The DOI matches its Crossref record; 92 of the 92 references it cites were found in a registry or an index.
Multiple neuropeptides in the Drosophila antennal lobe suggest complex modulatory circuits
Abstract
The fruitfly, Drosophila, is dependent on its olfactory sense in food search and reproduction. Processing of odorant information takes place in the antennal lobes, the primary olfactory center in the insect brain. Besides classical neurotransmitters, earlier studies have indicated the presence of a few neuropeptides in the olfactory system. In the present study we made an extensive analysis of the expression of neuropeptides in the Drosophila antennal lobes by direct profiling using matrix‐assisted laser desorption/ionization‐time‐of‐flight (MALDI‐TOF) mass spectrometry and immunocytochemistry. Neuropeptides from seven different precursor genes were unambiguously identified and their localization in neurons was subsequently revealed by immunocytochemistry. These were short neuropeptide F, tachykinin related peptide, allatostatin A, myoinhibitory peptide, SIFamide, IPNamide, and myosuppressin. The neuropeptides were expressed in subsets of olfactory sensory cells and different populations of local interneurons and extrinsic (centrifugal) neurons. In some neuron types neuropeptides were colocalized with classical neurotransmitters. Our findings suggest a huge complexity in peptidergic signaling in different circuits of the antennal lobe. J. Comp. Neurol. 518:3359–3380, 2010. © 2010 Wiley‐Liss, Inc.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“They seem to break Dale’s law104,106 and Lacin’s law (Figure 7C), with similar morphology types predicted to express different transmitters (Figures S5F and S5G).”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
In the citing paper
“The fan-shaped body is known to express leucokinin, allatostatin A, short neuropeptide F, Drosophila neuropeptide F, tachykinin, proctolin, dFMRFa, SIFamide and myoinhibitory peptide in a highly specific and layer-wise manner.106,175,177,184”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
In the citing paper
“transmitter usage in these local neurons seems to break Dale’s law,104,106 Lacin’s law (Figure 7C) and the expectation of uniform transmitter expression within a type (Figures S5F and S5G)”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
In the citing paper
“We suspect that some cholinergic local neurons have been mispredicted dopaminergic because at least ∼ 3 cholinergic neurons co-express allatostatin A and ∼ 10-15 co-express myoinhibitory peptide.106”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
In the citing paper
“Tachykinin is also known to co-express in ∼ 40 GABAergic ‘ALl1 dorsal’ neurons per hemisphere106”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
Citations
Cites
Coding of Odors by a Receptor Repertoire
Hallem, E. A., & Carlson, J. R. (2006) · Cell · doi:10.1016/j.cell.2006.01.050 · Cited by 1,286
An Olfactory Sensory Map in the Fly Brain
Vosshall, L. B., Wong, A. M., & Axel, R. (2000) · Cell · doi:10.1016/s0092-8674(00)00021-0 · Cited by 1,090
Molecular, Anatomical, and Functional Organization of the Drosophila Olfactory System
Couto, A., Alenius, M., & Dickson, B. J. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.034 · Cited by 967
The organization of the chemosensory system in Drosophila melanogaster: a rewiew
Stocker, R. F. (1994) · Cell and Tissue Research · doi:10.1007/bf00305372 · Cited by 950
Bruchpilot Promotes Active Zone Assembly, Ca 2+ Channel Clustering, and Vesicle Release
Kittel, R. J., Wichmann, C., Rasse, T. M., Fouquet, W., Schmidt, M., Schmid, A., Wagh, D. A., Pawlu, C., Kellner, R. R., Willig, K. I., et al. (2006) · Science · doi:10.1126/science.1126308 · Cited by 772
A single class of olfactory neurons mediates behavioural responses to a Drosophila sex pheromone
Kurtović-Kozarić, A., Widmer, A., & Dickson, B. J. (2007) · Nature · doi:10.1038/nature05672 · Cited by 761
Genetic and Functional Subdivision of the Drosophila Antennal Lobe
