Abstract
In mammals, taste buds typically contain 50-100 tightly packed taste-receptor cells (TRCs), representing all five basic qualities: Sweet, sour, bitter, salty and umami. Notably, mature taste cells have life spans of only 5-20 days and, consequently, are constantly replenished by differentiation of taste stem cells. Given the importance of establishing and maintaining appropriate connectivity between TRCs and their partner ganglion neurons (that is, ensuring that a labelled line from sweet TRCs connects to sweet neurons, bitter TRCs to bitter neurons, sour to sour, and so on), we examined how new connections are specified to retain fidelity of signal transmission. Here we show that bitter and sweet TRCs provide instructive signals to bitter and sweet target neurons via different guidance molecules (SEMA3A and SEMA7A). We demonstrate that targeted expression of SEMA3A or SEMA7A in different classes of TRCs produces peripheral taste systems with miswired sweet or bitter cells. Indeed, we engineered mice with bitter neurons that now responded to sweet tastants, sweet neurons that responded to bitter or sweet neurons responding to sour stimuli. Together, these results uncover the basic logic of the wiring of the taste system at the periphery, and illustrate how a labelled-line sensory circuit preserves signalling integrity despite rapid and stochastic turnover of receptor cells.
Original language | English (US) |
---|---|
Pages (from-to) | 330-333 |
Number of pages | 4 |
Journal | Nature |
Volume | 548 |
Issue number | 7667 |
DOIs | |
State | Published - Aug 17 2017 |
Funding
Acknowledgements We thank T. Yagi for providing the floxed Sema3a mice, R. Barretto and D. Yarmolinsky for help with in vivo imaging and analysis, and Z. Wu, I. Schieren and S. O’Keeffe for advice and expert technical support. We also thank N. Balaskas and the members of the Zuker laboratory for helpful comments and suggestions. Research reported in this publication was supported by the National Institute On Drug Abuse of the National Institutes of Health under Award Number R01DA035025 (C.S.Z.) and in part by the Intramural Research Program of the NIH, NIDCR (N.J.P.R.). L.J.M. was an HHMI Fellow of the Jane Coffin Childs Memorial Fund. C.S.Z. is an investigator of the Howard Hughes Medical Institute and a Senior Fellow at Janelia Farm Research Campus.
ASJC Scopus subject areas
- General