XB-ART-46521
PLoS One
2012 Jan 01;712:e53097. doi: 10.1371/journal.pone.0053097.
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Amino acid- vs. peptide-odorants: responses of individual olfactory receptor neurons in an aquatic species.
Hassenklöver T
,
Pallesen LP
,
Schild D
,
Manzini I
.
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Amino acids are widely used waterborne olfactory stimuli proposed to serve as cues in the search for food. In natural waters the main source of amino acids is the decomposition of proteins. But this process also produces a variety of small peptides as intermediate cleavage products. In the present study we tested whether amino acids actually are the natural and adequate stimuli for the olfactory receptors they bind to. Alternatively, these olfactory receptors could be peptide receptors which also bind amino acids though at lower affinity. Employing calcium imaging in acute slices of the main olfactory epithelium of the fully aquatic larvae of Xenopus laevis we show that amino acids, and not peptides, are more effective waterborne odorants.
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Figure 2. Response profiles of ORNs to amino acid and peptide stimulation.(A) Relative number of amino acid-sensitive ORNs reacting to individual amino acids (200 µM) or at least to one of the thirteen tested peptides. Only a fraction of amino acid-responsive ORNs also responded to group I peptides (1 mM, 12 of 42 ORNs in four slices) or group II peptides (200 µM, 6 of 28 ORNs in four slices). The fraction of ORNs sensitive to group I peptides did not differ from the fraction of ORNs sensitive to group II peptides. (B) Response matrix of all peptide-sensitive ORNs to the applied stimuli (green, response to applied stimulus; red, no response; grey, not tested; applied peptide concentration: ORN #1â#12, 1 mM; ORN #13â#21, 5 mM; ORN #22â#24, 10 mM; ORN #25â#31, 200 µM). [AA mix: amino acid mixture, AA: amino acids, Arg: L-arginine, Met: L-methionine, Lys: L-lysine, Gly: glycine, Pep I: group I peptides, Pep II: group II peptides]. | |
Figure 3. Peptide stimulation evokes calcium transients with lower maximum amplitude than stimulation with amino acids.(A) The maximum amplitude of [Ca2+]i increases upon peptide application (green, group I, 1 mM; orange, group II, 200 µM) is much lower than upon application of amino acids (200 µM; number of responses averaged: L-arginyl-L-methionine (Arg-Met), 2; L-arginyl-L-methionyl-L-arginine (Arg-Met-Arg), 4; L-methionyl-L-arginyl-L-methionine (Met-Arg-Met), 9; L-methionyl-L-arginine (Met-Arg), 9; L-arginyl-L-lysine (Arg-Lys), 4; L-arginyl-L-lysyl-L-arginine (Arg-Lys-Arg), 7; L-lysyl-L-arginyl-L-lysine (Lys-Arg-Lys), 7; L-lysyl-L-arginine (Lys-Arg), 2; out of 12 ORNs, four OE slices; L-arginyl-glycine (Arg-Gly), 10; glycyl-L-arginine (Gly-Arg), 4; L-methionyl-glycine (Met-Gly), 4; glycyl-glycine (Gly-Gly), 4; glycyl-glycyl-glycine (Gly-Gly-Gly), 2; out of six ORNs, four OE slices). (B) Of the five group II peptides only the dipeptide L-arginyl-glycine (Arg-Gly) featured a stimulus-induced maximum amplitude of [Ca2+]i increases comparable to stimulation with L-arginine (only ORNs exclusively sensitive to the amino acid L-arginine, i.e. #27â#30 taken into account). In contrast, the dipeptide glycyl-L-arginine (Gly-Arg) showed a weak response (averaging of multiple applications of glycyl-L-arginine (Gly-Arg); *, p<0.05; **, p<0.001, paired t-test, error bars represent standard deviation). [AA: amino acids, Arg: L-arginine]. | |
