Literature DB >> 1385235

Medial edge epithelium fate traced by cell lineage analysis during epithelial-mesenchymal transformation in vivo.

C F Shuler1, D E Halpern, Y Guo, A C Sank.   

Abstract

Vital cell labeling techniques were used to trace the fate of the medial edge epithelial (MEE) cells during palatal fusion in vivo. Mouse palatal tissues were labeled in utero with DiI. The fetuses continued to develop in utero and tissues of the secondary palate were examined at several later stages of palatal ontogeny. The presence and distribution of DiI was correlated with the presence of cell phenotype-specific markers. During the initial stages of palatal fusion the DiI-labeled MEE were present in the midline position. These cells were attached to an intact laminin-containing basement membrane and contained keratin intermediate filaments. At later stages of palatogenesis the DiI-labeled MEE were not separated from the mesenchyme by an intact basement membrane and did not contain keratin. In late fetal development, DiI-labeled cells without an epithelial morphology were present in the mesenchyme. The transition of the DiI-labeled cells from an epithelial phenotype to a mesenchymal phenotype is consistent with a fate of epithelial-mesenchymal transformation rather than programmed cell death.

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Year:  1992        PMID: 1385235     DOI: 10.1016/0012-1606(92)90071-n

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  30 in total

1.  TGF-beta3-induced palatogenesis requires matrix metalloproteinases.

Authors:  L Blavier; A Lazaryev; J Groffen; N Heisterkamp; Y A DeClerck; V Kaartinen
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

2.  MiR-200b is involved in Tgf-β signaling to regulate mammalian palate development.

Authors:  Jeong-Oh Shin; Jong-Min Lee; Kyoung-Won Cho; Sungwook Kwak; Hyuk-Jae Kwon; Min-Jung Lee; Sung-Won Cho; Kye-Seong Kim; Han-Sung Jung
Journal:  Histochem Cell Biol       Date:  2011-11-10       Impact factor: 4.304

3.  Induction of palate epithelial mesenchymal transition by transforming growth factor β3 signaling.

Authors:  Azadeh Jalali; Xiujuan Zhu; ChangChih Liu; Ali Nawshad
Journal:  Dev Growth Differ       Date:  2012-07-08       Impact factor: 2.053

Review 4.  Development of the upper lip: morphogenetic and molecular mechanisms.

Authors:  Rulang Jiang; Jeffrey O Bush; Andrew C Lidral
Journal:  Dev Dyn       Date:  2006-05       Impact factor: 3.780

5.  PI-3 kinase activity is required for epithelial-mesenchymal transformation during palate fusion.

Authors:  Pei Kang; Kathy K H Svoboda
Journal:  Dev Dyn       Date:  2002-11       Impact factor: 3.780

6.  miR-200b regulates cell migration via Zeb family during mouse palate development.

Authors:  Jeong-Oh Shin; Eizo Nakagawa; Eun-Jung Kim; Kyoung-Won Cho; Jong-Min Lee; Sung-Won Cho; Han-Sung Jung
Journal:  Histochem Cell Biol       Date:  2012-01-20       Impact factor: 4.304

Review 7.  Recent insights into the morphological diversity in the amniote primary and secondary palates.

Authors:  John Abramyan; Joy Marion Richman
Journal:  Dev Dyn       Date:  2015-09-10       Impact factor: 3.780

8.  TGFbeta3 inhibits E-cadherin gene expression in palate medial-edge epithelial cells through a Smad2-Smad4-LEF1 transcription complex.

Authors:  Ali Nawshad; Damian Medici; Chang-Chih Liu; Elizabeth D Hay
Journal:  J Cell Sci       Date:  2007-05-01       Impact factor: 5.285

9.  Cleft lip and palate genetics and application in early embryological development.

Authors:  Wenli Yu; Maria Serrano; Symone San Miguel; L Bruno Ruest; Kathy K H Svoboda
Journal:  Indian J Plast Surg       Date:  2009-10

10.  Integration of IRF6 and Jagged2 signalling is essential for controlling palatal adhesion and fusion competence.

Authors:  Rebecca J Richardson; Jill Dixon; Rulang Jiang; Michael J Dixon
Journal:  Hum Mol Genet       Date:  2009-05-13       Impact factor: 6.150

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