Odorants Selectively Activate Distinct G Protein Subtypes in Olfactory Cilia
Chemoelectrical signal transduction in olfactory neurons appears to involve intracellular reaction cascades mediated by heterotrimeric GTP-binding proteins. In this study attempts were made to identify the G protein subtype(s) in olfactory cilia that are activated by the primary (odorant) signal. An...
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Veröffentlicht in: | The Journal of biological chemistry 1998-07, Vol.273 (27), p.16669-16677 |
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Sprache: | eng |
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Zusammenfassung: | Chemoelectrical signal transduction in olfactory neurons appears to involve intracellular reaction cascades mediated by heterotrimeric
GTP-binding proteins. In this study attempts were made to identify the G protein subtype(s) in olfactory cilia that are activated
by the primary (odorant) signal. Antibodies directed against the α subunits of distinct G protein subtypes interfered specifically
with second messenger reponses elicited by defined subsets of odorants; odor-induced cAMP-formation was attenuated by Gα s antibodies, whereas Gα o antibodies blocked odor-induced inositol 1,4,5-trisphosphate (IP 3 ) formation. Activation-dependent photolabeling of Gα subunits with [α- 32 P]GTP azidoanilide followed by immunoprecipitation using subtype-specific antibodies enabled identification of particular
individual G protein subtypes that were activated upon stimulation of isolated olfactory cilia by chemically distinct odorants.
For example odorants that elicited a cAMP response resulted in labeling of a Gα s -like protein, whereas odorants that elicited an IP 3 response led to the labeling of a Gα o -like protein. Since odorant-induced IP 3 formation was also blocked by G β antibodies, activation of olfactory phospholipase C might be mediated by βγ subunits of a G o -like G protein. These results indicate that different subsets of odorants selectively trigger distinct reaction cascades
and provide evidence for dual transduction pathways in olfactory signaling. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.273.27.16669 |