Fishilevich, E., & Vosshall, L. B. (2005) · Current Biology · doi:10.1016/j.cub.2005.07.066 · Cited by 608
Olfactory Perception: Receptors, Cells, and Circuits
Su, C., Menuz, K., & Carlson, J. R. (2009) · Cell · doi:10.1016/j.cell.2009.09.015 · Cited by 599
Invertebrate Synapsins: A Single Gene Codes for Several Isoforms inDrosophila
Klagges, B. R. E., Heimbeck, G., Godenschwege, T. A., Hofbauer, A., Pflugfelder, G. O., Reifegerste, R., Reisch, D., Schaupp, M., Buchner, S., & Buchner, E. (1996) · Journal of Neuroscience · doi:10.1523/jneurosci.16-10-03154.1996 · Cited by 489
Wilson, R. I., & Laurent, G. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2070-05.2005 · Cited by 484
Flagged first, then by citations
Cited by
Sorted by citations
A Single-Cell Transcriptome Atlas of the Aging Drosophila Brain
Davie, K., Janssens, J., Koldere, D., De Waegeneer, M., Pech, U., Kreft, Ł., Aibar, S., Makhzami, S., Christiaens, V., Bravo González-Blas, C., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.057 · Cited by 840
Presynaptic facilitation by neuropeptide signaling mediates odor-driven food search
Root, C. M., Ko, K. I., Jafari, A., & Wang, J. W. (2011) · Cell · doi:10.1016/j.cell.2011.02.008 · Cited by 526
Early Olfactory Processing in Drosophila: Mechanisms and Principles
Wilson, R. I. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150533 · Cited by 394
Recent advances in neuropeptide signaling in Drosophila, from genes to physiology and behavior
Nässel, D. R., & Zandawala, M. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.02.003 · Cited by 373
Self-citationNässel, D. R., & Wegener, C. (2011) · Peptides · doi:10.1016/j.peptides.2011.03.013 · Cited by 324
Self-citationEckstein, N., Bates, A. S., Champion, A., Du, M., Yin, Y., Schlegel, P., Lu, A. K.-Y., Rymer, T., Finley-May, S., Paterson, T., et al. (2024) · Cell · doi:10.1016/j.cell.2024.03.016 · Cited by 277
Elucidating the Neuronal Architecture of Olfactory Glomeruli in the Drosophila Antennal Lobe
Grabe, V., Baschwitz, A., Dweck, H. K. M., Lavista-Llanos, S., Hansson, B. S., & Sachse, S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.063 · Cited by 186
Metabolism and growth adaptation to environmental conditions in Drosophila
Koyama, T., Texada, M. J., Halberg, K. A., & Rewitz, K. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03547-2 · Cited by 152
Olfactory coding in the insect brain: data and conjectures
Galizia, C. G. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12558 · Cited by 163
Tachykinins: Neuropeptides That Are Ancient, Diverse, Widespread and Functionally Pleiotropic
Nässel, D. R., Zandawala, M., Kawada, T., & Satake, H. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01262 · Cited by 153
Self-citationNässel, D. R. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00083 · Cited by 119
Self-citationMyoinhibitory peptide regulates feeding in the marine annelid Platynereis
Williams, E. A., Conzelmann, M., & Jékely, G. (2015) · Frontiers in Zoology · doi:10.1186/s12983-014-0093-6 · Cited by 120
Cannell, E., Dornan, A. J., Halberg, K. A., Terhzaz, S., Dow, J. A. T., & Davies, S. A. (2016) · Peptides · doi:10.1016/j.peptides.2016.02.004 · Cited by 119
Synaptic organization of the Drosophila antennal lobe and its regulation by the Teneurins
Mosca, T. J., & Luo, L. (2014) · eLife · doi:10.7554/elife.03726 · Cited by 117
Kahsai, L., & Winther, Å. M. E. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22520 · Cited by 115
Neuropeptides Modulate Female Chemosensory Processing upon Mating in Drosophila
Hussain, A., Üçpunar, H. K., Zhang, M., Loschek, L. F., & Kadow, I. C. G. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002455 · Cited by 113
Neuropeptide modulation of microcircuits
Nusbaum, M. P., & Blitz, D. M. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.01.003 · Cited by 107
The CCHamide 1 receptor modulates sensory perception and olfactory behavior in starved Drosophila
Farhan, A., Gulati, J., Große‐Wilde, E., Vogel, H., Hansson, B. S., & Knaden, M. (2013) · Scientific Reports · doi:10.1038/srep02765 · Cited by 92
