The versatile stellate cell - More than just a space-filler

Journal of Insect Physiology

Volumn 58, Issue 4, 2012, Pages 467-472

  Dow, Julian A T ^a  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

Author keywords

Ion transport; Malpighian tubule; Neuropeptide; Stellate cell

Indexed keywords

CATION TRANSPORT PROTEIN; WATER;

CELL ORGANELLE; CHLORIDE; DATA SET; ION EXCHANGE; MEMBRANE; NUMERICAL MODEL; PEPTIDE; PLASMA;

ANIMAL; CYTOLOGY; INSECT; NEUROSECRETION; PHYSIOLOGY; PRENATAL DEVELOPMENT; REVIEW; TRANSPORT AT THE CELLULAR LEVEL;

ANIMALS; BIOLOGICAL TRANSPORT; CATION TRANSPORT PROTEINS; INSECTS; NEUROSECRETORY SYSTEMS; WATER;

HEXAPODA; VERTEBRATA;

EID: 84859432678     PISSN: 00221910     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jinsphys.2011.12.003     Document Type: Review

References (56)

1. Berridge M.J., Oschman J.L. A structural basis for fluid secretion by Malpighian tubules. Tissue & Cell 1969, 1:247-272.
2. Beyenbach K.W. Mechanism and regulation of electrolyte transport in Malpighian tubules. Journal of Insect Physiology 1995, 41:197-207.
3. Beyenbach K.W., Skaer H., Dow J.A.T. The developmental, molecular, and transport biology of Malpighian tubules. Annual Review of Entomology 2010, 55:351-374.
4. Bradley T.J., Stuart A.M., Satir P. The ultrastructure of the larval malpighian tubules of a saline-water mosquito. Tissue & Cell 1982, 14:759-773.
5. Brett C.L., Donowitz M., Rao R. Evolutionary origins of eukaryotic sodium/proton exchangers. American Journal of Physiology Cell Physiology 2005, 288:C223-239.
6. Cabrero P., Pollock V.P., Davies S.A., Dow J.A.T. A conserved domain of alkaline phosphatase expression in the Malpighian tubules of dipteran insects. Journal of Experimental Biology 2004, 207:3299-3305.
7. Campbell K., Casanova J., Skaer H. Mesenchymal-to-epithelial transition of intercalating cells in Drosophila renal tubules depends on polarity cues from epithelial neighbours. Mechanisms of Development 2010, 127:345-357.
8. Chapman R.F. The insects: structure and function 1982, Hodder & Stoughton, London. third ed.
9. Chintapalli V.R., Wang J., Dow J.A.T. Using FlyAtlas to identify better Drosophila models of human disease. Nature Genetics 2007, 39:715-720.
10. Coast G.M. Neuropeptides implicated in the control of diuresis in insects. Peptides 1996, 17:327-336.
11. Coast G.M. Intracellular ion measurements in Malpighian tubules of the house cricket: implications for the mode of action of diuretic kinins, Society for Experimental Biology Annual Main Meeting 2011 2011, Glasgow, UK, p. 61.
12. Coast G.M., Orchard I., Phillips J.E., Schooley D.A. Insect diuretic and antidiuretic hormones. Advances in Insect Physiology 2002, 29:279-409.
13. Day J.P., Wan S., Allan A.K., Kean L., Davies S.A., Gray J.V., Dow J.A.T. Identification of two partners from the bacterial Kef exchanger family for the apical plasma membrane V-ATPase of Metazoa. Journal of Cell Science 2008, 121:2612-2619.
14. Denholm B., Sudarsan V., Pasalodos-Sanchez S., Artero R., Lawrence P., Maddrell S., Baylies M., Skaer H. Dual origin of the renal tubules in Drosophila: mesodermal cells integrate and polarize to establish secretory function. Current Biology 2003, 13:1052-1057.
15. Dow J.A.T., Davies S.A. The Drosophila melanogaster Malpighian tubule. Advances in Insect Physiology 2001, 28:1-83.
16. Dow J.A.T., Davies S.A. Integrative physiology and functional genomics of epithelial function in a genetic model organism. Physiological Reviews 2003, 83:687-729.
17. Dow J.A.T., Kelly D.C., Davies S.A., Maddrell S.H.P., Brown D. A novel member of the major intrinsic protein family In Drosophila - are aquaporins involved in insect Malpighian (renal) tubule fluid secretion?. Journal of Physiology 1995, 489:P110-P111.
18. Dow J.A.T., Peacock J.M. Microelectrode evidence for the electrical isolation of goblet cavities of the middle midgut of Manduca sexta. Journal of Experimental Biology 1989, 143:101-114.