Figure 4. Group I and group II peptides elicit significantly different [Ca2+]i transients in individual olfactory receptor neurons.(A) The mean time points of amino acid- and peptide-evoked calcium transient maxima varied for individual stimuli. Transients evoked by group I peptides show a tendency to reach their maximum amplitude later if compared to amino acid stimulations (green, group I peptides, 1 mM; number of responses averaged: AA mix, 67; L-arginine (Arg), 10; L-methionine (Met), 11; L-lysine (Lys), 6; L-arginyl-L-methionine (Arg-Met), 3; L-arginyl-L-methionyl-L-arginine (Arg-Met-Arg), 4; L-methionyl-L-arginyl-L-methionine (Met-Arg-Met), 9; L-methionyl-L-arginine (Met-Arg), 9; L-arginyl-L-lysine (Arg-Lys), 4; L-arginyl-L-lysyl-L-arginine (Arg-Lys-Arg), 7; L-lysyl-L-arginyl-L-lysine (Lys-Arg-Lys), 7; L-lysyl-L-arginine (Lys-Arg), 2; out of 12 ORNs, four OE slices; orange, group II peptides, 200 µM; number of responses averaged: L-arginine (Arg), 7; L-methionine (Met), 3; glycine (Gly), 3; L-arginyl-glycine (Arg-Gly), 10; glycyl-L-arginine (Gly-Arg), 4; L-methionyl-glycine (Met-Gly), 4; glycyl-glycine (Gly-Gly), 4; glycyl-glycyl-glycine (Gly-Gly-Gly), 2; out of six ORNs, four OE slices). (B) A combined analysis reveals that calcium transients evoked by applications of group I peptides show a significant delay of their maximum amplitude if compared to responses to the mixture of amino acids. In contrast, response maxima evoked by group II petides are not significantly shifted in comparison to amino acid controls. Even more clearly, response maxima evoked by L-arginyl-glycine (Arg-Gly) are not shifted if compared to maxima evoked by L-arginine in L-arginine-specific ORNs (not responsive to the other two amino acids L-methionine and glycine). Bars indicate standard deviation and error bars represent the standard error of the mean (*, p<0.0001; unpaired t-test, number of evaluated responses for the first group, AA mix: 67 responses, Pep I: 45 responses, 12 cells, four OE slices; for the second group, AA: 12 responses, Pep II: 25 responses, six cells, four OE slices; and for exclusively L-Arginine positive ORNs, Arg: four responses, Arg-Gly: six responses). (C) Typical responses upon application of amino acids and group I peptides. The maximum amplitude of [Ca2+]i transients induced by group I peptides is smaller and shows a significant delay in comparison to [Ca2+]i transients induced by amino acids. Circles and dotted lines indicate the maximum amplitude of each response. AA mix (200 µM, blue), L-arginyl-L-lysine (Arg-Lys; 1 mM, dark green), L-methionyl-L-arginyl-L-methionine (Met-Arg-Met; 1 mM, green), L-methionyl-L-arginine (Met-Arg; 1 mM, light-green). The odorant application is marked by a grey bar. (D) Representative example of [Ca2+]i transients of an ORN sensitive to L-arginine (200 µM, blue), L-arginyl-glycine (Arg-Gly; 200 µM, orange) and glycyl-L-arginine (Gly-Arg; 200 µM, light-orange). Calcium signals evoked by L-arginyl-glycine showed the highest mean maximum amplitude of all tested peptides. In both peptide responses, the maximum amplitude is not shifted in comparison to the arginine application. [AA mix: amino acid mixture, AA: amino acids, Arg: L-arginine, Met: L-methionine, Lys: L-lysine, Gly: glycine, Pep I: group I peptides, Pep II: group II peptides]. | |
