References
- Beehler-Evans, R., and Micchelli, C.A. (2015). Generation of enteroendocrine cell diversity in midgut stem cell lineages. Development 142, 654-664. https://doi.org/10.1242/dev.114959
- Brogiolo, W., Stocker, H., Ikeya, T., Rintelen, F., Fernandez, R., and Hafen, E. (2001). An evolutionarily conserved function of the Drosophila insulin receptor and insulin-like peptides in growth control. Curr. Biol. 11, 213-221. https://doi.org/10.1016/S0960-9822(01)00068-9
- Brown, M.R., Crim, J.W., Arata, R.C., Cai, H.N., Chun, C., and Shen, P. (1999). Identification of a Drosophila brain-gut peptide related to the neuropeptide Y family. Peptides 20, 1035-1042. https://doi.org/10.1016/S0196-9781(99)00097-2
- Chen, Y., Veenstra, J.A., Davis, N.T., and Hagedorn, H.H. (1994). comparative study of leucokinin-immunoreactive neurons in insects. Cell Tissue Res. 276, 69-83. https://doi.org/10.1007/BF00354786
- Chen, J., Choi, M.S., Mizoguchi, A., Veenstra, J.A., Kang, K., Kim, Y.J., and Kwon, J.Y. (2015). Isoform-specific expression of the neuropeptide orcokinin in Drosophila melanogaster. Peptides 68, 50-57. https://doi.org/10.1016/j.peptides.2015.01.002
- Dubreuil, R.R. (2004). Copper cells and stomach acid secretion in the Drosophila midgut. Int. J. Biochem. Cell Biol. 36, 745-752.
- Engelstoft, M.S., Egerod, K.L., Lund, M.L., and Schwartz, T.W. (2013). Enteroendocrine cell types revisited. Curr. Opin. Pharmacol. 13, 912-921. https://doi.org/10.1016/j.coph.2013.09.018
- Hansen, K.K., Hauser, F., Williamson, M., Weber, S.B., and Grimmelikhuijzen, C.J. (2011). The Drosophila genes CG14593 and CG30106 code for G-protein-coupled receptors specifically activated by the neuropeptides CCHamide-1 and CCHamide-2. Biochem. Biophys. Res. Commun. 404, 184-189. https://doi.org/10.1016/j.bbrc.2010.11.089
- Hergarden, A.C., Tayler, T.D., and Anderson, D.J. (2012). Allatostatin- A neurons inhibit feeding behavior in adult Drosophila. Proc. Natl. Acad. Sc.i USA 109, 3967-3972. https://doi.org/10.1073/pnas.1200778109
- LaJeunesse, D.R., Johnson, B., Presnell, J.S., Catignas, K.K., and Zapotoczny, G. (2010). Peristalsis in the junction region of the Drosophila larval midgut is modulated by DH31 expressing enteroendocrine cells. BMC Physiol. 10, 14. https://doi.org/10.1186/1472-6793-10-14
- Lee, T., and Luo, L. (1999). Mosaic analysis with a repressible cell marker for studies of gene function in neuronal morphogenesis. Neuron 22, 451-461. https://doi.org/10.1016/S0896-6273(00)80701-1
- Lee, G., and Park, J.H. (2004). Hemolymph sugar homeostasis and starvation-induced hyperactivity affected by genetic manipulations of the adipokinetic hormone-encoding gene in Drosophila melanogaster. Genetics 167, 311-323. https://doi.org/10.1534/genetics.167.1.311
- Lee, K.S., You, K.H., Choo, J.K., Han, Y.M., and Yu, K. (2004). Drosophila short neuropeptide F regulates food intake and body size. J. Biol. Chem. 279, 50781-50789. https://doi.org/10.1074/jbc.M407842200
- Lee, K.S., Kwon, O.Y., Lee, J.H., Kwon, K., Min, K.J., Jung, S.A., Kim, A.K., You, K.H., Tatar, M., and Yu, K. (2008). Drosophila short neuropeptide F signalling regulates growth by ERKmediated insulin signalling. Nat. Cell Biol. 10, 468-475. https://doi.org/10.1038/ncb1710
- Li, S., Torre-Muruzabal, T., Sogaard, K.C., Ren, G.R., Hauser, F., Engelsen, S.M., Podenphanth, M.D., Desjardins, A., and Grimmelikhuijzen, C.J. (2013). Expression patterns of the Drosophila neuropeptide CCHamide-2 and its receptor may suggest hormonal signaling from the gut to the brain. PLoS ONE 8, e76131. https://doi.org/10.1371/journal.pone.0076131
- Luan, H., Lemon, W.C., Peabody, N.C., Pohl, J.B., Zelensky, P.K., Wang, D., Nitabach, M.N., Holmes, T.C., and White, B.H. (2006). Functional dissection of a neuronal network required for cuticle tanning and wing expansion in Drosophila. J. Neurosci. 26, 573-584. https://doi.org/10.1523/JNEUROSCI.3916-05.2006
- Melcher, C., and Pankratz, M.J. (2005). Candidate gustatory interneurons modulating feeding behavior in the Drosophila brain. PLoS Biol. 3, e305. https://doi.org/10.1371/journal.pbio.0030305
- Micchelli, C.A., and Perrimon, N. (2006). Evidence that stem cells reside in the adult Drosophila midgut epithelium. Nature 439, 475-479. https://doi.org/10.1038/nature04371
- Min, S., Chae, B., Jang, Y.H., Choi, S., Lee, S., Jeong, Y.T., Jones, W.D., Moon, S.J., Kim, Y.J., and Chung, J. (2016). Identification of a peptidergic pathway critical to satiety responses in Drosophila. Curr. Biol., in press.