19. Harvey W.R., Cioffi M., Dow J.A.T., Wolfersberger M.G. Potassium ion transport ATPase in insect epithelia. Journal of Experimental Biology 1983, 106:91-117.
20. Harvey W.R., Cioffi M., Wolfersberger M.G. Portasomes as coupling factors in active ion transport and oxidative phosphorylation. American Zoologist 1981, 21:775-791.
21. Kaufmann N., Mathai J.C., Hill W.G., Dow J.A.T., Zeidel M.L., Brodsky J.L. Developmental expression and biophysical characterization of a Drosophila melanogaster aquaporin. American Journal of Physiology Cell Physiology 2005, 289:C397-C407.
22. Kerr M., Davies S.A., Dow J.A.T. Cell-specific manipulation of second messengers; a toolbox for integrative physiology in Drosophila. Current Biology 2004, 14:1468-1474.
23. Kersch, C.N., Pietrantonio, P.V., 2011. Mosquito Aedes aegypti (L.) leucokinin receptor is critical for in vivo fluid excretion post blood feeding. FEBS Letters in press.
24. Liu K., Tsujimoto H., Cha S.J., Agre P., Rasgon J.L. Aquaporin water channel AgAQP1 in the malaria vector mosquito Anopheles gambiae during blood feeding and humidity adaptation. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:6062-6066.
25. Lu H.L., Kersch C., Pietrantonio P.V. The kinin receptor is expressed in the Malpighian tubule stellate cells in the mosquito Aedes aegypti (L.): a new model needed to explain ion transport?. Insect Biochemistry & Molecular Biology 2011, 41:135-140.
26. Maddrell S.H.P. The fastest fluid-secreting cell known: the upper Malpighian tubule cell of Rhodnius. BioEssays 1991, 13:357-362.
27. Meulemans W., De Loof A. Transport of the cationic fluorochrome rhodamine 123 in an insect's Malpighian tubule: indications of a reabsorptive function of the secondary cell type. Journal of Cell Science 1992, 101:349-361.
28. Nelson N., Harvey W.R. Vacuolar and plasma membrane proton-adenosinetriphosphatases. Physiological Reviews 1999, 79:361-385.
29. O'Connor K., Beyenbach K.W. Two families of chloride channels in apical patches of stellate cells of Malpighian tubules of the yellow fever mosquito Aedes aegypti 2000, XXI International congress of entomology, Foz do Iguassu, Brazil, p. 626.
30. O'Donnell M.J., Dow J.A.T., Huesmann G.R., Tublitz N.J., Maddrell S.H.P. Separate control of anion and cation transport in malpighian tubules of Drosophila melanogaster. Journal of Experimental Biology 1996, 199:1163-1175.
31. O'Donnell M.J., Rheault M.R., Davies S.A., Rosay P., Harvey B.J., Maddrell S.H.P., Kaiser K., Dow J.A.T. Hormonally controlled chloride movement across Drosophila tubules is via ion channels in stellate cells. American Journal of Physiology 1998, 274:R1039-R1049.
32. Pantel J. Signification des " glandes annexes" intestinales des larves des " Ptychopteridae" et observations sur les tubes de Malpighi de ces Nematoceres (larves et adultes). La Cellule 1914, 29:393-429.
33. +-ATPase expression patterns in the osmoregulatory organs of larval and adult mosquito Aedes aegypti. Journal of Experimental Biology 2006, 209:4638-4651.
34. Patrick M.L., Gill S.S. Does Na+/K+ ATPase and/or V-type H+ ATPase drive ion regulation in salt-tolerant mosquito larvae?. Comparative Biochemistry and Physiology - Part A: Molecular & Integrative Physiology 2002, 134(Suppl1):S70.
35. Piermarini P.M., Grogan L.F., Lau K., Wang L., Beyenbach K.W. A SLC4-like anion exchanger from renal tubules of the mosquito (Aedes aegypti): evidence for a novel role of stellate cells in diuretic fluid secretion. American Journal of Physiology Regulatory Integrative & Comparative Physiology 2010, 298:R642-R660.
36. Poulson D.F. Histogenesis, organogenesis and differentiation in the embryo of Drosophila melanogaster Meigen. Biology of Drosophila 1950, 168-274. John Wiley & Sons, New York. M. Demerec (Ed.).
