Literature DB >> 1801871

Molecular and morphologic changes during the epithelial-mesenchymal transformation of palatal shelf medial edge epithelium in vitro.

C F Shuler1, Y Guo, A Majumder, R Y Luo.   

Abstract

The fate of the medial edge epithelial (MEE) cells during palatal fusion has been proposed to be either programmed cell death or epithelial-mesenchymal transformation. Vital cell labeling techniques were used to mark the MEE and observe their fate during palatal fusion in vitro. Fetal mouse palatal shelves were labeled with Dil and allowed to proceed through fusion while maintained in an organ culture system. The tissues were examined at several stages of palatal fusion for the distribution of Dil, presence of specific antigens and ultrastructural appearance of the cells. The MEE labeled with Dil occupied a midline position at all stages of palatal fusion. Initially the cells had keratin intermediate filaments and were separated from the underlying mesenchyme by an intact basement membrane. During the process of fusion the basement membrane was degraded and the Dil-labeled MEE were in contact with the mesenchymal-derived extracellular matrix. In the late stages of fusion the Dil-labeled MEE altered their cellular morphology, had vimentin intermediate filaments, and were not associated with an identifiable basement membrane. Dil-labeled cells, without an epithelial phenotype, remained present in the midline of the completely fused palate. The data indicate that the MEE did not die but underwent a phenotypic transformation to viable mesenchymal cell types, which were retained in the palatal mesenchyme.

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Year:  1991        PMID: 1801871

Source DB:  PubMed          Journal:  Int J Dev Biol        ISSN: 0214-6282            Impact factor:   2.203


  16 in total

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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
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Review 3.  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

4.  Spatiotemporal localization of periostin and its potential role in epithelial-mesenchymal transition during palatal fusion.

Authors:  Yukiko Kitase; Keisuke Yamashiro; Katherine Fu; Joy M Richman; Charles F Shuler
Journal:  Cells Tissues Organs       Date:  2010-11-03       Impact factor: 2.481

Review 5.  Palate morphogenesis: current understanding and future directions.

Authors:  Robert M Greene; M Michele Pisano
Journal:  Birth Defects Res C Embryo Today       Date:  2010-06

6.  The expression of TGF-β3 for epithelial-mesenchyme transdifferentiated MEE in palatogenesis.

Authors:  Akira Nakajima; Eiji Tanaka; Yoshihiro Ito; Masao Maeno; Koichi Iwata; Noriyoshi Shimizu; Charles F Shuler
Journal:  J Mol Histol       Date:  2010-10-22       Impact factor: 2.611

7.  Expression of Wnts in the developing murine secondary palate.

Authors:  Dennis R Warner; Henry S Smith; Cynthia L Webb; Robert M Greene; M Michele Pisano
Journal:  Int J Dev Biol       Date:  2009       Impact factor: 2.203

Review 8.  Palatal seam disintegration: to die or not to die? that is no longer the question.

Authors:  Ali Nawshad
Journal:  Dev Dyn       Date:  2008-10       Impact factor: 3.780

9.  Nicotine inhibits palatal fusion and modulates nicotinic receptors and the PI-3 kinase pathway in medial edge epithelia.

Authors:  P Kang; K K H Svoboda
Journal:  Orthod Craniofac Res       Date:  2003-08       Impact factor: 1.826

10.  Functional role of TGF-β receptors during palatal fusion in vitro.

Authors:  Akira Nakajima; Yoshihiro Ito; Eiji Tanaka; Remi Sano; Yoko Karasawa; Masao Maeno; Koichi Iwata; Noriyoshi Shimizu; Charles F Shuler
Journal:  Arch Oral Biol       Date:  2014-07-24       Impact factor: 2.633

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