Role of endothelin in the human craniofacial morphogenesis

Journal of Craniofacial Genetics and Developmental Biology

Volumn 18, Issue 4, 1998, Pages 183-194

  Barni, Tullio ^a   Fantoni, Guido ^a   Gloria, Luciana ^a   Maggi, Mario ^a   Peri, Alessandro ^a   Balsi, Emanuela ^a   Grappone, Cecilia ^a   Vannelli, Gabriella Barbara ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

Author keywords

Craniofacial development; Endothelin; Human; Morphogenesis

Indexed keywords

ENDOTHELIN; ENDOTHELIN 1; ENDOTHELIN A RECEPTOR; ENDOTHELIN B RECEPTOR; ENDOTHELIN RECEPTOR; MESSENGER RNA; ONCOPROTEIN; PEPTIDE; PROTEIN C FOS; THYMIDINE;

ANIMAL MODEL; ARTICLE; BONE DEVELOPMENT; BRANCHIAL ARCH; CONTROLLED STUDY; CRANIOFACIAL DEVELOPMENT; EPITHELIUM CELL; FETUS; FETUS DEVELOPMENT; GENE EXPRESSION; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; JAW; MANDIBLE; MESENCHYME; MORPHOGENESIS; MOUSE; MOUTH MUCOSA; NONHUMAN; PHARYNX; PRIORITY JOURNAL;

BONE AND BONES; CRANIOFACIAL ABNORMALITIES; ENDOTHELIN-1; ENDOTHELIN-3; GENE EXPRESSION; HUMANS; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; JAW; MORPHOGENESIS; MOUTH MUCOSA; OROPHARYNX; OSTEONECTIN; PEPTIDES, CYCLIC; PROTO-ONCOGENE PROTEINS C-FOS; RECEPTOR, ENDOTHELIN A; RECEPTOR, ENDOTHELIN B; RECEPTORS, ENDOTHELIN; TONGUE;

EID: 0032462059     PISSN: 02704145     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (38)