Regulation of insect behavior via the insulin-signaling pathway
Erion, R., & Sehgal, A. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00353 · Cited by 92
Endocrine cybernetics: neuropeptides as molecular switches in behavioural decisions
Nässel, D. R., & Zandawala, M. (2022) · Open Biology · doi:10.1098/rsob.220174 · Cited by 85
Self-citationFeeding regulates sex pheromone attraction and courtship in Drosophila females
Lebreton, S., Trona, F., Borrero‐Echeverry, F., Bilz, F., Grabe, V., Becher, P. G., Carlsson, M. A., Nässel, D. R., Hansson, B. S., Sachse, S., et al. (2015) · Scientific Reports · doi:10.1038/srep13132 · Cited by 83
Self-citationChrist, P., Reifenrath, A., Kahnt, J., Hauser, F., Hill, S. R., Schachtner, J., & Ignell, R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188243 · Cited by 79
Self-citationFood odors trigger an endocrine response that affects food ingestion and metabolism
Lushchak, O. V., Carlsson, M. A., & Nässel, D. R. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1884-4 · Cited by 67
Self-citationMusashe, D. T., Purice, M. D., Speese, S. D., Doherty, J., & Logan, M. A. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.022 · Cited by 58
Sayın, S., Boehm, A. C., Kobler, J. M., Backer, J. D., & Kadow, I. C. G. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00011 · Cited by 60
Intrinsic and Extrinsic Neuromodulation of Olfactory Processing
Lizbinski, K. M., & Dacks, A. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00424 · Cited by 60
Neuropeptides in the antennal lobe of the yellow fever mosquito, Aedes aegypti
Siju, K. P., Reifenrath, A., Scheiblich, H., Neupert, S., Predel, R., Hansson, B. S., Schachtner, J., & Ignell, R. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23434 · Cited by 59
Self-citationDrosophila olfaction: past, present and future
Benton, R. (2022) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2022.2054 · Cited by 62
Neuropeptides in insect mushroom bodies
Heuer, C. M., Kollmann, M., Binzer, M., & Schachtner, J. (2012) · Arthropod Structure & Development · doi:10.1016/j.asd.2012.02.005 · Cited by 53
Self-citationNeurogenetics of Female Reproductive Behaviors in Drosophila melanogaster
Laturney, M., & Billeter, J. (2014) · Advances in genetics · doi:10.1016/b978-0-12-800271-1.00001-9 · Cited by 55
Lange, A. B., Alim, U., Vandersmissen, H. P., Mizoguchi, A., Broeck, J. V., & Orchard, I. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00098 · Cited by 50
Nagata, S., Matsumoto, S., Nakane, T., Ohara, A., Morooka, N., Konuma, T., Nagai‐Okatani, C., & Nagasawa, H. (2012) · Frontiers in Endocrinology · doi:10.3389/fendo.2012.00003 · Cited by 48
Neuropeptides in modulation of Drosophila behavior: how to get a grip on their pleiotropic actions
Nässel, D. R., Pauls, D., & Huetteroth, W. (2019) · Current Opinion in Insect Science · doi:10.1016/j.cois.2019.03.002 · Cited by 48
Self-citationModulation of neural circuits: how stimulus context shapes innate behavior in Drosophila
Su, C.-Y., & Wang, J. W. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.04.008 · Cited by 48
Sizemore, T. R., & Dacks, A. M. (2016) · Scientific Reports · doi:10.1038/srep37119 · Cited by 48
Olfactory Habituation in Drosophila—Odor Encoding and its Plasticity in the Antennal Lobe
Isabell, T., Lee, J. A., & Ramaswami, M. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63350-7.00001-2 · Cited by 46
Spit, J., Badisco, L., Verlinden, H., Wielendaele, P. V., Zels, S., Dillen, S., & Broeck, J. V. (2012) · Canadian Journal of Zoology · doi:10.1139/z2012-014 · Cited by 42
Serotonergic modulation across sensory modalities
Sizemore, T. R., Hurley, L. M., & Dacks, A. M. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00034.2020 · Cited by 44
Coates, K. E., Majot, A. T., Zhang, X., Michael, C. T., Spitzer, S. L., Gaudry, Q., & Dacks, A. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0192-17.2017 · Cited by 39
Carlsson, M. A., Enell, L. E., & Nässel, D. R. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1660-4 · Cited by 40