- Nassel, D.R., and Winther, A.M. (2010). Drosophila neuropeptides in regulation of physiology and behavior. Prog. Neurobiol. 92, 42-104. https://doi.org/10.1016/j.pneurobio.2010.04.010
- Ohlstein, B., and Spradling, A. (2006). The adult Drosophila posterior midgut is maintained by pluripotent stem cells. Nature 439, 470-474. https://doi.org/10.1038/nature04333
- Park, J.H., and Kwon, J.Y. (2011). A systematic analysis of Drosophila gustatory receptor gene expression in abdominal neurons which project to the central nervous system. Mol. Cells 32, 375-381. https://doi.org/10.1007/s10059-011-0128-1
- Park, S., Sonn J.Y., Oh Y., Lim C., and Choe J. (2014). SIFamide and SIFamide receptor defines a novel neuropeptide signaling to promote sleep in Drosophila. Mol. Cells 37, 295-301. https://doi.org/10.14348/molcells.2014.2371
- Park, J.H., Chen, J., Jang, S., Ahn, T.J., Kang, K., Choi, M.S., and Kwon, J.Y. (2016). A subset of enteroendocrine cells is activated by amino acids in the Drosophila midgut. FEBS Lett., in press.
- Price, M.D., Merte, J., Nichols, R., Koladich, P.M., Tobe, S.S., and Bendena, W.G. (2002). Drosophila melanogaster flatline encodes a myotropin orthologue to Manduca sexta allatostatin. Peptides 23, 787-794. https://doi.org/10.1016/S0196-9781(01)00649-0
- Psichas, A., Reimann, F., and Gribble, F.M. (2015). Gut chemosensing mechanisms. J. Clin. Invest. 125, 908-917. https://doi.org/10.1172/JCI76309
- Reiher, W., Shirras, C., Kahnt, J., Baumeister, S., Isaac, R.E., and Wegener, C. (2011). Peptidomics and peptide hormone processing in the Drosophila midgut. J. Proteome Res. 10, 1881-1892. https://doi.org/10.1021/pr101116g
- Scopelliti, A., Cordero, J.B., Diao, F., Strathdee, K., White, B.H., Sansom, O.J., and Vidal, M. (2014). Local control of intestinal stem cell homeostasis by enteroendocrine cells in the adult Drosophila midgut. Curr. Biol. 24, 1199-1211. https://doi.org/10.1016/j.cub.2014.04.007
- Siviter, R.J., Coast, G.M., Winther, A.M., Nachman, R.J., Taylor, C.A., Shirras, A.D., Coates, D., Isaac, R.E., and Nassel, D.R. (2000). Expression and functional characterization of a Drosophila neuropeptide precursor with homology to mammalian preprotachykinin A. J. Biol. Chem. 275, 23273-23280. https://doi.org/10.1074/jbc.M002875200
- Song, W., Veenstra, J.A., and Perrimon, N. (2014). Control of lipid metabolism by tachykinin in Drosophila. Cell Rep. 9, 40-47. https://doi.org/10.1016/j.celrep.2014.08.060
- Vanderveken, M., and O'Donnell, M.J. (2014). Effects of diuretic hormone 31, drosokinin, and allatostatin A on transepithelial K(+) transport and contraction frequency in the midgut and hindgut of larval Drosophila melanogaster. Arch. Insect Biochem. Physiol. 85, 76-93. https://doi.org/10.1002/arch.21144
- Veenstra, J.A. (2009). Peptidergic paracrine and endocrine cells in the midgut of the fruit fly maggot. Cell Tissue Res. 336, 309-323. https://doi.org/10.1007/s00441-009-0769-y
- Veenstra, J.A., and Ida, T. (2014). More Drosophila enteroendocrine peptides: Orcokinin B and the CCHamides 1 and 2. Cell Tissue Res. 357, 607-621. https://doi.org/10.1007/s00441-014-1880-2
- Veenstra, J.A., Agricola, H.J., and Sellami, A. (2008). Regulatory peptides in fruit fly midgut. Cell Tissue Res. 334, 499-516. https://doi.org/10.1007/s00441-008-0708-3
- Wang, C., Guo, X., Dou, K., Chen, H., and Xi, R. (2015). Ttk69 acts as a master repressor of enteroendocrine cell specification in Drosophila intestinal stem cell lineages. Development 142, 3321-3331. https://doi.org/10.1242/dev.123208
- Wegener, C., and Veenstra, J.A. (2015). Chemical identity, function and regulation of enteroendocrine peptides in insects. Curr. Opin. Insect Sci. 11, 8-13. https://doi.org/10.1016/j.cois.2015.07.003
- Williamson, M., Lenz, C., Winther, A.M., Nassel, D.R., and Grimmelikhuijzen, C.J. (2001). Molecular cloning, genomic organization, and expression of a B-type (cricket-type) allatostatin preprohormone from Drosophila melanogaster. Biochem. Biophys. Res. Commun. 281, 544-550. https://doi.org/10.1006/bbrc.2001.4402
- Wu, Q., Wen, T., Lee, G., Park, J.H., Cai, H.N., and Shen, P. (2003). Developmental control of foraging and social behavior by the Drosophila neuropeptide Y-like system. Neuron 39, 147-161. https://doi.org/10.1016/S0896-6273(03)00396-9
- Zeng, X., and Hou, S.X. (2015). Enteroendocrine cells are generated from stem cells through a distinct progenitor in the adult Drosophila posterior midgut. Development 142, 644-653. https://doi.org/10.1242/dev.113357
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