Two ligands signal through the Drosophila PDGF/VEGF receptor to ensure proper salivary gland positioning

Mechanisms of Development

Volumn 124, Issue 6, 2007, Pages 441-448

  Harris, Katherine E ^a   Schnittke, Nikolai ^a   Beckendorf, Steven K ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Cell migration; Drosophila; PDGF; Pvf1; Pvf2; Pvf3; Pvr; Salivary gland; VEGF

Indexed keywords

PLATELET DERIVED GROWTH FACTOR RECEPTOR; VASCULOTROPIN RECEPTOR;

ARTICLE; CELL MIGRATION; DROSOPHILA; GENE EXPRESSION; GENE MUTATION; NONHUMAN; PRIORITY JOURNAL; SALIVARY GLAND;

ANIMALS; DROSOPHILA; DROSOPHILA PROTEINS; EGG PROTEINS; LIGANDS; MORPHOGENESIS; RECEPTOR PROTEIN-TYROSINE KINASES; SALIVARY GLANDS; VASCULAR ENDOTHELIAL GROWTH FACTORS;

EID: 34248672527     PISSN: 09254773     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mod.2007.03.003     Document Type: Article

References (29)

1. Andrew D.J., Henderson K.D., and Seshaiah P. Salivary gland development in Drosophila melanogaster. Mech. Dev. 92 (2000) 5-17
2. Bonasio R., Scimone M.L., Schaerli P., Grabie N., Lichtman A.H., and von Andrian U.H. Clonal deletion of thymocytes by circulating dendritic cells homing to the thymus. Nat. Immunol. 7 (2006) 1092-1100
3. Bradley P.L., Haberman A.S., and Andrew D.J. Organ formation in Drosophila: specification and morphogenesis of the salivary gland. Bioessays 23 (2001) 901-911
4. Bradley P.L., Myat M.M., Comeaux C.A., and Andrew D.J. Posterior migration of the salivary gland requires an intact visceral mesoderm and integrin function. Dev. Biol. 257 (2003) 249-262
5. Bruckner K., Kockel L., Duchek P., Luque C.M., Rorth P., and Perrimon N. The PDGF/VEGF receptor controls blood cell survival in Drosophila. Dev. Cell 7 (2004) 73-84
6. Chandrasekaran V., and Beckendorf S.K. Senseless is necessary for the survival of embryonic salivary glands in Drosophila. Development 130 (2003) 4719-4728
7. Cho N.K., Keyes L., Johnson E., Heller J., Ryner L., Karim F., and Krasnow M.A. Developmental control of blood cell migration by the Drosophila VEGF pathway. Cell 108 (2002) 865-876
8. Duchek P., Somogyi K., Jekely G., Beccari S., and Rorth P. Guidance of cell migration by the Drosophila PDGF/VEGF receptor. Cell 107 (2001) 17-26
9. Fessler L.I., Nelson R.E., and Fessler J.H. Drosophila extracellular matrix. Methods Enzymol. 245 (1994) 271-294
10. Harland R.M. In situ hybridization: an improved whole-mount method for Xenopus embryos. Methods Cell Biol. 36 (1991) 685-695
11. Harris, K.E., Beckendorf, S.K. 2007. Different Wnt signals act through the Frizzled and RYK receptors during Drosophila salivary gland migration. Development, in press.
12. Heidaran M.A., Pierce J.H., Yu J.C., Lombardi D., Artrip J.E., Fleming T.P., Thomason A., and Aaronson S.A. Role of alpha beta receptor heterodimer formation in beta platelet-derived growth factor (PDGF) receptor activation by PDGF-AB. J. Biol. Chem. 266 (1991) 20232-20237
13. Ishimaru S., Ueda R., Hinohara Y., Ohtani M., and Hanafusa H. PVR plays a critical role via JNK activation in thorax closure during Drosophila metamorphosis. EMBO J. 23 (2004) 3984-3994
14. Kerman B.E., Cheshire A.M., and Andrew D.J. From fate to function: the Drosophila trachea and salivary gland as models for tubulogenesis. Differentiation 74 (2006) 326-348
15. Kolesnikov T., and Beckendorf S.K. NETRIN and SLIT guide salivary gland migration. Dev. Biol. 284 (2005) 102-111
16. Kondo T., Konishi F., Inui H., and Inagami T. Differing signal transductions elicited by three isoforms of platelet-derived growth factor in vascular smooth muscle cells. J. Biol. Chem. 268 (1993) 4458-4464
17. Lepisto J., Peltonen J., Vaha-Kreula M., Niinikoski J., and Laato M. Platelet-derived growth factor isoforms PDGF-AA, -AB and -BB exert specific effects on collagen gene expression and mitotic activity of cultured human wound fibroblasts. Biochem. Biophys. Res. Commun. 209 (1995) 393-399
18. Luster A.D., Alon R., and von Andrian U.H. Immune cell migration in inflammation: present and future therapeutic targets. Nat. Immunol. 6 (2005) 1182-1190
19. Macias A., Romero N.M., Martin F., Suarez L., Rosa A.L., and Morata G. PVF1/PVR signaling and apoptosis promotes the rotation and dorsal closure of the Drosophila male terminalia. Int. J. Dev. Biol. 48 (2004) 1087-1094
20. McDonald J.A., Pinheiro E.M., and Montell D.J. PVF1, a PDGF/VEGF homolog, is sufficient to guide border cells and interacts genetically with Taiman. Development 130 (2003) 3469-3478
21. Montell D.J. The social lives of migrating cells in Drosophila. Curr. Opin. Genet. Dev. 16 (2006) 374-383
22. Nelson R.E., Fessler L.I., Takagi Y., Blumberg B., Keene D.R., Olson P.F., Parker C.G., and Fessler J.H. Peroxidasin: a novel enzyme-matrix protein of Drosophila development. Embo. J. 13 (1994) 3438-3447
23. Olofsson B., and Page D.T. Condensation of the central nervous system in embryonic Drosophila is inhibited by blocking hemocyte migration or neural activity. Dev. Biol. 279 (2005) 233-243
24. Rosin D., Schejter E., Volk T., and Shilo B.Z. Apical accumulation of the Drosophila PDGF/VEGF receptor ligands provides a mechanism for triggering localized actin polymerization. Development 131 (2004) 1939-1948
25. Tautz D., and Pfeifle C. A non-radioactive in situ hybridization method for the localization of specific RNAs in Drosophila embryos reveals translational control of the segmentation gene hunchback. Chromosoma 98 (1989) 81-85
26. Tessier-Lavigne M., and Goodman C.S. The molecular biology of axon guidance. Science 274 (1996) 1123-1133
27. Vining M.S., Bradley P.L., Comeaux C.A., and Andrew D.J. Organ positioning in Drosophila requires complex tissue-tissue interactions. Dev. Biol. 287 (2005) 19-34
28. Wood W., Faria C., and Jacinto A. Distinct mechanisms regulate hemocyte chemotaxis during development and wound healing in Drosophila melanogaster. J. Cell Biol. 173 (2006) 405-416
29. Zhou B. Salivary Determination and Transcriptional Control of Fork Head in Drosophila melanogaster (1995), University of California, Berkeley pp. 220