Self-citationBrain organization in Collembola (springtails)
Kollmann, M., Huetteroth, W., & Schachtner, J. (2011) · Arthropod Structure & Development · doi:10.1016/j.asd.2011.02.003 · Cited by 40
Self-citationKidd, S., Struhl, G., & Lieber, T. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005244 · Cited by 42
Levy, C., Brooks, J. M., Chen, J., Su, J., & Fox, M. A. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23701 · Cited by 40
Organization of the Olfactory System of Nymphalidae Butterflies
Carlsson, M. A., Schäpers, A., Nässel, D. R., & Janz, N. (2013) · Chemical Senses · doi:10.1093/chemse/bjt008 · Cited by 37
Self-citationThe Wiring Logic of an Identified Serotonergic Neuron That Spans Sensory Networks
Coates, K. E., Calle-Schuler, S. A., Helmick, L. M., Knotts, V. L., Martik, B. N., Salman, F., Warner, L. T., Valla, S. V., Bock, D. D., & Dacks, A. M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0552-20.2020 · Cited by 38
Peptidomics and processing of regulatory peptides in the fruit fly Drosophila
Pauls, D., Chen, J., Reiher, W., Vanselow, J. T., Schlösser, A., Kahnt, J., & Wegener, C. (2014) · EuPA Open Proteomics · doi:10.1016/j.euprot.2014.02.007 · Cited by 32
Jung, J. W., Kim, J., Pfeiffer, R., Ahn, Y., Page, T. L., & Kwon, H. W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081361 · Cited by 35
Lu, H., & Pietrantonio, P. V. (2011) · BMC Neuroscience · doi:10.1186/1471-2202-12-57 · Cited by 35
Fine structure of synaptic sites and circuits in mushroom bodies of insect brains
Schürmann, F. (2016) · Arthropod Structure & Development · doi:10.1016/j.asd.2016.08.005 · Cited by 37
Structure and function of neuropeptide F in insects
Cui, H., & Zhao, Z. (2020) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(19)62804-2 · Cited by 34
Nässel, D. R. (2012) · Canadian Journal of Zoology · doi:10.1139/z2012-009 · Cited by 41
Self-citationWilson, R. I. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.03.002 · Cited by 32
Presynaptic modulation of early olfactory processing in Drosophila
Wang, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20936 · Cited by 36
Neuroblast lineage-specific origin of the neurons of the Drosophila larval olfactory system
Das, A., Gupta, T., Davla, S., Prieto-Godino, L. L., Diegelmann, S., Reddy, O. V., Raghavan, K. V., Reichert, H., Lovick, J. K., & Hartenstein, V. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.11.003 · Cited by 30
Neuropeptidomics of the Carpenter Ant Camponotus floridanus
Schmitt, F., Vanselow, J. T., Schlösser, A., Kahnt, J., Rößler, W., & Wegener, C. (2015) · Journal of Proteome Research · doi:10.1021/pr5011636 · Cited by 32
Neuropeptidome of Tribolium castaneum antennal lobes and mushroom bodies
Binzer, M., Heuer, C. M., Kollmann, M., Kahnt, J., Hauser, F., Grimmelikhuijzen, C. J. P., & Schachtner, J. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23399 · Cited by 31
Self-citationHigh-resolution AP-SMALDI mass spectrometry imaging of Drosophila melanogaster
Khalil, S. M., Pretzel, J., Becker, K., & Spengler, B. (2017) · International Journal of Mass Spectrometry · doi:10.1016/j.ijms.2017.04.001 · Cited by 31
Lehmann, P., Nylin, S., Gotthard, K., & Carlsson, M. A. (2017) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2017.0897 · Cited by 30
Self-citationNutrient Sensing via Gut in Drosophila melanogaster
Chopra, G., Kaushik, S., & Kain, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052694 · Cited by 40
Schulze, J., Neupert, S., Schmidt, L., Predel, R., Lamkemeyer, T., Homberg, U., & Stengl, M. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22785 · Cited by 30
Singh, A. P., Das, R. N., Kidiyoor, G. R., Aggarwal, A., Diegelmann, S., Evers, J. F., Karandikar, H., Landgraf, M., Rodrigues, V., & VijayRaghavan, K. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003452 · Cited by 30
Calcium Imaging of Neural Activity in the Olfactory System of Drosophila
Strutz, A., Völler, T., Riemensperger, T. D., Fiala, A., & Sachse, S. (2012) · Neuromethods · doi:10.1007/978-1-62703-014-4_3 · Cited by 28
