Snail family members and cell survival in physiological and pathological cleft palates

Developmental Biology

Volumn 265, Issue 1, 2004, Pages 207-218

  Martínez Álvarez, Concepción ^a   Blanco, María J ^a,b   Pérez, Raquel ^a   Rabadán, M Angeles ^a   Aparicio, Marta ^a   Resel, Eva ^a   Martínez, Tamara ^a   Nieto, M Angela ^b  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b INSTITUTO CAJAL   (Spain)

Author keywords

Cell death; Chick; Epithelial mesenchymal transition; Mouse; Palate development; Slug; Snail; Survival; TGF 1; TGF 3

Indexed keywords

TRANSFORMING GROWTH FACTOR BETA1; TRANSFORMING GROWTH FACTOR BETA3;

ANIMAL CELL; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL FUSION; CELL MUTANT; CELL SUBPOPULATION; CELL SURVIVAL; CLEFT PALATE; CONTROLLED STUDY; EMBRYO; EMBRYO DEVELOPMENT; EPITHELIUM CELL; GENE ACTIVATION; GENE CONTROL; GENE EXPRESSION REGULATION; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MESENCHYME; MOUSE; MULTIGENE FAMILY; NONHUMAN; PATHOGENESIS; PRIORITY JOURNAL; REGULATOR GENE; SLUG GENE; SNAIL GENE; TISSUE CULTURE; UPREGULATION; WILD TYPE;

AVES; GASTROPODA; MAMMALIA;

EID: 0345731233     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2003.09.022     Document Type: Article

References (58)