1. ADACHI M, YANG YY, FURUICHI Y, MIYAMOTO C: Cloning and characterization of cDNA encoding human A-type endothelin receptor. Biochem Biophys Res Comm 180:1265-1272, 1991.
2. BALLING R, MUTTER G, GRUSS P, KESSEL M: Craniofacial abnormalities induced by ectopic expression of the homeobox gene Hox-1.1 in transgenic mice. Cell 58:337-347, 1989.
3. BARNI T, VANNELLI GB, SADRI R, PUPILLI C, GHIANDI P, RIZZO M, SELLI C, SERIO M, FIORELLI G: Insulin-like growth factor-I (IGF-I) and its binding protein IGFBP-4 in human hyperplastic tissue: Gene expression and its cellular localization. J Clin Endocrinol Metab 78:778-783, 1994.
4. BARNI T, MAGGI M, FANTONI G, SERIO M, TOLLARO I, GLORIA L, VANNELLI GB: Identification and localization of endothelin-1 and its receptors in human fetal jaws. Dev Biol 169:373-377, 1995.
5. CHAI Y, MAH A, CRONHIN C, GROFF S, BRINGAS, JR P, LE T, SANTOS V, SLAVKIN HC: Specific transforming growth factor-β subtypes regulate embryonic mouse Meckel's cartilage and tooth development. Dev Biol 162:85-103, 1994.
6. CHISAKA O, CAPECCHI MR: Regionally restricted developmental defects resulting from targeted disruption of the mouse homeobox gene Hox-1.5. Nature 350:473-479, 1991.
7. CLOUTHIER DE, HOSODA K, RICHARDSON JA, WILLIAMS SC, YANAGISAWA H, KUWAKI T, KUMADA M, HAMMER RE, YANAGISAWA M: Cranial and cardiac neural crest defects in endothelin-A receptor-deficient mice. Development 125:813-824, 1998.
8. FRANGIONI G, BORGIOLI G: Polystyrene embedding and spreading of sections at lower temperature. Stain Technol 57:256-257, 1982.
9. GENDRON-MAGUIRE M, MALLO M, ZHANG M, GRIDLEY T: Hoxa-2 mutant mice exhibit homeotic transformation of skeletal elements derived from cranial neural crest. Cell 75:1317-1331, 1993.
10. KESSEL M, GRUSS P: Homeotic transformation of murine vertebrae and concomitant alteration of Hox codes induced by retinoic acid. Cell 67:89-104, 1991.
11. KOMURO I, KURIHARA H, SUGIYAMA T, TAKAKU F, YAZAKI Y: Endothelin stimulates c-fos and c-myc expression and proliferation of vascular smooth muscle cells. FEBS Lett 238:249-252, 1988.
12. KURIHARA Y, KURIHARA H, SUZUKI H, KODAMA T, MAEMURA K, NAGAI R, ODA H, KUWAKI T, CAO WH, KAMADA N, JISHAGE K, OUCHI Y, AZUMA S, TOYODA Y, ISHIKAWA T, KUMADA M, YAZAKI Y: Elevated blood pressure and craniofacial abnormalities in mice deficient in endothelin-1. Nature 368:703-710, 1994.
13. MAGGI M, VANNELLI GB, PERI A, BRANDI ML, FANTONI G, GIANNINI S, TORRISI C, GUARDABASSO V, BARNI T, TOSCANO V, MASSI G, SERIO M: Immunolocalization, binding and biological activity of endothelin in rabbit uterus: effect of ovarian steroids. Am J Physiol 260:E292-E305, 1991.
14. MALLAT A, FOUASSIER F, PREAUX AM, SERRADEIL-LE GAL C, RAUFASTE D, ROSEMBAUM J, DUMEAUX D, JOUNEAUX C, MAVIER P, LOTERSZTAJN S: Growth inhibitory properties of endothelin-1 in human hepatic myofibroblastic Ito cells: an endothelin B receptor-mediated pathway. J Clin Invest 96:42-49, 1995.
15. MANCINA R, BARNI T, CALOGERO AE, FILIPPI S, AMERINI S, PERI A, SUSINI T, VANNELLI GB, BURRELLO N, FORTI G, AND MAGGI M: Identification, characterization and biological activity of endothelin receptors in human ovary. J Clin Endocrinol Metab 82:4122-4129, 1997.
16. MASAKI T, YANAGISAWA M, GOTO K: Physiology and pharmacology of endothelins. Med Res Rev 12:391-421, 1992.
17. MINA M, GLUHAK J, UPHOLT WB, KOLLAR EJ, ROGERS B: Experimental analysis of Msx-1 and Msx-2 gene expression during chick mandibular morphogenesis. Dev Dyn 202:195-214, 1995.
18. MUENKE M, SCHELL U, HEHR A, ROBIN NH, LOSKEN HW, SCHINZEL A, PULLEYN LJ, RUTLAND P, REARDON W, MALCOLM S, WINTER RM: A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome. Nature Genet 8:269-274, 1994.
19. NELSON JB, HEDICAN SP, GEORGE DJ, REDDI AH, PIANTADOSI S, EISENBERGER MA, SIMONS JW: Identification of endothelin-1 in the pathophysiology of metastatic adenocarcinoma of the prostate. Nature Med 1:944-949, 1995.
