Making a zebrafish kidney: A tale of two tubes

Trends in Cell Biology

Volumn 13, Issue 7, 2003, Pages 357-365

  Drummond, Iain ^a  

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANGIOGENESIS; BLOOD FILTER; BLOOD FLOW; BLOOD VESSEL DIAMETER; BRANCHING MORPHOGENESIS; CELL ACTIVITY; CELL ADHESION; CELL JUNCTION; CELL POLARITY; CELL SHAPE; CENTRIOLE; DEVELOPMENTAL STAGE; DISEASE MODEL; EPITHELIUM CELL; FUNCTIONAL ANATOMY; GENE EXPRESSION; GENE FUNCTION; GENETIC ANALYSIS; GLOMERULUS BASEMENT MEMBRANE; GLOMERULUS CAPILLARY; HUMAN; ION TRANSPORT; KIDNEY BLOOD VESSEL; KIDNEY CIRCULATION; KIDNEY DEVELOPMENT; KIDNEY EPITHELIUM; KIDNEY FUNCTION; KIDNEY POLYCYSTIC DISEASE; KIDNEY TUBULE; MOLECULAR EVOLUTION; NEPHRON; NONHUMAN; OSMOREGULATION; PATHOPHYSIOLOGY; PODOCYTE; PRIMORDIUM; PRIORITY JOURNAL; PROCESS MODEL; REVIEW; SEQUENCE HOMOLOGY; SOLUTE; SPECIES COMPARISON; TRANSCRIPTION REGULATION; VASCULARIZATION; WATER TRANSPORT; ZEBRA FISH;

DANIO RERIO; GLOMERULUS; GOES;

EID: 0037756725     PISSN: 09628924     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0962-8924(03)00124-7     Document Type: Review

References (74)