1. Aybar M., Nieto M.A., Mayor R. Snail precedes Slug in the genetic cascade required for the specification and migration of the Xenopus neural crest. Development. 130:2003;483-494.
2. Batlle E., Sancho E., Franci C., Dominguez D., Monfar M., Baulida J., Garcia De Herreros A. The transcription factor Snail is a repressor of E-cadherin gene expression in epithelial tumour cells. Nat. Cell Biol. 2:2000;84-89.
3. Blanco M.J., Moreno-Bueno G., Sarrio D., Locascio A., Cano A., Palacios J., Nieto M.A. Correlation of Snail expression with histological grade and lymph node status in breast carcinomas. Oncogene. 21:2002;3241-3246.
4. Buxton P.G., Kostakopoulou K., Brickell P., Thorogood P., Ferretti P. Expression of the transcription factor Slug correlates with growth of the limb bud and is regulated by FGF-4 and retinoic acid. Int. J. Dev. Biol. 41:1997;559-568.
5. Cano A., Pérez M.A., Rodrigo I., Locascio A., Blanco M.J., Del Barrio M.G., Portillo F., Nieto M.A. The transcription factor Snail controls epithelial-mesenchymal transitions by repressing E-cadherin expression. Nat. Cell Biol. 2:2000;76-83.
6. Carette M.J.M., Ferguson M.W.J. The fate of medial epithelial cells during palatal fusion in vitro: an analysis by DiI labelling and confocal microscopy. Development. 114:1992;379-388.
7. Carl T.F., Dufton C., Hanken J., Klymkowsky M.W. Inhibition of neural crest migration in Xenopus using antisense slug RNA. Dev. Biol. 213:1999;101-115.
8. Carver E.A., Jiang R., Lan Y., Oram K.F., Gridley T. The mouse Snail gene encodes a key regulator of the epithelial-mesenchymal transition. Mol. Cell. Biol. 21:2001;8184-8188.
9. Cuervo R., Valencia C., Chandraratna R.A., Covarrubias L. Programmed cell death is required for palate shelf fusion and is regulated by retinoic acid. Dev. Biol. 245:2002;145-156.
10. Cui X.M., Wartburton D., Zho J., Crowe D.L., Shuler C.F. Immunohistochemical localization of TGF-beta type II receptor and TGF-beta3 during palatogenesis in vivo and in vitro. Int. J. Dev. Biol. 42:1998;817-820.
11. Cui X.M., Chai Y., Chen J., Yamamoto T., Ito Y., Bringas P., Shuler C.F. TGF-beta3-dependent SMAD2 phosphorylation and inhibition of MEE proliferation during palatal fusion. Dev. Dyn. 227:2003;387-394.
12. Del Barrio M.G., Nieto M.A. Overexpression of Snail family members highlights their ability to promote chick neural crest formation. Development. 129:2002;1583-1593.
13. Dickinson M.E., Selleck M.A., McMahon A.P., Bronner-Fraser M. Dorsalization of the neural tube by the non-neural ectoderm. Development. 121:1995;2099-2106.
14. Ferguson M.W.J. Palate development. Development. 103:1988;41-60. (Suppl.).
15. Fitchett J.E., Hay E.D. Medial edge epithelium transforms to mesenchyme after embryonic palatal shelves fuse. Dev. Biol. 131:1989;455-474.
16. Gato A., Martinez M.L., Tudela C., Alonso I., Moro J.A., Formoso M.A., Ferguson M.W.J., Martínez-Álvarez C. TGF-β-induced chondroitin sulphate proteoglycan mediates palatal shelf adhesion. Dev. Biol. 250:2002;393-405.
17. Gehris A.L., D'Angelo M., Greene R.M. Immunodetection of the transforming growth factor β1 and β2 in the developing murine palate. Int. J. Dev. Biol. 35:1991;17-24.
18. Gotzmann J., Huber H., Thallinger C., Wolschek M., Jansen B., Schulte-Hermann R., Beug H., Mikulits W. Hepatocytes convert to a fibroblastoid phenotype through the cooperation of TGF-beta1 and Ha-Ras: steps towards invasiveness. J. Cell Sci. 115:2002;1189-1202.
19. Graham A., Francis-West P., Brickell P., Lumsden A. The signalling molecule BMP4 mediates apoptosis in the rhombencephalic neural crest. Nature. 372:1994;684-686.
20. Griffith C.M., Hay E.D. Epithelial-mesenchymal transformation during palatal fusion: carboxyfluorescein traces cells at light and electron microscopic levels. Development. 116:1992;1099-1987.
21. Hamburger V., Hamilton H. A series of normal stages in the development of the chick embryo. J. Morphol. 88:1951;49-92.
22. Inoue A., Seidel M.G., Wu W., Kamizono S., Ferrando A.A., Bronson R.T., Iwasaki H., Akashi K., Morimoto A., Hitzler J.K., Pestina T.I., Jackson C.W., Tanaka R., Chong M.J., McKinnon P.J., Inukai T., Grosveld G.C., Look A. Slug, a highly conserved zinc finger transcriptional repressor, protects hematopoietic progenitor cells from radiation-induced apoptosis in vivo. Cancer Cells. 2:2002;279-288.
23. Inukai T., Inoue A., Kurosawa H., Goi K., Shinjyo T., Ozawa K., Mao M., Inaba T., Look A.T. Slug, a ces-1-related zinc finger transcription factor gene with antiapoptotic activity is a downstream target of the E2A-HLF oncoprotein. Mol. Cell. 4:1999;343-352.
24. 3 indicates defects of epithelial-mesenchymal interaction. Nat. Genet. 11:1995;415-421.
25. Kaartinen V., Cui X.M., Heisterkamp N., Groffen J., Shuler C.F. Transforming growth factor-β3 regulates transdifferentiation of medial edge epithelium during palatal fusion and associated degradation of the basement membrane. Dev. Dyn. 209:1997;255-260.
26. LaBonne C., Bronner-Fraser M. Snail-related transcriptional repressors are required in Xenopus both for induction of the neural crest and its subsequent migration. Dev. Biol. 221:2000;195-205.
27. 3 with nonsyndromic clefting in humans. Am. J. Hum. Genet. 63:1998;557-568.
28. Liem K.F.Jr., Tremml G., Roelink H., Jessell T. Dorsal differentiation of neural plate cells induced by BMP-mediated signals from epidermal ectoderm. Cell. 82:1995;969-979.