Distributed control circuits across a brain-and-cord connectome
Bates, A. S., Phelps, J. S., Kim, M., Yang, H. H., Matsliah, A., Ajabi, Z., Perlman, E., Delgado, K. M., Osman, M. A. M., Salmon, C. K., et al. (2026) · Nature · doi:10.1038/s41586-026-10735-w · Cited by 76
Jung, J., Kim, D., Han, G.-Y., & Kwon, H. W. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102855 · Cited by 29
Kołodziejczyk, A. M., & Nässel, D. R. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1100-7 · Cited by 27
Self-citationFuscà, D., Schachtner, J., & Kloppenburg, P. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23757 · Cited by 24
Self-citationShort Neuropeptide F and Its Receptor Regulate Feeding Behavior in Pea Aphid (Acyrthosiphon pisum)
Amir, M. B., Shi, Y., Cao, H., Ali, M. Y., Ahmed, M. A., Smagghe, G. J., & Liu, T. (2022) · Insects · doi:10.3390/insects13030282 · Cited by 25
Kidd, S., & Lieber, T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151279 · Cited by 25
Sex peptides and MIPs can activate the same G protein-coupled receptor
Vandersmissen, H. P., Nachman, R. J., & Broeck, J. V. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.02.014 · Cited by 24
Structural plasticity of olfactory neuropils in relation to insect diapause
Eriksson, M., Janz, N., Nylin, S., & Carlsson, M. A. (2020) · Ecology and Evolution · doi:10.1002/ece3.7046 · Cited by 23
Self-citationVariations on a Theme: Antennal Lobe Architecture across Coleoptera
Kollmann, M., Schmidt, R., Heuer, C. M., & Schachtner, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166253 · Cited by 23
Self-citationFunctional characterization of mosquito short neuropeptide F receptors
Christ, P., Hill, S. R., Schachtner, J., Hauser, F., & Ignell, R. (2018) · Peptides · doi:10.1016/j.peptides.2018.03.009 · Cited by 20
Self-citationOdor processing in the cockroach antennal lobe—the network components
Fuscà, D., & Kloppenburg, P. (2021) · Cell and Tissue Research · doi:10.1007/s00441-020-03387-3 · Cited by 21
The ability of Drosophila hybrids to locate food declines with parental divergence
Turissini, D. A., Comeault, A. A., Geoffrey, L., Lee, Y. C. G., & Matute, D. R. (2017) · Evolution · doi:10.1111/evo.13180 · Cited by 21
Gellerer, A., Franke, A., Neupert, S., Predel, R., Zhou, X. Y., Liu, S., Reiher, W., Wegener, C., & Homberg, U. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23671 · Cited by 21
Li, Y., Hoxha, V., Lama, C., Dinh, B. H., Vo, C. N., & Dauwalder, B. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028269 · Cited by 18
Bendena, W. G., Campbell, J. C., Zara, L. C., Tobe, S. S., & Chin-Sang, I. D. (2012) · Frontiers in Endocrinology · doi:10.3389/fendo.2012.00093 · Cited by 19
Sizemore, T. R., Jonaitis, J., & Dacks, A. M. (2023) · Nature Communications · doi:10.1038/s41467-023-41012-3 · Cited by 21
Schmitt, F., Vanselow, J. T., Schlösser, A., Wegener, C., & Rößler, W. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24109 · Cited by 18
Fruit fly behavior in response to chemosensory signals
Herrero, P. (2012) · Peptides · doi:10.1016/j.peptides.2012.09.019 · Cited by 18
Dacks, A. M., & Nighorn, A. J. (2010) · Chemical Senses · doi:10.1093/chemse/bjq121 · Cited by 17
The neuropeptide SIFamide in the brain of three cockroach species
Arendt, A., Neupert, S., Schendzielorz, J., Predel, R., & Stengl, M. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23910 · Cited by 17
Lebreton, S., Carlsson, M. A., & Witzgall, P. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00685 · Cited by 15
Self-citationLiu, Y., Luo, J., & Nässel, D. R. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00097 · Cited by 14
Self-citationNovel antennal lobe substructures revealed in the small hive beetle Aethina tumida
Kollmann, M., Rupenthal, A. L., Neumann, P., Huetteroth, W., & Schachtner, J. (2015) · Cell and Tissue Research · doi:10.1007/s00441-015-2282-9 · Cited by 14
Self-citationInsect brain plasticity: effects of olfactory input on neuropil size
Eriksson, M., Nylin, S., & Carlsson, M. A. (2019) · Royal Society Open Science · doi:10.1098/rsos.190875 · Cited by 14