1. Vize, P. et al. (2002) The Kidney from Normal Development to Congenital Diseases, Academic Press.
2. Drummond I.A., et al. Early development of the zebrafish pronephros and analysis of mutations affecting pronephric function. Development. 125:1998;4655-4667.
3. Serluca F.C., Fishman M.C. Pre-pattern in the pronephric kidney field of zebrafish. Development. 128:2001;2233-2241.
4. Kimmel C.B., et al. Stages of embryonic development of the zebrafish. Dev. Dyn. 203:1995;253-310.
5. Horsfield J., et al. Cadherin-17 is required to maintain pronephric duct integrity during zebrafish development. Mech. Dev. 115:2002;15-26.
6. Dahl U., et al. Genetic dissection of cadherin function during nephrogenesis. Mol. Cell. Biol. 22:2002;1474-1487.
7. Seldin, D.W. and Giebisch, G.H. (1992) The Kidney: Physiology and Pathophysiology, Raven Press.
8. Yeaman C., et al. Cell polarity: versatile scaffolds keep things in place. Curr. Biol. 9:1999;R515-R517.
9. Saxén, L. (1987) Organogenesis of the Kidney, Cambridge University Press.
10. Bouchard M., et al. Nephric lineage specification by Pax2 and Pax8. Genes Dev. 16:2002;2958-2970.
11. Torres M., et al. Pax-2 controls multiple steps of urogenital development. Development. 121:1995;4057-4065.
12. Krauss, S. et al. (1991) Expression of the zebrafish paired box gene pax [zf-b] during early neurogenesis. Development 113, 1193-1206.
13. Majumdar A., et al. Zebrafish no isthmus reveals a role for pax2.1 in tubule differentiation and patterning events in the pronephric primordia. Development. 127:2000;2089-2098.
14. Yang Y., et al. WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis. Am. J. Pathol. 154:1999;181-192.
15. Briscoe J., et al. A homeodomain protein code specifies progenitor cell identity and neuronal fate in the ventral neural tube. Cell. 101:2000;435-445.
16. Schwarz M., et al. Spatial specification of mammalian eye territories by reciprocal transcriptional repression of Pax2 and Pax6. Development. 127:2000;4325-4334.
17. Li J.Y., Joyner A.L. Otx2 and Gbx2 are required for refinement and not induction of mid-hindbrain gene expression. Development. 128:2001;4979-4991.
18. McLaughlin K.A., et al. Notch regulates cell fate in the developing pronephros. Dev. Biol. 227:2000;567-580.
19. Smithers L., et al. Sequence and embryonic expression of deltaC in the zebrafish. Mech. Dev. 90:2000;119-123.
20. Pavenstadt H., et al. Cell biology of the glomerular podocyte. Physiol. Rev. 83:2003;253-307.
21. Majumdar A., Drummond I.A. Podocyte differentiation in the absence of endothelial cells as revealed in the zebrafish avascular mutant, cloche. Dev. Genet. 24:1999;220-229.
22. Kimmel C.B., et al. Origin and organization of the zebrafish fate map. Development. 108:1990;581-594.
23. Hammerschmidt M., et al. Genetic analysis of dorsoventral pattern formation in the zebrafish: requirement of a BMP-like ventralizing activity and its dorsal repressor. Genes Dev. 10:1996;2452-2461.
24. Hammerschmidt M., et al. dino and mercedes, two genes regulating dorsal development in the zebrafish embryo. Development. 123:1996;95-102.
25. Neave B., et al. A graded response to BMP-4 spatially coordinates patterning of the mesoderm and ectoderm in the zebrafish. Mech. Dev. 62:1997;183-195.
26. Nikaido M., et al. Conservation of BMP signaling in zebrafish mesoderm patterning. Mech. Dev. 61:1997;75-88.
27. Mullins M.C., et al. Genes establishing dorsoventral pattern formation in the zebrafish embryo: the ventral specifying genes. Development. 123:1996;81-93.
28. Nguyen V.H., et al. Ventral and lateral regions of the zebrafish gastrula, including the neural crest progenitors, are established by a bmp2b/swirl pathway of genes. Dev. Biol. 199:1998;93-110.
29. Kishimoto Y., et al. The molecular nature of zebrafish swirl: BMP2 function is essential during early dorsoventral patterning. Development. 124:1997;4457-4466.
30. Hild M., et al. The smad5 mutation somitabun blocks Bmp2b signaling during early dorsoventral patterning of the zebrafish embryo. Development. 126:1999;2149-2159.
31. Payne T.L., et al. Functional characterization and genetic mapping of alk8. Mech. Dev. 100:2001;275-289.
32. Mintzer K.A., et al. Lost-a-fin encodes a type I BMP receptor, Alk8, acting maternally and zygotically in dorsoventral pattern formation. Development. 128:2001;859-869.
33. Bauer H., et al. The type I serine/threonine kinase receptor Alk8/Lost-a-fin is required for Bmp2b/7 signal transduction during dorsoventral patterning of the zebrafish embryo. Development. 128:2001;849-858.
34. Weinstein B.M., et al. Hematopoietic mutations in the zebrafish. Development. 123:1996;303-309.
35. Detrich H.W. 3rd, et al. Intraembryonic hematopoietic cell migration during vertebrate development. Proc. Natl. Acad. Sci. U. S. A. 92:1995;10713-10717.
36. Gering M., et al. The SCL gene specifies haemangioblast development from early mesoderm. EMBO J. 17:1998;4029-4045.
37. Zhong T.P., et al. Gridlock signalling pathway fashions the first embryonic artery. Nature. 414:2001;216-220.
38. Armstrong P.B. The embryonic origin of function in the pronephros through differentiation and parenchyma-vascular association. Am. J. Anat. 51:1932;157-188.
