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We are analyzing https://link.springer.com/article/10.1186/1471-2202-9-90.

Title:
A large population of diverse neurons in the Drosophilacentral nervous system expresses short neuropeptide F, suggesting multiple distributed peptide functions | BMC Neuroscience
Description:
Background Insect neuropeptides are distributed in stereotypic sets of neurons that commonly constitute a small fraction of the total number of neurons. However, some neuropeptide genes are expressed in larger numbers of neurons of diverse types suggesting that they are involved in a greater diversity of functions. One of these widely expressed genes, snpf, encodes the precursor of short neuropeptide F (sNPF). To unravel possible functional diversity we have mapped the distribution of transcript of the snpf gene and its peptide products in the central nervous system (CNS) of Drosophila in relation to other neuronal markers. Results There are several hundreds of neurons in the larval CNS and several thousands in the adult Drosophila brain expressing snpf transcript and sNPF peptide. Most of these neurons are intrinsic interneurons of the mushroom bodies. Additionally, sNPF is expressed in numerous small interneurons of the CNS, olfactory receptor neurons (ORNs) of the antennae, and in a small set of possibly neurosecretory cells innervating the corpora cardiaca and aorta. A sNPF-Gal4 line confirms most of the expression pattern. None of the sNPF immunoreactive neurons co-express a marker for the transcription factor DIMMED, suggesting that the majority are not neurosecretory cells or large interneurons involved in episodic bulk transmission. Instead a portion of the sNPF producing neurons co-express markers for classical neurotransmitters such as acetylcholine, GABA and glutamate, suggesting that sNPF is a co-transmitter or local neuromodulator in ORNs and many interneurons. Interestingly, sNPF is coexpressed both with presumed excitatory and inhibitory neurotransmitters. A few sNPF expressing neurons in the brain colocalize the peptide corazonin and a pair of dorsal neurons in the first abdominal neuromere coexpresses sNPF and insulin-like peptide 7 (ILP7). Conclusion It is likely that sNPF has multiple functions as neurohormone as well as local neuromodulator/co-transmitter in various CNS circuits, including olfactory circuits both at the level of the first synapse and at the mushroom body output level. Some of the sNPF immunoreactive axons terminate in close proximity to neurosecretory cells producing ILPs and adipokinetic hormone, indicating that sNPF also might regulate hormone production or release.
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Keywords {🔍}

neurons, snpf, cell, bodies, fig, brain, drosophila, cells, pubmed, google, scholar, expression, cas, body, larval, expressing, mushroom, snpfp, small, antiserum, processes, peptide, markers, peptides, gfp, neuropeptide, neurosecretory, cns, immunolabeling, shown, axons, neuronal, dorsal, adult, ventral, snpfgal, neuropeptides, central, abdominal, figure, colocalization, labeling, protocerebrum, situ, interneurons, ganglion, snpfpir, detected, lobe, subesophageal,

Topics {✒️}

nitroblue tetrazolium/5-bromo-4-chloro-3-indolyl phosphate met-enkephalin-arg6-gly7-leu8 recrystallized α-cyano-4-hydroxycinnamic acid e2 c929-gal4-driven gfp met-enkephalin-arg6-phe7 coexpressed cha-gal4-driven gfp direct maldi-tof profiling threshold-based surface generation maldi-tof mass spectra stereotyped odor-evoked activity snpfp-ir fibers invading texture-based volume rendering maldi-tof-tof fragmentation tyrosine decarboxylase-driven gfp tyrosine-hydroxylase promoter-gal4 extracellular signal-related kinases central nervous system neuropeptide f-promoter-gal4 varicose snpfp-ir processes mai179-gal4 drives gfp choline acetyltransferase-expressing neurons threshold-based 3d reconstruction tyrosine hydroxylase-immunoreactive neurons snpfp-ir cell bodies impinging snpf-ir terminations snpfp-immunolabled axon terminations drosophila nervous system snpf-gal4 line confirms snpf-ir processes impinging snpf-derived precursor protein snpf-expressing terminations impinge adult nervous system snpf-ir cell bodies c929-gal4-driven gfp dorso-median cell body dig-labeled snpf riboprobes references o'shea cha-gal4-driven gfp gad1 -gal4-driven gfp snpfp-ir axon tracts mosquito host-seeking behavior strongly expressing snpf-gal4 article download pdf flies bearing snpf-gal4 snpf-gal4 driven gfp snpf-gal4-driven gfp santos & christian wegener snpf-ir axons terminate cha-gal4 expressing neurons vesicular glutamate transporter-gal4

Questions {❓}

  • Functions of sNPF: diverse or not?
  • How many peptides are produced by the snpfgene?
  • Or, differently phrased, does a given peptide expressed in a diverse set of neuronal circuits and neuron types (including neurosecretory cells) subserve a global unified function or a multitude of separate distributed functions?

