1997
DOI: 10.1002/(sici)1097-0177(199704)208:4<526::aid-aja8>3.0.co;2-k
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Characterization of the fate of midline epithelial cells during the fusion of mandibular prominences in vivo

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Cited by 25 publications
(13 citation statements)
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“…Our microarray data also showed that the EMT-inducible transcription factor Snai1 and the Rho family (Rhoa, Rac1, and Cdc42) were either constitutive or L region-specific (data not shown). Taken with the report that knockout mice lacking Igfbp5 expression grow without defects in the orofacial architecture (Ning et al, 2006), we speculate that Igfbp5 localized in the mandibular epithelium may contribute to modulation in fine-tune of the epithelial integrity before the midline epithelium becomes ultimately incorporated within the oral epithelia covering the mandible (Chai, 1997). In connection with the epithelium-dominant Igfbp5 expression, the present IPA results indicated that Igfbp5 is a downstream target of Shh expressed exclusively in the M1-epi (Fig.…”
Section: Ipa Prediction Of Upstream Regulators Of Medial Region-specisupporting
confidence: 83%
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“…Our microarray data also showed that the EMT-inducible transcription factor Snai1 and the Rho family (Rhoa, Rac1, and Cdc42) were either constitutive or L region-specific (data not shown). Taken with the report that knockout mice lacking Igfbp5 expression grow without defects in the orofacial architecture (Ning et al, 2006), we speculate that Igfbp5 localized in the mandibular epithelium may contribute to modulation in fine-tune of the epithelial integrity before the midline epithelium becomes ultimately incorporated within the oral epithelia covering the mandible (Chai, 1997). In connection with the epithelium-dominant Igfbp5 expression, the present IPA results indicated that Igfbp5 is a downstream target of Shh expressed exclusively in the M1-epi (Fig.…”
Section: Ipa Prediction Of Upstream Regulators Of Medial Region-specisupporting
confidence: 83%
“…On the other hand, in the primary palatogenesis, epithelial fusion between the lateral-nasal and maxillary prominences begins in a small area and pressure from growth in the apposed mesenchyme subsequently pushes out the intervening epithelium (Minkof, 1980;Bailey et al, 1988;Diewert and Wang, 1992). This is also the case for the fusion of the mandibular prominences and the epithelial cells become incorporated within the oral epithelia that ultimately cover the mandible (Chai et al, 1997). This sequence of fusion events was originally described as a 'merging' (Patten, 1961).…”
Section: Introductionmentioning
confidence: 97%
“…Mandibular development depends upon the interaction between the oral ectoderm and the CNC-derived mesenchyme within the first branchial arch. Within the oral ectoderm, signaling molecules, such as BMP, TGF-␤, and FGF, are expressed in a region-specific manner (Chai et al, 1994(Chai et al, , 1997Trumpp et al, 1999;Ito et al, 2002;Liu et al, 2005). They may regulate homeobox-containing genes (such as Dlx, Lhx, and Gsc) within the CNC-derived mesenchyme to generate early polarity and are responsible for patterning of the first branchial arch.…”
Section: Mandibular Morphogenesismentioning
confidence: 99%
“…The mechanisms for removal of the epithelial cells that results in mesenchymal continuity in facial processes are thought to be mediated by either programmed cell death (apoptosis), epithelial-mesenchymal transformation, or migration to adjacent epithelia (Shuler, 1995 epithelial cell migration (Shuler et al, 1992;Shuler, 1995;Chai et al, 1997;McGonnell et al, 1998). Studies in the mouse embryo indicate that merger of the 2 mandibular processes starts at E9.5 and is completed within 24 to 36 hrs at Ell (Chai et al, 1997). During this process, the epithelium covering the tips of the mandibular processes consists of 2 cell layers that adhere to each other and subsequently fuse to form an epithelial seam about 3 or 4 cell layers thick.…”
Section: Epidermal Growth Factor (Egf)mentioning
confidence: 99%