Figure 1. Amino acid- and peptide-induced changes in calcium-dependent fluorescence of individual ORNs in slices of the olfactory epithelium.(A) Slice preparation of the OE of larval Xenopus laevis stained with Fluo-4 AM. The colored ovals (#1â#8) indicate the eight ORNs that were responsive to the mixture of amino acids. (B) Time courses of [Ca2+]i transients of the eight ORNs marked in A, elicited by application of amino acids (L-arginine, L-methionine and L-lysine as a mixture or singularly; each at a concentration of 200 µM) and peptides (consisting of L-arginine, L-methionine and L-lysine; 200 µM and 1 mM). Discernible peptide induced [Ca2+]i transients are marked by an asterisk. To check for ORN viability, the mixture of amino acids was applied at the end of the experiment. (C) Examples of peptide induced calcium transients originating from different ORNs (group I peptides, green, L-arginyl-L-methionine (Arg-Met), 5 mM; L-arginyl-L-methionyl-L-arginine (Arg-Met-Arg), 1 mM; L-methionyl-L-arginyl-L-methionine (Met-Arg-Met), 1 mM; L-methionyl-L-arginine (Met-Arg), 5 mM; L-arginyl-L-lysine (Arg-Lys), 200 µM; L-lysyl-L-arginine (Lys-Arg), 1 mM; L-arginyl-L-lysyl-L-arginine (Arg-Lys-Arg), 1 mM; L-lysyl-L-arginyl-L-lysine (Lys-Arg-Lys), 1 mM;; group II peptides (see Material and Methods), orange, all applied at 200 µM). As reference also the highest amino acid-induced (200 µM) calcium transient is depicted. [AA mix: amino acid mixture]. |
References [+] :
Bischofberger,
Glutamate and N-acetylaspartylglutamate block HVA calcium currents in frog olfactory bulb interneurons via an mGluR2/3-like receptor.
1996, Pubmed,
Xenbase
Bischofberger, Glutamate and N-acetylaspartylglutamate block HVA calcium currents in frog olfactory bulb interneurons via an mGluR2/3-like receptor. 1996, Pubmed , Xenbase
Braubach, Olfactory conditioning in the zebrafish (Danio rerio). 2009, Pubmed
Breunig, The endocannabinoid 2-arachidonoyl-glycerol controls odor sensitivity in larvae of Xenopus laevis. 2010, Pubmed , Xenbase
Caprio, Electrophysiological evidence for acidic, basic, and neutral amino acid olfactory receptor sites in the catfish. 1984, Pubmed
Carr, Chemically stimulated feeding behavior in marine animals : Importance of chemical mixtures and involvement of mixture interactions. 1986, Pubmed
Chiamolera, Minireview: Thyrotropin-releasing hormone and the thyroid hormone feedback mechanism. 2009, Pubmed
Delay, Two second messengers mediate amino acid responses in olfactory sensory neurons of the salamander, Necturus maculosus. 2002, Pubmed
Doolin, Cyclic nucleotide signaling mediates an odorant-suppressible chloride conductance in lobster olfactory receptor neurons. 2005, Pubmed
Doolin, Specificity of odorant-evoked inhibition in lobster olfactory receptor neurons. 2005, Pubmed
Duchamp-Viret, Olfactory discrimination over a wide concentration range. Comparison of receptor cell and bulb neuron abilities. 1990, Pubmed
Duchamp-Viret, Amplifying role of convergence in olfactory system a comparative study of receptor cell and second-order neuron sensitivities. 1989, Pubmed
Friedrich, Chemotopic, combinatorial, and noncombinatorial odorant representations in the olfactory bulb revealed using a voltage-sensitive axon tracer. 1998, Pubmed
Friedrich, Combinatorial and chemotopic odorant coding in the zebrafish olfactory bulb visualized by optical imaging. 1997, Pubmed
Gerlach, Kin recognition in zebrafish: a 24-hour window for olfactory imprinting. 2008, Pubmed
Hansen, Correlation between olfactory receptor cell type and function in the channel catfish. 2003, Pubmed
Hara, Structure-activity relationships of amino acids in fish olfaction. 1976, Pubmed
Hassenklöver, Nucleotide-induced Ca2+ signaling in sustentacular supporting cells of the olfactory epithelium. 2008, Pubmed , Xenbase