Schema {🗺️}

WebPage:
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         description:Insect neuropeptides are distributed in stereotypic sets of neurons that commonly constitute a small fraction of the total number of neurons. However, some neuropeptide genes are expressed in larger numbers of neurons of diverse types suggesting that they are involved in a greater diversity of functions. One of these widely expressed genes, snpf, encodes the precursor of short neuropeptide F (sNPF). To unravel possible functional diversity we have mapped the distribution of transcript of the snpf gene and its peptide products in the central nervous system (CNS) of Drosophila in relation to other neuronal markers. There are several hundreds of neurons in the larval CNS and several thousands in the adult Drosophila brain expressing snpf transcript and sNPF peptide. Most of these neurons are intrinsic interneurons of the mushroom bodies. Additionally, sNPF is expressed in numerous small interneurons of the CNS, olfactory receptor neurons (ORNs) of the antennae, and in a small set of possibly neurosecretory cells innervating the corpora cardiaca and aorta. A sNPF-Gal4 line confirms most of the expression pattern. None of the sNPF immunoreactive neurons co-express a marker for the transcription factor DIMMED, suggesting that the majority are not neurosecretory cells or large interneurons involved in episodic bulk transmission. Instead a portion of the sNPF producing neurons co-express markers for classical neurotransmitters such as acetylcholine, GABA and glutamate, suggesting that sNPF is a co-transmitter or local neuromodulator in ORNs and many interneurons. Interestingly, sNPF is coexpressed both with presumed excitatory and inhibitory neurotransmitters. A few sNPF expressing neurons in the brain colocalize the peptide corazonin and a pair of dorsal neurons in the first abdominal neuromere coexpresses sNPF and insulin-like peptide 7 (ILP7). It is likely that sNPF has multiple functions as neurohormone as well as local neuromodulator/co-transmitter in various CNS circuits, including olfactory circuits both at the level of the first synapse and at the mushroom body output level. Some of the sNPF immunoreactive axons terminate in close proximity to neurosecretory cells producing ILPs and adipokinetic hormone, indicating that sNPF also might regulate hormone production or release.
         datePublished:2008-09-19T00:00:00Z
         dateModified:2008-09-19T00:00:00Z
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            Mushroom Body
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      headline:A large population of diverse neurons in the Drosophilacentral nervous system expresses short neuropeptide F, suggesting multiple distributed peptide functions
      description:Insect neuropeptides are distributed in stereotypic sets of neurons that commonly constitute a small fraction of the total number of neurons. However, some neuropeptide genes are expressed in larger numbers of neurons of diverse types suggesting that they are involved in a greater diversity of functions. One of these widely expressed genes, snpf, encodes the precursor of short neuropeptide F (sNPF). To unravel possible functional diversity we have mapped the distribution of transcript of the snpf gene and its peptide products in the central nervous system (CNS) of Drosophila in relation to other neuronal markers. There are several hundreds of neurons in the larval CNS and several thousands in the adult Drosophila brain expressing snpf transcript and sNPF peptide. Most of these neurons are intrinsic interneurons of the mushroom bodies. Additionally, sNPF is expressed in numerous small interneurons of the CNS, olfactory receptor neurons (ORNs) of the antennae, and in a small set of possibly neurosecretory cells innervating the corpora cardiaca and aorta. A sNPF-Gal4 line confirms most of the expression pattern. None of the sNPF immunoreactive neurons co-express a marker for the transcription factor DIMMED, suggesting that the majority are not neurosecretory cells or large interneurons involved in episodic bulk transmission. Instead a portion of the sNPF producing neurons co-express markers for classical neurotransmitters such as acetylcholine, GABA and glutamate, suggesting that sNPF is a co-transmitter or local neuromodulator in ORNs and many interneurons. Interestingly, sNPF is coexpressed both with presumed excitatory and inhibitory neurotransmitters. A few sNPF expressing neurons in the brain colocalize the peptide corazonin and a pair of dorsal neurons in the first abdominal neuromere coexpresses sNPF and insulin-like peptide 7 (ILP7). It is likely that sNPF has multiple functions as neurohormone as well as local neuromodulator/co-transmitter in various CNS circuits, including olfactory circuits both at the level of the first synapse and at the mushroom body output level. Some of the sNPF immunoreactive axons terminate in close proximity to neurosecretory cells producing ILPs and adipokinetic hormone, indicating that sNPF also might regulate hormone production or release.
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      dateModified:2008-09-19T00:00:00Z
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         Green Fluorescent Protein
         Mushroom Body
         Antennal Lobe
         Optic Lobe
         Ventral Nerve Cord
         Neurosciences
         Neurobiology
         Animal Models
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            name:Christian Wegener
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                  address:
                     name:Emmy Noether Neuropeptide Group, Department of Biology, Animal Physiology, Philipps-University, Marburg, Germany
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                  name:Stockholm University
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               type:PostalAddress
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      name:Jonathan G Santos
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            name:Philipps-University
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               name:Emmy Noether Neuropeptide Group, Department of Biology, Animal Physiology, Philipps-University, Marburg, Germany
               type:PostalAddress
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            address:
               name:Department of Zoology, Stockholm University, Stockholm, Sweden
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      name:Emmy Noether Neuropeptide Group, Department of Biology, Animal Physiology, Philipps-University, Marburg, Germany
      name:Department of Zoology, Stockholm University, Stockholm, Sweden

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