20. OSUMI-YAMASHITA N, NOJI S, NOHNO T, KOYAMA E, DOI H, ETO K, TANIGUCHI S: Expression of retinoic acid receptor genes in neural crest-derived cells during mouse facial development. FEBS Lett 1:71-74, 1990.
21. 125I-epidermal growth factor binding to embryonic tooth and other embryonic tissues at different developmental stages. Dev Biol 120:86-197, 1987.
22. PERI A, FANTONI G, GRANCHI S, VANNELLI GB, BARNI T, AMERINI S, PUPILLI C, BARBAGLI G, FORTI G, SERIO M, MAGGI M: Gene expression of endothelin-1, endothelin-converting enzyme-1 and endothelin receptors in human epididymis. J Clin Endocrinol Metab 82:3797-3806, 1997.
23. REARDON W, WINTER RM, RUTLAND P, PULLEYN LJ, JONES BM, MALCOLM S: Mutations in the fibroblast growth factor receptor-2 gene cause Crouzon syndrome. Nature Genet 8:98-103, 1994.
24. ROUSSEAU F, BONAVENTURE, J, LEGEAI-MALLET L, PELET A, ROZET JM, MAROTEAUX P, LE MERRER M, MUNNICH A: Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia. Nature 371:252-254, 1994.
25. RUTLAND P, PULLEYN LJ, REARDON W, BARAITSER M, HAYWARD R, JONES B, MALCOLM S, WINTER RM, OLDRIDGE M, SLANEY SF, POOLE MD, WILKIE AOM: Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. Nature Genet 9:173-176, 1995.
26. SAKURAI T, YANAGISAWA M, TAKUWA H, MIYAZAKI T, KIMURA S, GOTO K, MASAKI T: Cloning of a cDNA encoding a non-isopeptide-selective subtype of the endothelin receptor. Nature 348:732-734, 1990.
27. SCHORLE H, MEIER P, BUCHERT M, JAENISCH R, MITCHELL PJ: Transcription factor AP-2 essential for cranial closure and craniofacial development. Nature 381:235-238, 1996.
28. SHIANG R, THOMPSON LM, ZHU YZ, CHURCH DM, FIELDER TJ, BOCIAN M, WINOKUR ST, WASMUTH JJ: Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78:335-342, 1994.
29. SIMONSON MS, WANN S, MENÉ P, DUBYAK GR, KESTER M, NAKAZATO Y, SEDOR JR, DUNN MJ: Endothelin stimulates phospholipase C, Na/H exchange, c-fos expression, and mitogenesis in rat mesangial cells. J Clin Invest 83:708-712, 1989.
30. SIMONSON MS: Endothelins: multifunctional renal peptides. Physiol Rev 73:375-411, 1993.
31. TAKUWA Y, MASAKI T, YAMASHITA K: The effects of the endothelin family peptides on cultured osteoblastic cells from rat calvariae. Biochem Biophys Res Comm 170:998-1005, 1990.
32. WANG JABS E, LI X, SCOTT AF, MEYERS G, CHEN W, ECCLES M, MAO J, CHARNAS LR, JACKSON CE, JAYE M: Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nature Genet 8:275-279, 1994.
33. WANG ZQ, OVITT C, GRIGORIADIS AE, MOHLE-STEINLEIN U, RUTHER U, WAGNER EF: Bone and hematopoietic defects in mice lacking c-fos. Nature 360:741-745, 1992.
34. WILKIE AOM, SLANEY SF, OLDRIDGE M, POOLE MD, ASHWORTH GJ, HOCKLEY AD, HAYWARD RD, DAVID DJ, PULLEYN LJ, RUTLAND P, MALCOLM S, WINTER RM, REARDON W: Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet 9:165-171, 1995.
35. YANAGISAWA M, KURIHARA H, KIMURA S, TOMOBE Y, KOBAYASHI M, MITSUI Y, YAZAKI Y, GOTO K, MASAKI T: A novel potent vasoconstrictor peptide produced by vascular endothelial cells. Nature 332:411-415, 1988.
36. YANAGISAWA H, YANAGISAWA M, KAPUR RP, RICHARDSON JA, WILLIAMS SC, CLOUTHIER DE, DEWIT D, EMOTO N, HAMMER RE: Dual genetic pathways of endothelin-mediated intercellular signaling revealed by targeted disruption of endothelin converting enzyme-1 gene. Development 125:825-836, 1998.
37. ZAIDI M, ALAM ASMT, BAX BE, SHANKAR VS, BAX CMR, GILL JS, PAZIANAS M, HUANG CLH, SAHINOGLU T, MOONGA BS, STEVENS CR, BLAKE DR: Role of the endothelial cell in osteoclast control: new perspectives. Bone 14:97-102, 1993.
38. ZOJA C, ORISIO S, PERICO N, BENIGNI A, MORIGI M, BENATTI L, RAMBALDI A, REMUZZI G: Constitutive expression of endothelin gene in cultured human mesangial cells and its modulation by transforming growth factor-β, thrombin, and a thromboxane-A2 analogue. Lab Invest 64:16-20, 1991.