29. Locascio A., Manzanares M., Blanco M.J., Nieto M.A. Modularity and reshuffling of Snail and Slug expression during vertebrate evolution. Proc. Natl. Acad. Sci. U. S. A. 99:2002;16841-16846.
30. Martínez-Álvarez C., Tudela C., Pérez-Miguelsanz J., O'Kane S., Puerta J., Ferguson M.W.J. Medial edge epithelial cell fate during palatal fusion. Dev. Biol. 220:2000;343-357.
31. Martínez-Álvarez C., Bonelli R., Tudela C., Gato A., Mena J., O'Kane S., Ferguson M.W.J. Bulging medial edge epithelial cells and palatal fusion. Int. J. Dev. Biol. 44:2000;331-335.
32. Metzstein M.M., Horwitz H.R. The C. elegans cell death specification gene ces-1 encodes a Snail family zinc finger protein. Mol. Cell. 4:1999;309-319.
33. Mori C., Nakamura N., Okamoto Y., Osawa M., Shiota K. Cytochemical identification of programmed cell death in the fusing fetal mouse palate by specific labeling of DNA fragmentation. Anat. Embryol. 190:1994;21-28.
34. Motyl T., Grzelkowska K., Zimowska W., Skierski J., Wareski P., Ploszaj T., Trzeciak L. Expression of bcl-2 and bax in TGF-beta 1-induced apoptosis of L1210 leukemic cells. Eur. J. Cell Biol. 75:1998;367-374.
35. Nieto M.A. The early steps of neural crest development. Mech. Dev. 105:2001;27-35.
36. Nieto M.A. The Snail superfamily of zinc finger transcription factors. Nat. Rev., Mol. Cell Biol. 3:2002;155-166.
37. Nieto M.A., Bennet M.F., Sargent M.G., Wilkinson D.G. Cloning and developmental expression of Sna, a murine homologue of the Drosophila snail gene. Development. 116:1992;227-237.
38. Nieto M.A., Sargent M., Wilkinson D.G., Cooke J. Control of cell behavior during vertebrate development by Slug, a zinc-finger gene. Science. 264:1994;836-840.
39. Nieto M.A., Patel K., Wilkinson D.G. In situ hybridisation analysis of chick embryos in whole mount and tissue sections. Methods Cell Biol. 51:1996;220-235.
40. Oberhammer F.A., Pavelka M., Sharma S., Tiefenbacher R., Purchio A.F., Bursch W., Schulte-Hermann R. Induction of apoptosis in cultures hepatocytes and in regressing liver by transforming growth factor β1. Proc. Natl. Acad. Sci. U. S. A. 89:1992;5408-5412.
41. Perez-Losada J., Sanchez-Martin M., Perez-Caro M., Perez-Mancera P.A., Sánchez-Garcia I. The radioresistance biological function of the SCF/kit signaling pathway is mediated by the zinc-finger transcription factor Slug. Oncogene. 22:2003;4205-4211.
42. Piedra M.E., Ros M.A. BMP signaling positively regulates Nodal expression during left right specification in the chick embryo. Development. 129:2002;3431-3440.
43. 3 is required for secondary palate fusion. Nat. Genet. 11:1995;409-414.
44. Romano L., Runyan R.B. Slug is and essential target of TGFβ2 signaling in the developing chicken heart. Dev. Biol. 223:2000;91-102.
45. Ros M., Sefton M., Nieto M.A. Slug, a zinc finger gene previously implicated in the early patterning of the mesoderm and the neural crest, is also involved in chick limb development. Development. 124:1997;1821-1829.
46. Sánchez A., Alvarez A.M., Benito M., Fabregat I. Apoptosis induced by transforming growth factor-β in fetal hepatocytes primary cultures. J. Biol. Chem. 271:1996;7416-7422.
47. Sefton M., Sanchez S., Nieto M.A. Conserved and divergent roles for members of the Snail family of transcription factors in the chick and mouse embryo. Development. 125:1998;3111-3121.
48. Shabana A.H., Ouhayoun J.P., Sawaf M.H., Forest M. Cytokeratin patterns of human oral mucosae in histiotypic culture. Arch. Oral Biol. 36:1991;747-758.
49. 3 to cutaneous rat wounds reduces scarring. J. Cell Sci. 108:1995;985-1002.
50. Shin I., Bakin A.V., Rodeck U., Brunet A., Arteaga C.L. Transforming growth factor β enhances epithelial cell survival via AKT-dependent regulation of FKHRL1. Mol. Biol. Cell. 12:2001;3328-3339.
51. Shuler C.F., Halpern D.E., Guo Y., Shank C. Medial edge epithelium fate by cell lineage analysis during epithelial-mesenchymal transformation in vivo. Dev. Biol. 154:1992;318-330.
52. Smith D.E., Franco del Amo M., Gridley T. Isolation of Sna, a mouse gene homologue to the Drosophila genes snail and escargot: its expression pattern suggests multiple roles during postimplantation development. Development. 116:1992;1033-1039.
53. Spagnoli F.M., Cicchini C., Tripodi M., Weiss M.C. Inhibition of MMH (Met murine hepatocyte) cell differentiation by TGF-β is abrogated by pretreatment with the inheritable differentiation factor FGF1. J. Cell Sci. 113:2000;3639-3647.
54. Sun D., Vanderburg C.R., Odierna G.S., Hay E.D. TGFβ3 promotes transformation of chicken palate medial edge epithelium to mesenchyme in vitro. Development. 125:1998;95-105.
55. Taniguchi K., Sato N., Uchiyama Y. Apoptosis and heterophagy of medial edge epithelial cells of the secondary palatine shelves during fusion. Arch. Histol. Cytol. 58:1995;191-203.
56. Taya Y., O'Kane S., Ferguson M.W.J. Pathogenesis of cleft palate in TGF-β knockout mice. Development. 126:1999;3869-3879.
57. 3 is required for the adhesion and intercalation of medial edge epithelial cells during palate fusion. Int. J. Dev. Biol. 46:2002;333-336.
58. Valdés F., Álvarez A.M., Locascio A., Vega S., Herrera B., Fernández M., Benito M., Nieto M.A., Fabregat I. The epithelial mesenchymal transition confers resistance to the apoptotic effects of TGF-β in fetal rat hepatocytes. Mol. Cancer Res. 1:2002;68-78.