37. Radford J.C., Davies S.A., Dow J.A. Systematic G-protein-coupled receptor analysis in Drosophila melanogaster identifies a leucokinin receptor with novel roles. Journal of Biological Chemistry 2002, 277:38810-38817.
38. Radford J.C., Terhzaz S., Cabrero P., Davies S.A., Dow J.A. Functional characterisation of the Anopheles leucokinins and their cognate G-protein coupled receptor. Journal of Experimental Biology 2004, 207:4573-4586.
39. Satmary W.M., Bradley T.J. The distribution of cell types in the Malpighian tubules of Aedes taeniorhynchus (Wiedemann) (Diptera: Culicidae). International Journal of Insect Morphology & Embryology 1984, 13:209-214.
40. Schindler E. Beitraege zur Kenntuis der Malpighi'schen Gefaesse der Insecten. Zeitschrift für wissenschaftliche Zoologie 1878, 30:587-660.
41. Singh S.R., Hou S.X. Multipotent stem cells in the Malpighian tubules of adult Drosophila melanogaster. Journal of Experimental Biology 2009, 212:413-423.
42. Singh S.R., Liu W., Hou S.X. The adult Drosophila Malpighian tubules are maintained by multipotent stem cells. Cell Stem Cell 2007, 1:191-203.
43. Skaer H. The alimentary canal. The Development of Drosophila melanogaster 1993, 941-1012. Cold Spring Harbor Press, Cold Spring Harbor. M. Bate, A. Martinez Arias (Eds.).
44. Sözen, M.A., 1996. Mapping domains of gene expression in the Malpighian tubule of Drosophila melanogaster by enhancer trapping. University of Glasgow.
45. Sözen M.A., Armstrong J.D., Yang M.Y., Kaiser K., Dow J.A.T. Functional domains are specified to single-cell resolution in a Drosophila epithelium. Proceedings of the National Academy of Sciences of the United States of America 1997, 94:5207-5212.
46. Taylor H.H. The fine structure of the type 2 cells in the Malpighian tubules of the stick insect, Carausius morosus. Zeitschrift für Zellforschung und mikroskopische Anatomie 1971, 122:411-424.
47. Thomas J.E., Rylett C.M., Carhan A., Bland N.D., Bingham R.J., Shirras A.D., Turner A.J., Isaac R.E. Drosophila melanogaster NEP2 is a new soluble member of the neprilysin family of endopeptidases with implications for reproduction and renal function. Biochemical Journal 2005, 386:357-366.
48. Torrie L.S., Radford J.C., Southall T.D., Kean L., Dinsmore A.J., Davies S.A., Dow J.A.T. Resolution of the insect ouabain paradox. Proceedings of the National Academy of Sciences of the United States of America 2004, 101:13689-13693.
49. Veenstra J.A., Pattillo J.M., Petzel D.H. A single cDNA encodes all three Aedes leucokinins, which stimulate both fluid secretion by the Malpighian tubules and hindgut contractions. Journal of Biological Chemistry 1997, 272:10402-10407.
50. Wall B.J., Oschmann J.L., Schmidt B.A. Morphology & function of the Malpighian tubules and associated structures in the cockroach Periplaneta americana. Journal of Morphology 1975, 146:265-306.
51. Wang J., Kean L., Yang J., Allan A.K., Davies S.A., Herzyk P., Dow J.A.T. Function-informed transcriptome analysis of Drosophila renal tubule. Genome Biology 2004, 5:R69.
52. Weng X.H., Piermarini P.M., Yamahiro A., Yu M.J., Aneshansley D.J., Beyenbach K.W. Gap junctions in Malpighian tubules of Aedes aegypti. Journal of Experimental Biology 2008, 211:409-422.
53. Wessing A., Eichelberg D. Malpighian tubules, rectal papillae and excretion. The genetics and biology of Drosophila 1978, 1-42. Academic Press, London. A. Ashburner, T.R.F. Wright (Eds.).
54. Wessing A., Zierold K., Polenz A. Stellate cells in the Malpighian tubules of Drosophila hydei and D. Melanogaster larvae (Insecta, Diptera). Zoomorphology 1999, 119:63-71.
55. Wigglesworth V.B. The principles of insect physiology 1939, Methuen, London.
56. Xiang M., Harvey W.R., Heilig C.W., Li L., Price D.A., Linser P.J. Characterization of AgNHA2, the second isoform of the cation/proton antiporter from Anopheles gambiae, Society for Experimental Biology Annual Main Meeting, 2011 2011, Society for Experimental Biology, Glasgow, UK, p. 64.