Hubbard, Olfactory sensitivity to amino acids in the blackspot sea bream (Pagellus bogaraveo): a comparison between olfactory receptor recording techniques in seawater. 2011, Pubmed
Janecka, Opioid receptors and their ligands. 2004, Pubmed
Junek, Activity correlation imaging: visualizing function and structure of neuronal populations. 2009, Pubmed , Xenbase
Kang, In vivo responses of single olfactory receptor neurons in the channel catfish, Ictalurus punctatus. 1995, Pubmed
Kang, Electro-olfactogram and multiunit olfactory receptor responses to complex mixtures of amino acids in the channel catfish, Ictalurus punctatus. 1991, Pubmed
Kato, Mammalian olfactory receptors: pharmacology, G protein coupling and desensitization. 2009, Pubmed
Kaupp, Olfactory signalling in vertebrates and insects: differences and commonalities. 2010, Pubmed
Krautwurst, Identification of ligands for olfactory receptors by functional expression of a receptor library. 1998, Pubmed
Malnic, Combinatorial receptor codes for odors. 1999, Pubmed
Manzini, Odorant responses of Xenopus laevis tadpole olfactory neurons: a comparison between preparations. 2002, Pubmed , Xenbase
Manzini, Improved fluorescent (calcium indicator) dye uptake in brain slices by blocking multidrug resistance transporters. 2008, Pubmed , Xenbase
Manzini, Classes and narrowing selectivity of olfactory receptor neurons of Xenopus laevis tadpoles. 2004, Pubmed , Xenbase
Manzini, cAMP-independent responses of olfactory neurons in Xenopus laevis tadpoles and their projection onto olfactory bulb neurons. 2002, Pubmed , Xenbase
Manzini, Multidrug resistance transporters in the olfactory receptor neurons of Xenopus laevis tadpoles. 2003, Pubmed , Xenbase
Mezler, Characteristic features and ligand specificity of the two olfactory receptor classes from Xenopus laevis. 2001, Pubmed , Xenbase
Michel, Evidence of a novel transduction pathway mediating detection of polyamines by the zebrafish olfactory system. 2003, Pubmed
Milinski, Mate choice decisions of stickleback females predictably modified by MHC peptide ligands. 2005, Pubmed
Mobley, Odorant responsiveness of squid olfactory receptor neurons. 2008, Pubmed
Mousley, Terminal nerve-derived neuropeptide y modulates physiological responses in the olfactory epithelium of hungry axolotls (Ambystoma mexicanum). 2006, Pubmed
Neale, N-Acetylaspartylglutamate: the most abundant peptide neurotransmitter in the mammalian central nervous system. 2000, Pubmed
Neale, Advances in understanding the peptide neurotransmitter NAAG and appearance of a new member of the NAAG neuropeptide family. 2011, Pubmed
Nikonov, Highly specific olfactory receptor neurons for types of amino acids in the channel catfish. 2007, Pubmed
Rolen, Polyamines as olfactory stimuli in the goldfish Carassius auratus. 2003, Pubmed
Sato, Whole-cell response characteristics of ciliated and microvillous olfactory receptor neurons to amino acids, pheromone candidates and urine in rainbow trout. 2001, Pubmed
Schmachtenberg, Olfactory transduction in ciliated receptor neurons of the Cabinza grunt, Isacia conceptionis (Teleostei: Haemulidae). 2004, Pubmed
Shoji, Amino acids dissolved in stream water as possible home stream odorants for masu salmon. 2000, Pubmed
Speca, Functional identification of a goldfish odorant receptor. 1999, Pubmed , Xenbase
Valentincic, The behavioral detection of binary mixtures of amino acids and their individual components by catfish. 2000, Pubmed
Valentincic, Visual and chemical release of feeding behavior in adult rainbow trout. 1997, Pubmed
Zarzo, The sense of smell: molecular basis of odorant recognition. 2007, Pubmed