnas.org/content/112/1/166.long
Based on earlier publications, Li was almost certainly a postdoc in Heller's lab at Harvard when Heller was at Harvard; Li's lab is quite prolific in the last couple of years.
This is promising, but it is not clear how perfectly the multiple pathways must be understand (and there are more then two - Edge has a new paper about another pathway regulating Atoh1: http://www.ncbi.nlm.nih.gov/pubmed/27542412).