39. Tytler P. Morphology of the pronephros of the juvenile brown trout, Salmo trutta. J. Morphol. 195:1988;189-204.
40. Drummond I.A. The zebrafish pronephros: a genetic system for studies of kidney development. Pediatr. Nephrol. 14:2000;428-435.
41. Pham V.N., et al. Isolation and expression analysis of three zebrafish angiopoietin genes. Dev. Dyn. 221:2001;470-474.
42. Majumdar A., Drummond I.A. The zebrafish floating head mutant demonstrates podocytes play an important role in directing glomerular differentiation. Dev. Biol. 222:2000;147-157.
43. Shalaby F., et al. Failure of blood-island formation and vasculogenesis in Flk-1-deficient mice. Nature. 376:1995;62-66.
44. Ferrara N., et al. Heterozygous embryonic lethality induced by targeted inactivation of the VEGF gene. Nature. 380:1996;439-442.
45. Carmeliet P., et al. Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele. Nature. 380:1996;435-439.
46. Fouquet B., et al. Vessel patterning in the embryo of the zebrafish: guidance by notochord. Dev. Biol. 183:1997;37-48.
47. Sehnert A.J., et al. Cardiac troponin T is essential in sarcomere assembly and cardiac contractility. Nat. Genet. 31:2002;106-110.
48. Rottbauer W., et al. Growth and function of the embryonic heart depend upon the cardiac-specific L-type calcium channel alpha1 subunit. Dev. Cell. 1:2001;265-275.
49. Serluca F.C., et al. Endothelial signaling in kidney morphogenesis: a role for hemodynamic forces. Curr. Biol. 12:2002;492-497.
50. Hove J.R., et al. Intracardiac fluid forces are an essential epigenetic factor for embryonic cardiogenesis. Nature. 421:2003;172-177.
51. Calvet J.P., Grantham J.J. The genetics and physiology of polycystic kidney disease. Semin. Nephrol. 21:2001;107-123.
52. Pazour G.J., et al. Chlamydomonas IFT88 and its mouse homologue, polycystic kidney disease gene tg737, are required for assembly of cilia and flagella. J. Cell Biol. 151:2000;709-718.
53. Taulman P.D., et al. Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia. Mol. Biol. Cell. 12:2001;589-599.
54. Yoder B.K., et al. Polaris, a protein disrupted in orpk mutant mice, is required for assembly of renal cilium. Am. J. Physiol. Renal Physiol. 282:2002;F541-F552.
55. Barr M.M., et al. The Caenorhabditis elegans autosomal dominant polycystic kidney disease gene homologs lov-1 and pkd-2 act in the same pathway. Curr. Biol. 11:2001;1341-1346.
56. Qin H., et al. An autosomal recessive polycystic kidney disease gene homolog is involved in intraflagellar transport in C. elegans ciliated sensory neurons. Curr. Biol. 11:2001;457-461.
57. Morgan D., et al. Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle. Hum. Mol. Genet. 11:2002;3345-3350.
58. Pazour G.J., et al. Polycystin-2 localizes to kidney cilia and the ciliary level is elevated in orpk mice with polycystic kidney disease. Curr. Biol. 12:2002;R378-R380.
59. Yoder B.K., et al. The polycystic kidney disease proteins, polycystin-1, polycystin-2, polaris, and cystin, are co-localized in renal cilia. J. Am. Soc. Nephrol. 13:2002;2508-2516.
60. Tabin C.J., Vogan K.J. A two-cilia model for vertebrate left-right axis specification. Genes Dev. 17:2003;1-6.
61. Pennekamp P., et al. The ion channel polycystin-2 is required for left-right axis determination in mice. Curr. Biol. 12:2002;938-943.
62. Morgan D., et al. Inversin, a novel gene in the vertebrate left-right axis pathway, is partially deleted in the inv mouse. Nat. Genet. 20:1998;149-156.
63. Pazour G.J., et al. The intraflagellar transport protein, IFT88, is essential for vertebrate photoreceptor assembly and maintenance. J. Cell Biol. 157:2002;103-113.
64. Praetorius H.A., Spring K.R. Bending the MDCK cell primary cilium increases intracellular calcium. J. Membr. Biol. 184:2001;71-79.
65. Nauli S.M., et al. Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells. Nat. Genet. 33:2003;129-137.
66. Liu S., et al. A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development. 129:2002;5839-5846.
67. Fry A.M. The Nek2 protein kinase: a novel regulator of centrosome structure. Oncogene. 21:2002;6184-6194.
68. Mahjoub M.R., et al. The FA2 gene of Chlamydomonas encodes a NIMA family kinase with roles in cell cycle progression and microtubule severing during deflagellation. J. Cell Sci. 115:2002;1759-1768.
69. Sun Z., Hopkins N. vhnf1, the MODY5 and familial GCKD-associated gene, regulates regional specification of the zebrafish gut, pronephros, and hindbrain. Genes Dev. 15:2001;3217-3229.
70. Froguel P., Velho G. Molecular genetics of maturity-onset diabetes of the young. Trends Endocrinol. Metab. 10:1999;142-146.
71. Dutcher S.K. Flagellar assembly in two hundred and fifty easy-to-follow steps. Trends Genet. 11:1995;398-404.
72. Ostrowski L.E., et al. A proteomic analysis of human cilia: identification of novel components. Mol. Cell Proteomics. 1:2002;451-465.
73. James R.G., Schultheiss T.M. Patterning of the avian intermediate mesoderm by lateral plate and axial tissues. Dev. Biol. 253:2003;109-124.
74. Mauch T.J., et al. Signals from trunk paraxial mesoderm induce pronephros formation in chick intermediate mesoderm. Dev. Biol. 220:2000;62-75.