Self-citationWhat Drosophila can tell us about state-dependent peptidergic signaling in insects
Nässel, D. R. (2025) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2025.104275 · Cited by 13
Self-citationShort neuropeptide F in integrated insect physiology
Cholewiński, M., Chowański, S., Lubawy, J., Urbański, A., Walkowiak‐Nowicka, K., & Marciniak, P. (2024) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2300355 · Cited by 12
The degradome and the evolution of Drosophila sex peptide as a ligand for the MIP receptor
Isaac, R. E., Kim, Y., & Audsley, N. (2014) · Peptides · doi:10.1016/j.peptides.2013.12.016 · Cited by 12
Diesner, M., Gallot, A., Binz, H., Gaertner, C., Vitecek, S., Kahnt, J., Schachtner, J., Jacquin‐Joly, E., & Gadenne, C. (2018) · Journal of Proteome Research · doi:10.1021/acs.jproteome.7b00779 · Cited by 12
Self-citationArguello, J. R., Abuin, L., Armida, J., Mika, K., Chai, P. C., & Benton, R. (2021) · eLife · doi:10.7554/elife.63036 · Cited by 11
Kołodziejczyk, A. M., & Nässel, D. R. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1198-2 · Cited by 12
Self-citationLismont, E., Mortelmans, N., Verlinden, H., & Broeck, J. V. (2017) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.10.014 · Cited by 12
Lizbinski, K. M., Marsat, G., & Dacks, A. M. (2018) · eNeuro · doi:10.1523/eneuro.0212-18.2018 · Cited by 15
Trebels, B., Dippel, S., Goetz, B., Graebner, M., Hofmann, C., Hofmann, F., Schmid, F.-R., Uhl, M., Vuong, M.-P., Weber, V., et al. (2021) · BMC Biology · doi:10.1186/s12915-021-01055-8 · Cited by 11
Self-citationSynaptic connectome of a neurosecretory network in the Drosophila brain
McKim, T. H., Gera, J., Gayban, A. J. B., Christie, K., Shin, J., Reinhard, N., Manoli, G., Hilpert, S., Callaerts, P., van Breugel, F., et al. (2026) · eLife · doi:10.1101/2024.08.28.609616 · Cited by 17
Functional characterization of the dual allatostatin-A receptors in mosquitoes
Christ, P., Hill, S. R., Schachtner, J., Hauser, F., & Ignell, R. (2017) · Peptides · doi:10.1016/j.peptides.2017.10.016 · Cited by 11
Self-citationSalisbury, J. P., Boggio, K. J., Hsu, Y. A., Quijada, J. V., Sivachenko, A., Gloeckner, G., Kowalski, P. J., Easterling, M. L., Rosbash, M., & Agar, J. N. (2013) · Molecular Brain · doi:10.1186/1756-6606-6-60 · Cited by 11
The anatomical basis for modulatory convergence in the antennal lobe of Manduca sexta
Lizbinski, K. M., Metheny, J. D., Bradley, S. P., Kesari, A., & Dacks, A. M. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23926 · Cited by 9
Odor response adaptation in Drosophila—a continuous individualization process
Jafari, S., & Alenius, M. (2021) · Cell and Tissue Research · doi:10.1007/s00441-020-03384-6 · Cited by 10
Metadata
- Authors
- Carlsson, M. A., Diesner, M., Schachtner, J., & Nässel, D. R.
- Affiliations
- Stockholm University (SE)
- Philipps University of Marburg (DE)
- Corresponding author
- Carlsson, Mikael A.
- Nässel, Dick R.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 2010-06-23
- Volume
- 518
- Issue
- 16
- Pages
- 3359-3380
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1979540477
- Cited by
- 146
- References
- 92
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 8 · 2023: 6 · 2022: 5 · 2021: 12 · 2020: 5 · 2019: 4 · 2018: 9 · 2017: 11 · 2016: 10 · 2015: 11 · 2014: 13 · 2013: 12 · 2012: 13
- FWCI
- 5.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- neuropeptides, olfactory system, short neuropeptide F, tachykinin-related peptides, allatostatin A, myoinhibitory peptides, SIFamide, myosuppressin, olfactory sensory neurons, local interneurons, neurotransmitter co-localization, peptidergic signaling, olfactory processing
- MeSH terms
- Amino Acid Sequence, Animals, Brain, Drosophila melanogaster, Female, Hormone Antagonists, Interneurons, Male, Molecular Sequence Data, Neuropeptides, Olfactory Pathways, Smell, Signal Transduction, Olfactory Receptor Neurons, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Drosophila Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review